The DOI matches its Crossref record; 109 of the 110 references it cites were found in a registry or an index; 62 of the 157 sources its claims cite were checked for support.
Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function
Open accessAbstract
Neural circuits must maintain stable function in the face of many plastic challenges, including changes in synapse number and strength, during learning and development. Recent work has shown that these destabilizing influences are counterbalanced by homeostatic plasticity mechanisms that act to stabilize neuronal and circuit activity. One such mechanism is synaptic scaling, which allows neurons to detect changes in their own firing rates through a set of calcium-dependent sensors that then regulate receptor trafficking to increase or decrease the accumulation of glutamate receptors at synaptic sites. Additional homeostatic mechanisms may allow local changes in synaptic activation to generate local synaptic adaptations, and network-wide changes in activity to generate network-wide adjustments in the balance between excitation and inhibition. The signaling pathways underlying these various forms of homeostatic plasticity are currently under intense scrutiny, and although dozens of molecular pathways have now been implicated in homeostatic plasticity, a clear picture of how homeostatic feedback is structured at the molecular level has not yet emerged. On a functional level, neuronal networks likely use this complex set of regulatory mechanisms to achieve homeostasis over a wide range of temporal and spatial scales.
Overview
AI snapshot
Written from the paper’s full text.
TL;DR
Homeostatic synaptic plasticity stabilizes neuronal firing through mechanisms such as synaptic scaling, which uses calcium-dependent sensors to bidirectionally regulate glutamate receptor accumulation at synapses. The review distinguishes global, cell-autonomous scaling from local/quasi-local and network-level mechanisms, and highlights that the molecular logic of homeostatic feedback remains incompletely understood.
Key findings
- Synaptic scaling is a cell-autonomous, global form of homeostatic plasticity: perturbing activity bidirectionally scales quantal amplitude (mEPSC/mini amplitude) up or down, regulating both AMPA and NMDA currents proportionally, and requires the GluA2 subunit of AMPARs.
- Scaling up and scaling down share some calcium/CaMKK/CaMKIV signaling but diverge in other molecular requirements; for example, scaling up depends completely on PSD-95, whereas scaling down can be supported by either PSD-95 or PSD-93.
- Local or quasi-local homeostatic mechanisms also exist: combined TTX and glutamate receptor block locally enhances GluA1-containing/GluA2-lacking AMPAR insertion via retinoic acid/RARα, and presynaptic release probability can be regulated quasi-locally by dendritic depolarization.
- Network-level and secreted-factor mechanisms contribute to excitation/inhibition balance: BDNF and glial TNFα are implicated, with TNFα suggested to be permissive/maintenance rather than instructive for scaling; in vivo visual deprivation can scale mEPSC amplitude and insert GluA2-containing AMPARs.
Methods
- This is a review article, not a primary experimental study; it synthesizes findings from in vitro and in vivo work on homeostatic synaptic plasticity at the neuromuscular junction and central mammalian synapses.
- The paper reviews signaling pathways, expression mechanisms, and functional roles of synaptic scaling, local/quasi-local plasticity, secreted factors, and synapse-type-specific rules.
- No new experimental sample, dataset, or statistical analysis is reported.
Limitations
- Stated: the signaling pathways underlying homeostatic plasticity are under intense scrutiny, but “a clear picture of how homeostatic feedback is structured at the molecular level has not yet emerged.”
- Stated: whether mechanisms underlying synaptic scaling in vivo and in other brain regions are similar to or distinct from those in cultured cortical neurons remains an open question.
- Stated: local homeostatic regulation remains controversial, and the physiological significance of some presynaptic changes, such as VGlut changes, remains to be determined. Evident: as a narrative review, it does not systematically quantify evidence or resolve conflicting findings across studies.
Model-written summary. Check it against the paper before relying on it.
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Claims the paper makes
62 of 157 cited sources checked · 34 supported · 2 flagged · accuracy not yet measured
At least one cited source doesn’t support this claim or points to a different paper, and none confirmed it — see the verdicts below.
In the paper
“However, scaling up can also be induced by chronic changes in the level of depolarization in a BDNF-independent manner (Leslie et al. 2001), and the relationship between BDNF-mediated synaptic scaling and cell-autonomous synaptic scaling of excitatory inputs (Ibata et al. 2008) remains unclear.”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > ROLE OF NETWORK ACTIVITY AND SECRETED FACTORS IN THE INDUCTION OF HOMEOSTATIC PLASTICITY
What the sources say
- Disputedcites Leslie et al. 2001 sourceExperimental — accuracy not yet measured
The Abstract (page unavailable) says chronic depolarization reduced excitatory quantal amplitude in a BDNF-independent manner—the opposite of scaling up. It attributes scaling up to low levels of BDNF, and the Discussion likewise distinguishes the BDNF-dependent increase from the depolarization-induced decrease. (LLM, conf=0.94)
Checked by a reasoning model — may be wrong.
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passes- Disputed
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Central neurons are embedded in complex networks composed of many cell types, including both excitatory and inhibitory neurons, and small changes in the balance between excitation and inhibition can have major effects on ongoing activity (Nelson and Turrigiano 2008).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > HOMEOSTATIC PLASTICITY AT CENTRAL MAMMALIAN SYNAPSES
What the sources say
- Partly supportedcites Nelson and Turrigiano 2008 sourceExperimental — accuracy not yet measured
The Inhibitory Plasticity section discusses balancing excitation and inhibition, and the Homeostatic Plasticity section says changes in synaptic strength can alter neuronal activity. The copy does not establish the more specific claim that small shifts in excitation–inhibition balance have major effects on ongoing activity. Page numbers are unavailable in our copy. (LLM, conf=0.78)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“where it was observed that loss of synaptic innervation initiated an increase in muscle excitability through changes in postsynaptic receptor number and localization.”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > HOMEOSTATIC PLASTICITY AT THE NEUROMUSCULAR JUNCTION
What the sources say
- Partly supportedcites Berg and Hall, 1975 sourceExperimental — accuracy not yet measured
The Abstract reports that chronic neuromuscular blockade increased extrajunctional acetylcholine-receptor binding and sensitivity in rat muscle, with changes similar to those after denervation. But the nerve remained active during blockade, so the paper does not establish that loss of synaptic innervation initiated the change or that receptor changes caused increased muscle excitability. (LLM, conf=0.84)
- Not checked — no full text of the sourcecites Sharpless 1975
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passes- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“One such mechanism is synaptic scaling, which allows neurons to detect changes in their own firing rates through a set of calcium-dependent sensors that then regulate receptor trafficking to increase or decrease the accumulation of glutamate receptors at synaptic sites.”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > Abstract
What the sources say
- Not checked — no full text of the sourcecites Turrigiano et al. 1998 source
- Partly supportedcites Gainey et al. 2009 sourceExperimental — accuracy not yet measured
The Introduction says that a drop in postsynaptic firing leads to AMPA-receptor accumulation at synapses, and the Discussion describes synaptic strengths scaling up or down in response to chronic changes in activity. The paper also links scaling to receptor trafficking, but the passages do not identify calcium-dependent sensors that detect firing-rate changes or regulate that trafficking. Page numbers are unavailable in our copy. (LLM, conf=0.86)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesThe cited sources support only part of this claim — read each source’s verdict below.
In the paper
“One interesting implication of this model is that the firing rate set point is an emergent property that represents the stable point of all the opposing signaling pathways that operate on synaptic strength (Turrigiano 2008).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CELL-AUTONOMOUS, GLOBAL SYNAPTIC SCALING OF EXCITATORY SYNAPSES
What the sources say
- Partly supportedcites Turrigiano 2008 sourceExperimental — accuracy not yet measured
In Concluding Remarks, the paper proposes that the activity set point could arise where opposing forces regulating receptor accumulation equalize. The citing sentence presents this proposed model as fact and extends it to all opposing signaling pathways that affect synaptic strength, which the passage does not establish. (LLM, conf=0.87)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passes- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“This global enhancement of AMPAR abundance in response to activity blockade requires sequences on the carboxyl terminus of the GluA2 subunit of the AMPAR (Gainey et al. 2009)”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CELL-AUTONOMOUS, GLOBAL SYNAPTIC SCALING OF EXCITATORY SYNAPSES
What the sources say
- Supportedcites Gainey et al. 2009 source
The Results section, “The GluR2 C-Tail is required for the expression of synaptic scaling” (page unavailable), reports that replacing the GluR2 C-tail with the GluR1 C-tail blocks synaptic scaling. The Discussion explicitly concludes that regulatory sequences on the GluR2 (GluA2) C-tail are required for TTX-induced AMPAR accumulation. (LLM, conf=0.94)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes- Supported
The sources with a verdict support this claim; the rest weren’t checked yet, have no full text we could read, or their verdicts aren’t rated yet.
In the paper
“the majority of studies that have blocked activity with tetrodotoxin (TTX) or AMPAR antagonists have observed a coordinated increase in GluA1 and GluA2 (O'Brien et al. 1998;Wierenga et al. 2005;Cingolani et al. 2008;Sun and Wolf 2009;Anggono et al. 2011; but see Thiagarajan et al. 2005).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CELL-AUTONOMOUS, GLOBAL SYNAPTIC SCALING OF EXCITATORY SYNAPSES
What the sources say
- Not checked — no full text of the sourcecites O'Brien et al. 1998 source
- Supportedcites Wierenga et al. 2005 source
The Results section, “Effect of activity blockade on cell-surface GluR1 and GluR2,” reports that TTX treatment increased synaptic GluR1 and GluR2 accumulation proportionally in cultured neocortical neurons. This supports citing the study as an example of a coordinated increase; it does not need to establish the collective claim about the majority of studies on its own. (LLM, conf=0.93)
- Not checked — no full text of the sourcecites Cingolani et al. 2008 source
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesThe cited sources support only part of this claim — read each source’s verdict below.
In the paper
“by measuring minis arising from many synapses onto the same neuron, it was observed that modulating network activity induced uniform increases or decreases in the entire mini amplitude distribution, in effect scaling postsynaptic strength up or down (Turrigiano et al. 1998;Desai et al. 2002;Gainey et al. 2009).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CELL-AUTONOMOUS, GLOBAL SYNAPTIC SCALING OF EXCITATORY SYNAPSES
What the sources say
- Not checked — no full text of the sourcecites Turrigiano et al. 1998 source
- Not checked — no full text of the sourcecites Desai et al. 2002 source
- Partly supportedcites Gainey et al. 2009 sourceExperimental — accuracy not yet measured
The Results section ('GluR2 knockdown blocks synaptic scaling, but does not block LTP'; page not provided) reports that activity blockade proportionally scaled up the mEPSC amplitude distribution. The copy does not report a corresponding activity-induced decrease across that distribution. Its reference to scaling a distribution down describes a mathematical comparison with controls, not a physiological decrease in postsynaptic strength. (LLM, conf=0.86)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesEvery source the paper cites for this claim was checked and supports it.
In the paper
“On the presynaptic side, there is compelling evidence that homeostatic modulation of neurotransmitter release probability (P r ) can happen at the level of individual dendritic branches.”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > LOCAL AND QUASI-LOCAL FORMS OF HOMEOSTATIC SYNAPTIC PLASTICITY IN CENTRAL NEURONS
What the sources say
- Supportedcites Branco et al. 2008 source
The Introduction reports that release probability homeostatically adapts to the number of synapses on a dendritic branch and to selective increases in postsynaptic activity. The Discussion adds that selectively stimulating a small group of synapses caused a compensatory decrease confined to the stimulated area, supporting local modulation at or below the branch level. (LLM, conf=0.93)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“It is widely agreed that synaptic scaling involves postsynaptic changes in receptor accumulation (Turrigiano 2008), but under some circumstances additional presynaptic changes can also be recruited (Davis and Bezprozvanny 2001;Rich and Wenner 2007;Thiagarajan et al. 2007).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CELL-AUTONOMOUS, GLOBAL SYNAPTIC SCALING OF EXCITATORY SYNAPSES
What the sources say
- Supportedcites Turrigiano 2008 source
In “Homeostatic Regulation of AMPA Receptor Trafficking,” the review states that there is consensus that changes in postsynaptic receptor accumulation are a major expression mechanism of synaptic scaling. This directly supports the claim attributed to Turrigiano (2008). (LLM, conf=0.95)
Strength:boosted· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passes- Supported
- It may state two separate claims as one. 41
- Probably not a substantial claim. 8
At least one cited source doesn’t support this claim or points to a different paper, and none confirmed it — see the verdicts below.
In the paper
“Further, whereas scaling up is completely dependent on the scaffold protein PSD-95, scaling down can be supported by either PSD-95 or PSD-93 (Sun and Turrigiano 2011).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CELL-AUTONOMOUS, GLOBAL SYNAPTIC SCALING OF EXCITATORY SYNAPSES
What the sources say
- Disputedcites Sun and Turrigiano 2011 sourceExperimental — accuracy not yet measured
The Discussion states the reverse: scaling down is critically dependent on PSD-95, while scaling up can be supported by either PSD-95 or PSD-93 in young neurons. The Results section ‘PSD-95 is necessary for scaling down’ likewise says PSD-93 cannot compensate for loss of PSD-95 during scaling down. The paper adds that scaling up becomes dependent on PSD-95 in older neurons. (LLM, conf=0.90)
Checked by a reasoning model — may be wrong.
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Disputed
Every source the paper cites for this claim was checked and supports it.
In the paper
“It is worth noting, however, that postsynaptic knockdown of GluA2 is able to completely block synaptic scaling (Gainey et al. 2009), suggesting that if there is a presynaptic change in transmitter packaging it is not sufficient to enhance mini amplitude on its own.”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CELL-AUTONOMOUS, GLOBAL SYNAPTIC SCALING OF EXCITATORY SYNAPSES
What the sources say
- Supportedcites Gainey et al. 2009 source
The Results section (‘GluR2 knockdown blocks synaptic scaling, but does not block LTP’) reports that TTX increased mEPSC amplitude in control neurons but not in GluR2-knockdown neurons. The Discussion explicitly says the knockdown completely blocked synaptic scaling. The statement about presynaptic transmitter packaging is the citing authors’ inference, not a separate finding attributed to this source. (LLM, conf=0.94)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Supported
The sources with a verdict support this claim; the rest weren’t checked yet, have no full text we could read, or their verdicts aren’t rated yet.
In the paper
“Given that the postsynaptic and presynaptic responses to activity deprivation can occur independently (Wierenga et al. 2005(Wierenga et al. , 2006)), it is likely that they represent distinct forms of plasticity induced by distinct signaling pathways.”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CELL-AUTONOMOUS, GLOBAL SYNAPTIC SCALING OF EXCITATORY SYNAPSES
What the sources say
- Supportedcites Wierenga et al. 2005 source
The Discussion states that increased postsynaptic receptor accumulation can occur without measurable changes in presynaptic function and describes the changes as separable, independent homeostatic mechanisms. The statement about distinct signaling pathways is the citing authors’ inference, not the part directly attributed to this source. (LLM, conf=0.93)
- Not checked — no full text of the sourcecites Wierenga et al. 2006 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Like scaling up, scaling down in response to elevated network activity is a cell-autonomous function of postsynaptic firing, and involves enhanced calcium influx (Fig. 2), gene transcription, the CaMKK/CaMKIV signaling pathway, and targets the GluA2 subunit (Goold and Nicoll 2010).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CELL-AUTONOMOUS, GLOBAL SYNAPTIC SCALING OF EXCITATORY SYNAPSES
What the sources say
- Partly supportedcites Goold and Nicoll 2010 sourceExperimental — accuracy not yet measured
The Discussion reports that cell-autonomous excitation drives calcium-dependent synaptic depression through CaMKK/CaMK4. It also limits the transcription and GluA2 requirements to AMPAR depression: NMDAR depression does not require them. The citing sentence omits that distinction when describing scaling down generally. (LLM, conf=0.85)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Lowering presynaptic firing with an inwardly rectifying K ir channel was observed to selectively enhance the accumulation of GluA1 at postsynaptic sites, suggesting the existence of a synapse-specific form of homeostatic compensation to reduced receptor activation (Hou et al. 2008).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > LOCAL AND QUASI-LOCAL FORMS OF HOMEOSTATIC SYNAPTIC PLASTICITY IN CENTRAL NEURONS
What the sources say
- Supportedcites Hou et al. 2008 source
Split into 2 atoms — 2 confirmed, 0 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Supported
The sources with a verdict support this claim; the rest weren’t checked yet, have no full text we could read, or their verdicts aren’t rated yet.
In the paper
“Interestingly, synaptic scaling protocols homeostatically regulate both the NMDA and the AMPA component of glutamatergic synaptic currents, and the change in AMPA and NMDA currents are proportional at individual synapses (Watt et al. 2000;Perez-Otano and Ehlers 2005).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CELL-AUTONOMOUS, GLOBAL SYNAPTIC SCALING OF EXCITATORY SYNAPSES
What the sources say
- Supportedcites Watt et al. 2000 source
The Abstract reports that long-lasting changes in activity scaled AMPA and NMDA currents up and down proportionally. It also says their ratio at different synapses onto the same neuron was preserved after scaling. The findings concern neocortical synapses expressing both receptor types. (LLM, conf=0.93)
- Not checked — no full text of the sourcecites Perez-Otano and Ehlers 2005 source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Supported
The sources with a verdict support this claim; the rest weren’t checked yet, have no full text we could read, or their verdicts aren’t rated yet.
In the paper
“Interestingly, the same manipulation (activity blockade using TTX or AMPAR antagonists) that only affects mini amplitude in young cultures (Turrigiano et al. 1998;Wierenga et al. 2005) can also induce changes in mini frequency and in presynaptic release probability in older neuronal cultures (Wierenga et al. 2006), through a process that involves postsynaptic hyperpolarization and a drop in”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CELL-AUTONOMOUS, GLOBAL SYNAPTIC SCALING OF EXCITATORY SYNAPSES
What the sources say
- Not checked — no full text of the sourcecites Turrigiano et al. 1998 source
- Supportedcites Wierenga et al. 2005 source
Split into 2 atoms — 2 confirmed, 0 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
- Not checked — no full text of the sourcecites Wierenga et al. 2006 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
The sources with a verdict support this claim; the rest weren’t checked yet, have no full text we could read, or their verdicts aren’t rated yet.
In the paper
“Additionally, there is evidence that the neurotrophin brain-derived neurotrophic factor (BDNF) (Rutherford et al. 1998), the immediate early gene Arc (Shepherd et al. 2006), the cytokine TNFa (Stellwagen and Malenka 2006;Steinmetz and Turrigiano, 2010), the immune molecule MHC1 (Goddard et al. 2007), b3 integrins (Cingolani et al. 2008), the AMPAR binding protein PICK1 (Anggono et al. 2011), and”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CELL-AUTONOMOUS, GLOBAL SYNAPTIC SCALING OF EXCITATORY SYNAPSES
What the sources say
- Not checked — no full text of the sourcecites Rutherford et al. 1998 source
- Supportedcites Shepherd et al. 2006 source
The cited paper supports the Arc portion of the multi-citation claim. In “Arc/Arg3.1 Regulates Homeostatic Synaptic Scaling of AMPARs” (page unavailable), cultured wild-type hippocampal neurons showed activity-dependent changes in surface AMPA receptors, while Arc/Arg3.1 knockout neurons lacked those changes. The other molecules are attributed to other citations, not to this paper. (LLM, conf=0.94)
- Not matchedcites Stellwagen and Malenka 2006;Steinmetz and Turrigiano, 2010
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
Strength:plain· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Interestingly, chronic hyperpolarization of an entire neuron by expression of an inwardly rectifying K channel (K ir ) does not induce postsynaptic scaling (Burrone et al. 2002;Hou et al. 2008), suggesting that chronic global hyperpolarization of neuronal dendrites and somata overrides the signals that induce scaling up in response to a drop in firing.”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CELL-AUTONOMOUS, GLOBAL SYNAPTIC SCALING OF EXCITATORY SYNAPSES
What the sources say
- Not checked — no full text of the sourcecites Burrone et al. 2002 source
- Partly supportedcites Hou et al. 2008 sourceExperimental — accuracy not yet measured
Split into 2 atoms — 1 confirmed, 1 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“A number of reports have suggested that activity-dependent BDNF release is critical for scaling of inhibitory synapses onto pyramidal neurons as well as the homeostatic regulation of excitatory synapses onto inhibitory neurons (Rutherford et al. 1997(Rutherford et al. , 1998;;Copi et al. 2005;Swanwick et al. 2006).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > ROLE OF NETWORK ACTIVITY AND SECRETED FACTORS IN THE INDUCTION OF HOMEOSTATIC PLASTICITY
What the sources say
- Partly supportedcites Rutherford et al. 1997 sourceExperimental — accuracy not yet measured
The Discussion reports that activity blockade reduces inhibition onto cortical pyramidal neurons and that exogenous BDNF prevents this reduction, supporting the inhibitory part of the claim. It infers reduced endogenous BDNF production rather than directly demonstrating activity-dependent release, and it does not establish homeostatic regulation of excitatory synapses onto inhibitory neurons; the excitatory currents it mentions are onto pyramidal neurons. (LLM, conf=0.88)
- Not checked — no full text of the sourcecites Rutherford et al. 1998 source
- Not checked — no full text of the sourcecites Copi et al. 2005 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“TNFa signaling was not necessary for the induction of early (6 h) scaling, but became essential for maintenance of scaling during prolonged (.24 h) activity blockade.”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > ROLE OF NETWORK ACTIVITY AND SECRETED FACTORS IN THE INDUCTION OF HOMEOSTATIC PLASTICITY
What the sources say
- Supportedcites Steinmetz and Turrigiano 2010 source
The Results section reports that blocking TNFα signaling for 6 hours did not prevent early scaling, whereas 24 hours of blockade prevented scaling and reversed scaling that had already been induced. The Discussion interprets this as a requirement for TNFα signaling to maintain synapses’ ability to express or maintain scaling during prolonged activity blockade. (LLM, conf=0.92)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“This model is based on the observations that TNFa levels are elevated by prolonged (48 h) activity blockade, acute application of TNFa (or conditioned media from activity-blocked cultures) increases mEPSC amplitude, and scaling up in response to prolonged activity blockade is prevented by blocking TNFa signaling (Beattie et al. 2002;Stellwagen et al. 2005;Stellwagen and Malenka 2006).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > ROLE OF NETWORK ACTIVITY AND SECRETED FACTORS IN THE INDUCTION OF HOMEOSTATIC PLASTICITY
What the sources say
- Not checked — no full text of the sourcecites Beattie et al. 2002 source
- Partly supportedcites Stellwagen et al. 2005 sourceExperimental — accuracy not yet measured
The culture electrophysiology methods (page not provided) say TNFα was applied 15–25 minutes before recording, and the Figure 5 caption reports a significant increase in mEPSC amplitude in TNFα-treated cultures. The passages do not support the separate claim about conditioned media from activity-blocked cultures. (LLM, conf=0.85)
- Not checked — no full text of the sourcecites Stellwagen and Malenka 2006 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Synapses onto the same dendrite tended to have similar P r , and there was an inverse relationship between synapse number and P r onto individual dendrites, suggesting that this regulation happens in a”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > LOCAL AND QUASI-LOCAL FORMS OF HOMEOSTATIC SYNAPTIC PLASTICITY IN CENTRAL NEURONS
What the sources say
- Partly supportedcites Branco et al. 2008 sourceExperimental — accuracy not yet measured
Split into 2 atoms — 1 confirmed, 1 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“In apparent conflict with this model, a positive correlation between P r and synaptic strength at cortical synapses has been reported (Hardingham et al. 2010;Kay et al. 2011), but because in these studies synaptic strength was measured at unitary connections, it remains an open possibility that such an inverse correlation exists at the level of summed dendritic input.”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > LOCAL AND QUASI-LOCAL FORMS OF HOMEOSTATIC SYNAPTIC PLASTICITY IN CENTRAL NEURONS
What the sources say
- Supportedcites Hardingham et al. 2010 source
Split into 2 atoms — 2 confirmed, 0 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
- Could not verifycites Kay et al. 2011 sourceExperimental — accuracy not yet measured
Split into 2 atoms — 0 confirmed, 0 partially supported, 0 disputed, 0 misattributed, 2 unverifiable. Expand the claim to see per-atom verdicts.
Strength:hedged· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“This quasi-local (dendrite-wide) form of presynaptic homeostasis has been suggested to prevent synaptic saturation owing to strong depolarization from summed inputs onto a dendrite, by reducing P r when postsynaptic activation rises too high (Branco et al. 2008).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > LOCAL AND QUASI-LOCAL FORMS OF HOMEOSTATIC SYNAPTIC PLASTICITY IN CENTRAL NEURONS
What the sources say
- Supportedcites Branco et al. 2008 source
Split into 2 atoms — 2 confirmed, 0 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“BDNF was the first such secreted factor suggested to play a role in homeostatic plasticity (Rutherford et al. 1997(Rutherford et al. , 1998)).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > ROLE OF NETWORK ACTIVITY AND SECRETED FACTORS IN THE INDUCTION OF HOMEOSTATIC PLASTICITY
What the sources say
- Partly supportedcites Rutherford et al. 1997 sourceExperimental — accuracy not yet measured
The Discussion (page not specified in our copy) says BDNF regulates inhibition in cortical cultures and may help reduce inhibition when activity falls too low, supporting a role in homeostatic plasticity. The paper does not establish the historical claim that BDNF was the first secreted factor suggested to have that role. (LLM, conf=0.84)
- Not checked — no full text of the sourcecites Rutherford et al. 1998 source
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Unlike TTX treatment, acute TNFa application does not scale up mini amplitude and adding TNFa to prescaled synapses actually reduces synaptic strength, indicating that scaling and TNFa are neither additive nor simply occlusive (Steinmetz and Turrigiano 2010).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > ROLE OF NETWORK ACTIVITY AND SECRETED FACTORS IN THE INDUCTION OF HOMEOSTATIC PLASTICITY
What the sources say
- Supportedcites Steinmetz and Turrigiano 2010 source
The Results section, “Synaptic scaling modulates but does not occlude the effect of TNFα application,” reports that TNFα increased mEPSC amplitude at control synapses but did not produce the multiplicative change characteristic of TTX-induced scaling. Applied after 24 hours of TTX, it reduced mEPSC amplitude rather than adding to or merely occluding the increase. The supplied copy gives no page number for these passages. (LLM, conf=0.91)
Load-bearingStrength:hedged· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“In contrast, dark rearing increases the abundance of GluA2-lacking receptors and requires GluA1 phosphorylation, suggesting that these two modes of deprivation may induce different forms of compensatory synaptic plasticity (Goel and Lee 2007;Goel et al. 2011).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > FUNCTIONS OF HOMEOSTATIC PLASTICITY IN VIVO
What the sources say
- Partly supportedcites Goel and Lee 2007 sourceExperimental — accuracy not yet measured
The Results section (page unavailable) reports that two days of dark rearing increased AMPA receptor-mediated mEPSC amplitude in mouse visual cortex. The Discussion (page unavailable) says dark rearing increased GluR1 (GluA1) phosphorylation, but our copy does not establish that phosphorylation is required or that GluA2-lacking receptors become more abundant. (LLM, conf=0.83)
- Partly supportedcites Goel et al. 2011 sourceExperimental — accuracy not yet measured
The Results report that two days of dark exposure increased functional calcium-permeable AMPA receptors, consistent with more GluA2-lacking receptors; the Discussion says deprivation-induced synaptic changes require GluA1 phosphorylation. But the Methods specify that mice were raised under normal lighting until postnatal day 21, then exposed to darkness for two days. The paper does not establish these effects for dark rearing from birth. (LLM, conf=0.83)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Interestingly, binocularly driven neurons maintained a similar average level of combined responsiveness to the two eyes, suggesting that the drop in deprived eye responsiveness was compensated by an increase in nondeprived eye responsiveness (Mrsic-Flogel et al. 2007); a very similar response homeostasis following visual deprivation has been reported at retinotectal synapses (Chandrasekaran et al.”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > FUNCTIONS OF HOMEOSTATIC PLASTICITY IN VIVO
What the sources say
- Supportedcites Mrsic-Flogel et al. 2007 source
The paper states that neurons with binocular input adjusted their eye-specific responses so the summed visual response remained roughly preserved. It also reports that after monocular deprivation, deprived-eye responses fell while nondeprived-eye responses rose (Results, page unavailable). (LLM, conf=0.93)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“When one eye is deprived of patterned vision during the classical critical period (using lid suture) there is a change in the ability of the two eyes to drive neurons within the binocular portion of visual cortex: cortical neurons rapidly (within 2 or 3 days) lose responsiveness to the deprived eye, and then more slowly (over 4 -6 days) gain responsiveness to the nondeprived eye (Frenkel and Bear”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > FUNCTIONS OF HOMEOSTATIC PLASTICITY IN VIVO
What the sources say
- Not checked — no full text of the sourcecites Frenkel and Bear 2004 source
- Partly supportedcites Mrsic-Flogel et al. 2007 sourceExperimental — accuracy not yet measured
Split into 2 atoms — 1 confirmed, 1 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
- Not checked — no full text of the sourcecites Kaneko et al. 2008 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
Every source the paper cites for this claim was checked and supports it.
In the paper
“This possibility is raised by the finding that the same visual deprivation paradigm that scales minis up in younger mice produces nonmultiplicative changes in minis in older mice, suggesting that not all synapses are affected equally (Goel and Lee 2007); however, this could also reflect the simultaneous activation of synaptic scaling and Hebbian, synapse-specific mechanisms (see Turrigiano 2011”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > SPECIFICITY OF SYNAPTIC SCALING RULES FOR SYNAPSE TYPE
What the sources say
- Supportedcites Goel and Lee 2007 source
The “Loss of multiplicative synaptic scaling in adult mice” section reports that two days of dark rearing increased mEPSC amplitude multiplicatively in P23 mice (Fig. 4a). The same section reports that the increase in P97 mice did not follow a global multiplicative mechanism (Fig. 4e). (LLM, conf=0.94)
Strength:hedged· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Visual deprivation induced by optic nerve block scale ups mEPSC amplitude in vivo as in vitro, and results in insertion of GluA2-containing AMPAR (Desai et al. 2002;Maffei and Turrigiano 2008;Gainey et al. 2009).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > FUNCTIONS OF HOMEOSTATIC PLASTICITY IN VIVO
What the sources say
- Not checked — no full text of the sourcecites Desai et al. 2002 source
- Partly supportedcites Maffei and Turrigiano 2008 sourceExperimental — accuracy not yet measured
The Results section on experience-dependent plasticity at excitatory layer 2/3 synapses reports that visual deprivation by intraocular TTX injection increased AMPA mEPSC amplitude in rats. The paper does not establish an in vitro comparison or report insertion of GluA2-containing AMPARs, so those parts of the sentence are unsupported by this source. (LLM, conf=0.88)
- Supportedcites Gainey et al. 2009 source
The Results section reports that visual deprivation by intraocular TTX significantly increased mEPSC amplitude in visual cortical neurons. The Discussion states that scaling in vivo after monocular TTX injection increased accumulation of GluR2-containing AMPARs (now called GluA2-containing AMPARs), consistent with the claim. (LLM, conf=0.92)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“In visual cortex the expression of synaptic scaling is developmentally regulated (Desai et al. 2002;Maffei et al. 2004Maffei et al. , 2006;;Maffei and Turrigiano 2008); synaptic scaling is expressed by pyramidal neurons in layer 4 early in postnatal development, but then turns off in layer 4 and begins to be expressed in layer 2/3 pyramidal neurons around the opening of the classical visual system”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > SPECIFICITY OF SYNAPTIC SCALING RULES FOR SYNAPSE TYPE
What the sources say
- Not checked — no full text of the sourcecites Desai et al. 2002 source
- Supportedcites Maffei and Turrigiano 2008 source
Split into 2 atoms — 2 confirmed, 0 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
- Partly supportedcites Goel and Lee 2007 sourceExperimental — accuracy not yet measured
The Discussion (page unavailable) reports scaling in layer 4 at P14–P16 but not P21–P23, with the opposite pattern in layer 2/3; it also says the authors’ data extend layer 2/3 plasticity through adulthood. Our copy does not establish that the switch coincides with the opening of the classical visual critical period, or identify the early layer 4 cells specifically as pyramidal neurons. (LLM, conf=0.82)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“For example, reductions in glutamate receptor function, or chronic hyper-polarization of the muscle, lead to compensatory increases in transmitter release that restore evoked transmission to control levels (Paradis et al. 2001).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > HOMEOSTATIC PLASTICITY AT THE NEUROMUSCULAR JUNCTION
What the sources say
- Not checked — no full text of the sourcecites Paradis et al. 2001 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A claim is checked only against the cited paper’s full text, never its abstract, and none is available for its sources.
In the paper
“When cortical or hippocampal neurons are induced to fire more than normal, over many hours firing returns to baseline levels, and similarly, if neuronal firing is reduced over time, neurons compensate and again firing is restored (Fig. 1A) (Turrigiano et al. 1998;Burrone et al. 2002).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > HOMEOSTATIC PLASTICITY AT CENTRAL MAMMALIAN SYNAPSES
What the sources say
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Thus, without forces that prevent the excitability of the postsynaptic neuron from changing in response to correlation-based plasticity mechanisms, their specificity breaks down and information can no longer be effectively stored through differences in synaptic strengths.”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > Abstract
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“On a functional level, neuronal networks likely use this complex set of regulatory mechanisms to achieve homeostasis over a wide range of temporal and spatial scales.”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > Abstract
Tests✓ Asserted: passes✗ Checkable: fails✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim. It may be too vague to check against evidence.
In the paper
“More recently work at the mammalian and invertebrate NMJ has shown that perturbations in postsynaptic function can lead to compensatory changes in presynaptic release, and vice versa (Davis and Bezprozvanny 2001).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > HOMEOSTATIC PLASTICITY AT THE NEUROMUSCULAR JUNCTION
What the sources say
- Not checked — no full text of the sourcecites Davis and Bezprozvanny 2001 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Although all of these phenomena are theoretically capable of serving a homeostatic function, for many of them such a function has not been directly shown.”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > Abstract
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✗ Based: failsProbably not a substantial claim. The paper’s conclusions may not depend on it. The paper may give no reason why it holds.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Thus, cell-autonomously induced synaptic scaling is fundamentally different from LTP and LTD: it operates over a longer temporal scale (hours), a wider spatial scale (global), and utilizes distinct trafficking steps and molecular machinery to enhance or reduce the synaptic accumulation of GluA2-containing AMPAR at most if not all synapses onto a neuron.”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CELL-AUTONOMOUS, GLOBAL SYNAPTIC SCALING OF EXCITATORY SYNAPSES
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“The ability of synapses to undergo postsynaptic homeostatic regulation as a function of purely local changes in transmitter release and receptor activation thus remains controversial and may require either extreme presynaptic hyperpolarization (such as would be obtained with presynaptic expression of K ir ) or a situation in which spiking and transmitter release are both severely impaired (see”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > LOCAL AND QUASI-LOCAL FORMS OF HOMEOSTATIC SYNAPTIC PLASTICITY IN CENTRAL NEURONS
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“On the other hand, theoretical work has suggested that quasi-local forms of homeostasis that act on groups of nearby synapses can serve a useful normalization function without severely disrupting Hebbian plasticity (Rabinowitch and Segev 2006a,b).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > LOCAL AND QUASI-LOCAL FORMS OF HOMEOSTATIC SYNAPTIC PLASTICITY IN CENTRAL NEURONS
What the sources say
- Not matchedcites Rabinowitch and Segev 2006a,b
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
- Not matched
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“This suggests that a drop in somatic calcium influx will simultaneously enhance signaling in the pathways that scale synapses up and reduce signaling in the pathways that scale synapses down, and vice versa when firing rises.”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CELL-AUTONOMOUS, GLOBAL SYNAPTIC SCALING OF EXCITATORY SYNAPSES
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Such a postsynaptic scaling process has the attractive property of allowing neurons to stabilize activity without changing the relative strength of synaptic inputs, thus avoiding disrupting information storage or processing mechanisms that rely on differences in synaptic weights (Fig. 1B).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CELL-AUTONOMOUS, GLOBAL SYNAPTIC SCALING OF EXCITATORY SYNAPSES
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“The locus of change during homeostatic plasticity has important consequences for circuit function, because (for example) presynaptic changes in release probability will strongly affect short-term plasticity and thus the dynamics of information transfer across synapses, whereas a postsynaptic change in receptor accumulation can scale postsynaptic responsiveness without affecting the short-term”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CELL-AUTONOMOUS, GLOBAL SYNAPTIC SCALING OF EXCITATORY SYNAPSES
What the sources say
- Not checked — no full text of the sourcecites Abbott and Nelson 2000 source
Strength:boosted· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“Selectively blocking firing by microperfusion of TTX to the soma of individual neurons scales up synaptic strengths to the same degree as blockade of network activity, whereas local block of synaptic transmission does not induce a local enhancement of receptor accumulation (Ibata et al. 2008).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CELL-AUTONOMOUS, GLOBAL SYNAPTIC SCALING OF EXCITATORY SYNAPSES
What the sources say
- Not checked — no full text of the sourcecites Ibata et al. 2008 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“In dissociated cortical cultures it has been shown that excitatory synapses onto excitatory pyramidal neurons are scaled up by activity blockade, whereas excitatory synapses onto GA-BAergic interneurons are not (Rutherford et al. 1998).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > SPECIFICITY OF SYNAPTIC SCALING RULES FOR SYNAPSE TYPE
What the sources say
- Not checked — no full text of the sourcecites Rutherford et al. 1998 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“If this mechanism operates in vivo, it predicts an inverse relationship between P r and the summed synaptic strength onto a dendritic branch.”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > LOCAL AND QUASI-LOCAL FORMS OF HOMEOSTATIC SYNAPTIC PLASTICITY IN CENTRAL NEURONS
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim.
In the paper
“This is consistent with evidence that chronic hyperpolarization of entire neurons (including dendrites) results in enhanced P r (Burrone et al. 2002), suggesting that P r can be bidirectionally regulated by changes in the amount of dendritic depolarization.”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > LOCAL AND QUASI-LOCAL FORMS OF HOMEOSTATIC SYNAPTIC PLASTICITY IN CENTRAL NEURONS
What the sources say
- Not checked — no full text of the sourcecites Burrone et al. 2002 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Blocking BDNF signaling mimics, and exogenous BDNF application prevents, the effects of activity blockade on excitatory minis, suggesting that in neocortical neurons activitydependent BDNF release could mediate synaptic scaling (Rutherford et al. 1998).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > ROLE OF NETWORK ACTIVITY AND SECRETED FACTORS IN THE INDUCTION OF HOMEOSTATIC PLASTICITY
What the sources say
- Not checked — no full text of the sourcecites Rutherford et al. 1998 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“BDNF is thought to be released as a function of pyramidal neuron activity, and activates Trk receptors on both pyramidal and interneurons (Lu 2003).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > ROLE OF NETWORK ACTIVITY AND SECRETED FACTORS IN THE INDUCTION OF HOMEOSTATIC PLASTICITY
What the sources say
- Not matchedcites Lu 2003
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Not matched
In the paper
“It was recently proposed that prolonged activity blockade (with TTX) increases glial release of TNFa, which then acts on neurons to enhance AMPAR insertion and scale up mEPSC amplitude (Stellwagen and Malenka 2006).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > ROLE OF NETWORK ACTIVITY AND SECRETED FACTORS IN THE INDUCTION OF HOMEOSTATIC PLASTICITY
What the sources say
- Not checked — no full text of the sourcecites Stellwagen and Malenka 2006 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“These distinct plasticity rules at different classes of excitatory and inhibitory synapse are consistent with an overall homeostatic shift in the balance between excitation and inhibition, as the net effect of the changes induced by activity blockade are to enhance excitation and reduce inhibition, which will act to restore network excitability.”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > SPECIFICITY OF SYNAPTIC SCALING RULES FOR SYNAPSE TYPE
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Interestingly, not all excitatory neurons in cortical networks express synaptic scaling.In hippocampal networks CA1 neurons scale synapses up in response to activity blockade, whereas CA3 neurons do not (Kim and Tsien 2008).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > SPECIFICITY OF SYNAPTIC SCALING RULES FOR SYNAPSE TYPE
What the sources say
- Not checked — no full text of the sourcecites Kim and Tsien 2008 source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
A claim is checked only against the cited paper’s full text, never its abstract, and none is available for its sources.
In the paper
“Interestingly, in visual cortical microcircuits the locus of homeostatic plasticity changes as the circuit matures.Early in postnatal development layer 4 (the first input layer to cortex, and the first layer to mature) responds homeostatically to brief (2 days) inactivation of the optic nerve with TTX (Desai et al. 2002;Maffei et al. 2004), whereas later (at the opening of the classical visual”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > FUNCTIONS OF HOMEOSTATIC PLASTICITY IN VIVO
What the sources say
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“When sensory drive to primary visual cortex is lowered in vivo, connections from fast-spiking basket cells onto layer 4 pyramidal neurons are reduced in amplitude, whereas connections from another class of interneuron become sparser but stronger (Maffei et al. 2004).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > SPECIFICITY OF SYNAPTIC SCALING RULES FOR SYNAPSE TYPE
What the sources say
- Not checked — no full text of the sourcecites Maffei et al. 2004 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Similarly, in visual cortex during the second and third postnatal weeks when synaptogenesis is high, there is an inverse relationship between the frequency and amplitude of mEPSCs onto pyramidal neurons, and this can be prevented by raising animals in the dark (Desai et al. 2002).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > FUNCTIONS OF HOMEOSTATIC PLASTICITY IN VIVO
What the sources say
- Not checked — no full text of the sourcecites Desai et al. 2002 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Neurons and networks use a family of homeostatic synaptic plasticity mechanisms to stabilize firing rates in the face of developmental or learning-induced changes in drive, and this contributes to the ability of central neuronal networks to maintain stable function and enables networks to maintain the specificity of synaptic changes that encode information.”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CONCLUDING REMARKS
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
The paper relies on this without support.
Neural circuits must maintain stable function in the face of plastic challenges including changes in synapse number and strength during learning and development.
“Neural circuits must maintain stable function in the face of many plastic challenges, including changes in synapse number and strength, during learning and development.”
The paper relies on this without support.
At the neuromuscular junction, as muscle fibers grow, motor neurons must remain capable of bringing them over threshold for contraction.
“The stability problem at the neuromuscular junction (NMJ) is fairly simple: As muscle fibers grow, motor neurons must remain capable of bringing them over threshold for contraction.”
The paper relies on this without support.
The forces that generate flexibility and those that generate stability are able to coexist without interfering with each other.
“Somehow the forces that generate flexi-bility and those that generate stability are able to coexist without interfering with each other, and together enable the remarkable ability of organisms to generate behaviors that are both coherent and adaptable.”
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The check wasn’t confident either way, so it gives no verdict — never disputed.
In the citing paper
“normalizing by the total number of incoming synapses provides a form of homeostatic synaptic scaling46.”
From Predicting modular functions and neural coding of behavior from a synaptic wiring diagram (2024) · cites this paper as [46]
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
Each contradiction between two passages listed here was confirmed by an independent check.
Evers study has conflicting publication years
MinorThe text cites the Evers study as published in 2011, but the corresponding reference lists it as published in 2010.
“(Evers et al. 2011)”
“29. Evers DM, Matta JA, Hoe HS, Zarkowsky D, Lee SH, Isaac JT, Pak DT. 2010. Plk2 attachment to NSF induces homeo- static removal of GluA2 during chronic overexcitation.”
Citations
Cites
Malenka, R. C., & Bear, M. F. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.012 · Cited by 3,968
Bienenstock, E., Cooper, L., & Munro, P. (1982) · The Journal of Neuroscience · doi:10.1523/jneurosci.02-01-00032.1982 · Cited by 2,896
Homeostatic plasticity in the developing nervous system
Turrigiano, G. G., & Nelson, S. B. (2004) · Nature Reviews Neuroscience · doi:10.1038/nrn1327 · Cited by 2,485
Self-citationSynaptic plasticity: taming the beast
Abbott, L. F., & Nelson, S. B. (2000) · Nature Neuroscience · doi:10.1038/81453 · Cited by 2,263 · cited 1×
“The online first http://cshperspectives.cshlp.org/site/misc/subscribe.xhtml go to: Cold Spring Harbor Perspectives in BiologyTo subscribe to Copyright © 2011 Cold Spring Harbor Laboratory Press; all rights reserved”
MethodActivity-dependent scaling of quantal amplitude in neocortical neurons
Turrigiano, G. G., Leslie, K. R., Desai, N. S., Rutherford, L. C., & Nelson, S. B. (1998) · Nature · doi:10.1038/36103 · Cited by 2,226
Self-citationSynaptic scaling mediated by glial TNF-α
Stellwagen, D., & Malenka, R. C. (2006) · Nature · doi:10.1038/nature04671 · Cited by 1,715
The self-tuning neuron: synaptic scaling of excitatory synapses
Turrigiano, G. G. (2008) · Cell · doi:10.1016/j.cell.2008.10.008 · Cited by 1,533
Self-citationControl of Synaptic Strength by Glial TNFα
Beattie, E. C., Stellwagen, D., Morishita, W., Bresnahan, J. C., Ha, B. K., Von Zastrow, M., Beattie, M. S., & Malenka, R. C. (2002) · Science · doi:10.1126/science.1067859 · Cited by 1,344
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Variability, compensation and homeostasis in neuron and network function
Marder, E., & Goaillard, J.-M. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn1949 · Cited by 1,212
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Kawata, S., Miyazaki, T., Yamazaki, M., Mikuni, T., Yamasaki, M., Hashimoto, K., Watanabe, M., Sakimura, K., & Kano, M. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.07.014 · Cited by 25
Gruenbaum, B. F., Schonwald, A., Boyko, M., & Zlotnik, A. A. (2024) · Cells · doi:10.3390/cells13141228 · Cited by 26
“Under physiological circumstances, neurons uphold a certain threshold that ensures synaptic homeostasis, as seen in long-term potentiation [20,41].”
BackgroundRoles and Transcriptional Responses of Inhibitory Neurons in Learning and Memory
Giorgi, C., & Marinelli, S. (2021) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2021.689952 · Cited by 24
Neurofeedback and neural self-regulation: a new perspective based on allostasis
Mirifar, A., Keil, A., & Ehrlenspiel, F. (2022) · Reviews in the Neurosciences · doi:10.1515/revneuro-2021-0133 · Cited by 30
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“…a prime example of this phenomenon (Turrigiano et al., 1998; Turrigiano, 1999; Desai 7 et al., 2002; Turrigiano and Nelson, 2004; Wallace and Bear, 2004; Wierenga et al., 2005; Maffei and 8 Turrigiano, 2008; Turrigiano, 2012; Keck et al., 2013; Nahmani and Turrigiano, 2014, Nys et al., 2015).”
Robust cone-mediated signaling persists late into rod photoreceptor degeneration
Scalabrino, M. L., Thapa, M., Chew, L. A., Zhang, E., Xu, J., Sampath, A. P., Chen, J., & Field, G. D. (2022) · eLife · doi:10.7554/elife.80271 · Cited by 27
“…with RP45 (Cngb1 mutations) maintain cone vision for many years, but the assumption has been that vision was preserved primarily through cortical compensation (Ferreira et al., 2017; Hickmott & Merzenich, 2002; Keck et al., 2013, 2008, 2011; Merabet & Pascual-Leone, 2010; Turrigiano, 2012).”
BackgroundAstrocyte and Neuronal Plasticity in the Somatosensory System
Sims, R. E., Butcher, J. B., Parri, H. R., & Glazewski, S. (2015) · Neural Plasticity · doi:10.1155/2015/732014 · Cited by 28
“This form of plasticity limits excitatory drive and thereby prevents eventual excitotoxic damage during addition of excitatory connections during development [21–23].”
BackgroundBecker, D., Ikenberg, B. D., Schiener, S., Maggio, N., & Vlachos, A. (2014) · Neuropharmacology · doi:10.1016/j.neuropharm.2014.07.013 · Cited by 24
The Synaptic Scaling Literature: A Systematic Review of Methodologies and Quality of Reporting
Moulin, T. C., Rayêe, D., Williams, M. J., & Schiöth, H. B. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00164 · Cited by 26
“That is a somewhat counterintuitive preference, as the field has long stated the theoretical importance of homeostatic mechanisms for protecting network stability, usually from the effects of excessive activity caused by Hebbian types of plasticity (Abbott and Nelson, 2000; Turrigiano, 2012).”
BackgroundRen, L. (2024) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2023.110910 · Cited by 23
“Homeostatic self-tuning processes that maintain the balance of excitation and inhibition (E/I) and the average firing rates of neurons are crucial to the stable functioning of neuronal networks in the face of abrupt fluctuations in neural excitability (Turrigiano, 2012).”
BackgroundBlackwell, K. T., Salinas, A. G., Tewatia, P., English, B. W., Kotaleski, J. H., & Lovinger, D. M. (2018) · European Journal of Neuroscience · doi:10.1111/ejn.13919 · Cited by 21
“that TBS LTP is accompanied by heterosynaptic LTD, and suggests a mechanism underlying homeostatic scaling (Turrigiano, 2012).”
BackgroundHomeostatic coordination and up-regulation of neural activity by activity-dependent myelination
Talidou, A., Frankland, P. W., Mabbott, D., & Lefebvre, J. (2022) · Nature Computational Science · doi:10.1038/s43588-022-00315-z · Cited by 29
Neuroplastic changes in the sensorimotor cortex associated with orthodontic tooth movement in rats
Sood, M., Lee, J., Avivi‐Arber, L., Bhatt, P., & Sessle, B. J. (2015) · The Journal of Comparative Neurology · doi:10.1002/cne.23753 · Cited by 23
Gonzalez-Islas, C. E., García-Bereguiain, M. Á., & Wenner, P. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.1229-12.2012 · Cited by 23
“Increasing SNA through chronic blockade of endocannabinoid signaling reduces AMPA and GABA mPSC amplitude Synaptic scaling is a form of homeostatic plasticity that increases or decreases the strength of all synapses onto a neuron by a scaling factor to stabilize firing rates (Turrigiano, 2012).”
BackgroundMoreau, A. W., Amar, M., Callebert, J., & Fossier, P. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.02.013 · Cited by 25
“Such changes in the maturation of cortical circuits could in turn modify the crosstalk between excitatory and inhibitory neurons that normally occurs during homeostatic plasticity (Le Roux et al., 2006; Maffei and Turrigiano, 2008; Turrigiano, 2012).”
BackgroundNonreciprocal homeostatic compensation in Drosophila potassium channel mutants
Kim, E. Z., Vienne, J., Rosbash, M., & Griffith, L. C. (2017) · Journal of Neurophysiology · doi:10.1152/jn.00002.2017 · Cited by 25
“Remarkable homeostatic compensations that protect against potentially debilitating electrical activity have been observed in vertebrates (Turrigiano 2012) and in electrophysiologically accessible invertebrate systems, such as the crustacean stomatogastric ganglion (Marder and Bucher 2007), the Drosophila neuromuscular…”
BackgroundFink, J. J., & Levine, E. S. (2018) · Frontiers in Neurology · doi:10.3389/fneur.2018.00237 · Cited by 26
Klos, C., Miner, D. C., & Triesch, J. (2018) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1006187 · Cited by 22
Shimizu, T., Hanajima, R., Shirota, Y., Tsutsumi, R., Tanaka, N., Terao, Y., Hamada, M., & Ugawa, Y. (2019) · Brain stimulation · doi:10.1016/j.brs.2019.08.001 · Cited by 25
“Homeostatic plasticity is the homeostatic regulation of synaptic plasticity inwhich the capacity of synapses to exhibit plasticity depends on prior levels of neuronal activity [53,54].”
Single Synapse LTP: A Matter of Context?
Kruijssen, D. L. H., & Wierenga, C. J. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00496 · Cited by 26
“Homeostatic plasticity operates over long time scales to maintain neuronal network function (Turrigiano, 2012).”
BackgroundSahin, G. S., Dhar, M., Dillon, C., Zhu, M., Shiina, H., Winters, B. D., Lambert, T. J., Impey, S., Appleyard, S. M., & Wayman, G. A. (2020) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2020.103500 · Cited by 24
“Interestingly, caSTAT3 did not further decrease the basal spine density, suggesting that either already existing pSTAT3 levels did not change significantly or how much active STAT3 can block normal development of spines is tightly regulated due to homeostatic synaptic plasticity (Turrigiano, 2012).”
BackgroundRescue of Inhibitory Synapse Strength following Developmental Hearing Loss
Kotak, V. C., Takesian, A. E., MacKenzie, P. C., & Sanes, D. H. (2013) · PLoS ONE · doi:10.1371/journal.pone.0053438 · Cited by 23
Responses of Cortical Neurons to Intracortical Microstimulation in Awake Primates
Yun, R., Mishler, J. H., Perlmutter, S. I., Rao, R. P. N., & Fetz, E. E. (2023) · eNeuro · doi:10.1523/eneuro.0336-22.2023 · Cited by 25
“Although the examined network size, location, and synaptic connections vary greatly, the strong consensus is that excitation and inhibition are generally comodulated (Chen, 2004; Haider, 2006; Isaacson and Scanziani, 2011; Turrigiano, 2012; Xue et al., 2014; Rubin et al., 2017).”
Kasai, H. (2023) · Proceedings of the Japan Academy Series B · doi:10.2183/pjab.99.018 · Cited by 25
Synapse-specific structural plasticity that protects and refines local circuits during LTP and LTD
Harris, K. M., Kuwajima, M., Flores, J. C., & Zito, K. (2024) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2023.0224 · Cited by 22
Huang, Z., Tong, C., Zhao, Y., Jiang, L., Deng, L., Gao, X., He, J., & Jiang, J. (2024) · Nanoscale · doi:10.1039/d4nr02350a · Cited by 22
Song, Y., Zhang, J., & Chen, C. (2015) · Scientific Reports · doi:10.1038/srep16257 · Cited by 23
Nozari, E., & Cortés, J. (2020) · IEEE Transactions on Automatic Control · doi:10.1109/tac.2020.3004801 · Cited by 23
“Interestingly, several works in the neuroscience literature have shown that neuronal networks maintain stability by re-scaling their synaptic weights that change during learning, a process commonly referred to as homeostatic synaptic plasticity [71].”
BackgroundLezmy, J., Gelman, H., Katsenelson, M., Styr, B., Tikochinsky, E., Lipinsky, M., Peretz, A. S., Slutsky, I., & Attali, B. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.1914-19.2020 · Cited by 24
“The homeostatic regulation of intrinsic excitability involves alterations in ion channels expression and in the structural organization of the axon initial segment (AIS; Turrigiano, 2011, 2012; Yoshimura and Rasband, 2014; Kole and Brette, 2018).”
BackgroundInfluentialPatel, P. A., Liang, C., Arora, A., Vijayan, S., Ahuja, S., Wagley, P. K., Settlage, R. E., LaConte, L. E. W., Goodkin, H. P., Lazar, I. M., et al. (2020) · Experimental Neurology · doi:10.1016/j.expneurol.2020.113319 · Cited by 23
“synaptic scaling, utilizing mechanisms independent of those traditionally associated with long-term potentiation/depression [76,77].”
Changes in Striatal Medium Spiny Neuron Morphology Resulting from Dopamine Depletion Are Reversible
Witzig, V. S., Komnig, D., & Falkenburger, B. H. (2020) · Cells · doi:10.3390/cells9112441 · Cited by 27
“Homeostatic plasticity allows neuronal networks to maintain a stable rate of activity when synapses change [5].”
BackgroundShort-term plasticity in the human visual thalamus
Kurzawski, J. W., Lunghi, C., Biagi, L., Tosetti, M., Morrone, M. C., & Binda, P. (2022) · eLife · doi:10.7554/elife.74565 · Cited by 27
“…Lunghi et al., 2013; Lunghi et al., 2015b; Lunghi and Sale, 2015c; Lunghi et al., 2019; Lyu et al., 2020; Min et al., 2018; Schwenk et al., 2020; Wang et al., 2020; Zhou et al., 2015; Zhou et al., 2013; Zhou et al., 2014) that was interpreted as a form of homeostatic plasticity (Turrigiano, 2012).”
BackgroundDendritic plateau potentials can process spike sequences across multiple time-scales
Leugering, J., Nieters, P., & Pipa, G. (2023) · Frontiers in Cognition · doi:10.3389/fcogn.2023.1044216 · Cited by 24
“The localized coincidence detection requires homeostatic processes to adjust synaptic transmission probabilities (Turrigiano, 2012; Leugering and Pipa, 2018) in order to appropriately balance the excitability threshold and synaptic input.”
BackgroundGhosh, R., Vegesna, S., Safi, R., Bao, H., Zhang, B., Marenda, D. R., & Liebl, F. L. W. (2014) · PLoS ONE · doi:10.1371/journal.pone.0113494 · Cited by 22
Patel, V., Oh, A. Y., Voit, A., Sultatos, L., Babu, G. J., Wilson, B., Ho, M., & Mcardle, J. (2014) · PLoS ONE · doi:10.1371/journal.pone.0110571 · Cited by 19
“The process of synaptic homeostasis [39, 40], via retrograde signaling, enables motor nerves to compensate for post-synaptic receptor loss [41] or endplate AChR loss during AChR-MG [42] by increasing neurotransmitter release.”
BackgroundJeanneret, V., & Yepes, M. (2016) · Translational Stroke Research · doi:10.1007/s12975-016-0454-x · Cited by 22
“Although the induction of LTP plays an important role in physiological processes such as learning and memory formation [83, 84] and in recovery of neurological function after an”
Steinmetz, C. C., Tatavarty, V., Sugino, K., Shima, Y., Joseph, A., Lin, H. K., Rutlin, M. L., Lambo, M. E., Hempel, C. M., Okaty, B. W., et al. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.08.009 · Cited by 22
Self-citationCeglia, I., Lee, K.-W., Cahill, M. E., Graves, S. M., Dietz, D., Surmeier, D. J., Nestler, E. J., Nairn, A. C., Greengard, P., & Kim, Y. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1621185114 · Cited by 21
“The WAVE1-regulated decrease of glutamatergic synapses on D1-MSNs in NAc in response to cocaine challenge following withdrawal might be part of a homeostatic feedback mechanism to avoid excessive increases in excitatory input and to thereby maintain network stability (61, 62).”
BackgroundGiacco, V., Panattoni, G., Medelin, M., Bonechi, E., Aldinucci, A., Ballerini, C., & Ballerini, L. (2019) · Journal of Neuroinflammation · doi:10.1186/s12974-019-1519-z · Cited by 22
“, post-synaptic currents, might be misleading, due to the variable amount of homeostatic plasticity taking place once destabilizing influences alter synaptic transmission [56].”
Neural Circuit Reprogramming: A New Paradigm for Treating Neuropsychiatric Disease?
Tye, K. M. (2014) · Neuron · doi:10.1016/j.neuron.2014.08.022 · Cited by 21
“Homeostatic plasticity mechanisms are generally conceptualized to serve as a stabilizing force in a highly plastic system to keep synapses within a functional dynamic range and prevent the overexcitation (or inhibition) that could occur with Hebbian plasticity mechanisms (Turrigiano, 2012).”
BackgroundSpecificity protein 4 (Sp4) transcriptionally regulates inhibitory GABAergic receptors in neurons
Nair, B. J., Johar, K., Priya, A., & Wong‐Riley, M. T. T. (2015) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2015.10.005 · Cited by 21
Braegelmann, K. M., Streeter, K., Fields, D. P., & Baker, T. L. (2016) · Experimental Neurology · doi:10.1016/j.expneurol.2016.07.012 · Cited by 21
“As neuronal information flow tends to converge on AMPA receptor activation (Turrigiano, 2012), many of the molecules identified in homeostatic plasticity are known to regulate AMPA receptor trafficking, such as stargazin (Louros et al.”
InfluentialMoulin, T. C., Petiz, L. L., Rayêe, D., Winne, J., Maia, R. G., da Cruz, R. V. L., Amaral, O. B., & Leão, R. N. (2019) · Hippocampus · doi:10.1002/hipo.23080 · Cited by 21
“As a counterpart to input-specific Hebbian plasticity, thus, neurons can sense changes in their excitability and initiate global homeostatic regulations in synapses to restrain their activity to its usual physiological range, in a process known as synaptic scaling (Turrigiano, 2012).”
BackgroundHuang, W., Ke, Y., Zhu, J., Liu, S., Cong, J., Ye, H., Guo, Y., Wang, K., Zhang, Z., Meng, W., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109404 · Cited by 22
Rutherford, M. A., Bhattacharyya, A., Xiao, M., Cai, H.-M., Pal, I., & Rubio, M. E. (2023) · eLife · doi:10.7554/elife.80950 · Cited by 21
“In the context of homeostatic synaptic plasticity (Turrigiano, 2012), an increase in synaptic current size due to increased proportion of CP- AMPARs could be compensated by net removal of AMPARs.”
BackgroundEpigenetic Regulation of SNAP25 Prevents Progressive Glutamate Excitotoxicty in Hypoxic CA3 Neurons
Biswal, S., Das, D., Barhwal, K. K., Kumar, A., Nag, T. C., Thakur, M. K., Hota, S. K., & Kumar, B. (2016) · Molecular Neurobiology · doi:10.1007/s12035-016-0156-0 · Cited by 21
“While, activity-dependent synaptic plasticity is normally associated with glutamatemediated strengthening of active synapses and increased post-synaptic density [32, 33], we observed an interesting phenomenon of synaptic weakening due to increased synaptic activity as a result of excitotoxic glutamate release during c…”
BackgroundLamina-specific AMPA receptor dynamics following visual deprivation in vivo
Tan, H. L., Roth, R. H., Graves, A. R., Cudmore, R. H., & Huganir, R. L. (2020) · eLife · doi:10.7554/elife.52420 · Cited by 20
“…and this has been extensively characterized in vitro and ex vivo (Desai et al., 2002; Goel et al., 2006; Goel and Lee, 2007; O’Brien et al., 1998; Turrigiano, 2012; Turrigiano et al., 1998), where chronic visual deprivation induces up-regulation of synaptic AMPARs in the primary visual cortex…”
BackgroundInfluentialSignaling in the Brain: In Search of Functional Units
Cao, R. (2014) · Philosophy of Science · doi:10.1086/677688 · Cited by 25
“…Hebbian and anti-Hebbian mechanisms, which change synaptic strength depending on whether the synapse receives input that is coordinated in the right way (or wrong way) with its neighbors on the same cell, there are a variety of other kinds of locally regulated synaptic plasticity (Turrigiano 2012).”
BackgroundMattioni, S., Rezk, M., Battal, C., Vadlamudi, J., & Collignon, O. (2022) · eLife · doi:10.7554/elife.79370 · Cited by 25
“41 to the homeostatic plasticity mechanisms, extensively described at the synaptic level (Keck et al., 2017; Turrigiano, 2012; Whitt, Petrus, & Lee, 2013).”
BackgroundAgüi‐Gonzalez, P., Bao, G., de Castro, M. A. G., Rizzoli, S. O., & Phan, N. T. N. (2021) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.1c00031 · Cited by 20
Jiang, Y., & VanDongen, A. M. J. (2021) · eNeuro · doi:10.1523/eneuro.0540-20.2021 · Cited by 19
“It has long been thought that plasticity mechanisms cause networks to destabilize (Abbott and Nelson, 2000), and many cellular and network mechanisms, generally termed as homeostatic plasticity, have been discovered to push their state back to baseline (Turrigiano, 2012).”
BackgroundInfluences of Glaucoma on the Structure and Function of Synapses in the Visual System
Hook, M. J. V. (2022) · Antioxidants and Redox Signaling · doi:10.1089/ars.2021.0253 · Cited by 21
“In homeostatic plasticity, neurons attempt to maintain a stable firing rate in response to altered network activity by altering synaptic responsiveness or intrinsic excitability (110, 159).”
Krentzel, A. A., Proaño, S. B., Dorris, D. M., Setzer, B., & Meitzen, J. (2022) · Journal of Neuroendocrinology · doi:10.1111/jne.13122 · Cited by 19
“changes in excitatory synaptic input and intrinsic excitability compensate for each other to mitigate differential circuit output, perhaps via an estrous cycle associated homeostatic plasticity mechanism, as detailed in other circumstances.(119,120) This second interpretation is based upon potentially compensatory cha…”
MethodenrichMiR predicts functionally relevant microRNAs based on target collections
Soutschek, M., Germade, T., Germain, P., & Schratt, G. M. (2022) · Nucleic Acids Research · doi:10.1093/nar/gkac395 · Cited by 20
Dentate gyrus is needed for memory retrieval
Carretero‐Guillén, A., Treviño, M., Gómez‐Climent, M. Á., Dogbevia, G., Bertocchi, I., Sprengel, R., Larkum, M. E., Vlachos, A., Gruart, A., Delgado-Garcia, J. M., et al. (2024) · Molecular Psychiatry · doi:10.1038/s41380-024-02546-0 · Cited by 22
“Inhibition of neuronal activity by hyperpolarization can interfere with numerous biochemical processes [42] that, in turn, could disrupt intrinsic [50], synaptic [38], and homeostatic plasticity [51], and thus learning and memory processes.”
BackgroundKusek, M., Tokarski, K., & Hess, G. (2013) · PubMed · Cited by 20
MSK1 regulates transcriptional induction of Arc/Arg3.1 in response to neurotrophins
Hunter, C. J., Reményi, J., Corrêa, S. A. L., Privitera, L., Reyskens, K. M. S. E., Martin, K. J., Toth, R. L., Frenguelli, B. G., & Arthur, J. S. C. (2017) · FEBS Open Bio · doi:10.1002/2211-5463.12232 · Cited by 20
Keppler, H., Degeest, S., & Dhooge, I. J. M. (2017) · The Journal of Laryngology & Otology · doi:10.1017/s0022215117001803 · Cited by 20
Lo, F., & Erzurumlu, R. S. (2018) · Molecular Autism · doi:10.1186/s13229-018-0196-6 · Cited by 20
Cul4 ubiquitin ligase cofactor DCAF12 promotes neurotransmitter release and homeostatic plasticity
Patrón, L. A., Nagatomo, K., Eves, D. T., Imad, M., Young, K., Torvund, M., Guo, X., Rogers, G. C., & Zinsmaier, K. E. (2019) · The Journal of Cell Biology · doi:10.1083/jcb.201805099 · Cited by 21
“…plasticity maintains normal postsynaptic excitation in response to a decrease in postsynaptic neurotransmitter receptor sensitivity and requires transsynaptic signaling to up-regulate evoked release (Petersen et al., 1997; DiAntonio et al., 1999; Davis, 2006; Turrigiano, 2012; Frank, 2014).”
BackgroundPharmacological and Pathological Implications of Sigma-1 Receptor in Neurodegenerative Diseases
Drewes, N. B., Fang, X., Gupta, N., & Nie, D. (2025) · Biomedicines · doi:10.3390/biomedicines13061409 · Cited by 22
“All of these mechanisms support the maintenance of homeostatic plasticity, a process critical to the stabilization of neural pathways, and are central to preventing neurodegeneration [102,103].”
A feedback control principle common to several biological and engineered systems
Suen, J. Y., & Navlakha, S. (2022) · Journal of The Royal Society Interface · doi:10.1098/rsif.2021.0711 · Cited by 23
“In the brain, homeostatic plasticity mechanisms [49] are used to stabilize network activity to remain in preferred ranges [50].”
BackgroundMechanisms Driving the Emergence of Neuronal Hyperexcitability in Fragile X Syndrome
Bülow, P., Segal, M., & Bassell, G. J. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23116315 · Cited by 22
“Homeostatic plasticity ensures that neuronal activity levels are kept within a physiologically appropriate range certifying that synaptic strength or intrinsic excitability does not saturate and impair Hebbian plasticity [98,99].”
BackgroundInfluentialMcGregor, J. N., Farris, C. A., Ensley, S., Schneider, A. M., Fosque, L. J., Wang, C., Tilden, E. I., Liu, Y., Tu, J., Elmore, H., et al. (2024) · Neuron · doi:10.1016/j.neuron.2024.08.006 · Cited by 23
“2,3 6 However, there are perturbations for which the brain is unable to compensate—principal among these is neurodegenerative disease (NDD), which progressively undermines brain function.”
BackgroundRegulation of PV interneuron plasticity by neuropeptide-encoding genes
Selten, M. M., Bernard, C., Mukherjee, D., Hamid, F., Hanusz-Godoy, A., Oozeer, F., Zimmer, C., & Marín, Ó. (2025) · Nature · doi:10.1038/s41586-025-08933-z · Cited by 19
Neuropeptide orphanin FQ inhibits dendritic morphogenesis through activation of RhoA
Alder, J., Kallman, S., Palmieri, A. J., Khadim, F., Ayer, J., Kumar, S., Tsung, K., Grinberg, I., & Thakker‐Varia, S. (2013) · Developmental Neurobiology · doi:10.1002/dneu.22101 · Cited by 20
“Synaptic homeostasis results from a fine balance of stimulatory and inhibitory mechanisms that allow neurons to maintain stable function during periods of perturbation such as developmental and activitydependent alterations in synapse number or strength (Turrigiano, 2012).”
BackgroundDietrich, H., & Straka, H. (2016) · European Journal of Neuroscience · doi:10.1111/ejn.13269 · Cited by 19
“…elevated or diminished cellular/network activity and © 2016 Federation of European Neuroscience Societies and John Wiley & Sons Ltd European Journal of Neuroscience, 44, 1787–1796 to maintain stability of the neuronal encoding as previously described in other brain areas (Turrigiano, 2012).”
BackgroundLSD1 is an environmental stress-sensitive negative modulator of the glutamatergic synapse
Longaretti, A., Forastieri, C., Toffolo, E., Caffino, L., Locarno, A., Misevičiūtė, I., Marchesi, E., Battistin, M., Ponzoni, L., Madaschi, L., et al. (2020) · Neurobiology of Stress · doi:10.1016/j.ynstr.2020.100280 · Cited by 20
“physiologically engage neuroLSD1 downregulation), we obtained the same effect on mEPSCs that can be obtained by eliciting homeostatic synaptic plasticity via sustained glutamate stimulation (Xu and Pozzo-Miller, 2017; Turrigiano, 2012).”
BackgroundBachmann, C., Tetzlaff, T., Duarte, R., & Morrison, A. (2020) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1007790 · Cited by 19
“Such a homeostatic stabilization of the population firing rate can be accounted for by a global adjustment of synaptic weights (synaptic scaling; Vitureira et al., 2012; Turrigiano, 2012).”
Homeostatic synaptic plasticity rescues neural coding reliability
Rozenfeld, E., Ehmann, N., Manoim, J. E., Kittel, R. J., & Parnas, M. (2023) · Nature Communications · doi:10.1038/s41467-023-38575-6 · Cited by 19
“Homeostatic synaptic plasticity describes a phenomenon whereby pre-or postsynaptic adjustments maintain synaptic stability 7 – 10 .”
Koesters, A. G., Rich, M. M., & Engisch, K. L. (2024) · The Neuroscientist · doi:10.1177/10738584221112336 · Cited by 17
“These stated that there are global and local homeostatic mechanisms (Chen and others 2012; Fernandes and Carvalho 2016; Lee 2012; Turrigiano 2008, 2011, 2012, 2017; Vitureira and Goda 2013; Yu and Goda 2009); that uniform multiplicative homeostatic plasticity may sometimes be obscured by other…”
BackgroundInfluentialDecoding halide perovskites for neuromorphic and memristive devices
Das, D., Assi, D. S., Kazim, S., Roy, V. A. L., & Ahmad, S. (2025) · Materials Horizons · doi:10.1039/d5mh00534e · Cited by 18
Presynaptic inhibition rapidly stabilises recurrent excitation in the face of plasticity
Naumann, L., & Sprekeler, H. (2020) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1008118 · Cited by 19
“Second, synaptic scaling operates on the spatial scale of single neurons [44], thus affecting the relative contribution of different neurons to network activity— albeit differently from short-term depression in that input and not output synapses are modulated.”
BackgroundMolecular Mechanisms of Memory Consolidation That Operate During Sleep
Reyes‐Resina, I., Samer, S., Kreutz, M. R., & Oelschlegel, A. M. (2021) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2021.767384 · Cited by 19
“…synaptic scaling, or the regulation of intrinsic excitability (Zhang and Linden, 2003; Frick and Johnston, 2005; Niethard et al., 2017), in order to maintain stable function while at the same time preserving the specificity of synaptic changes that encode information (Turrigiano, 2012, 2017).”
BackgroundChariker, L., Shapley, R., Hawken, M., & Young, L.-S. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.2145-21.2022 · Cited by 19
Metaplasticity: a key to visual recovery from amblyopia in adulthood?
Leet, M. P., Bear, M. F., & Gaier, E. D. (2022) · Current Opinion in Ophthalmology · doi:10.1097/icu.0000000000000901 · Cited by 16
“Thus, it has long been recognized that some form of higher-order, homeostatic plasticity is also required to keep synaptic strengths within aphysiologic range [33].”
BackgroundFlores‐Muñoz, C., García-Rojas, F., Pérez, M. A., Santander, O., Mery, E., Ordenes, S., Illanes-González, J., López-Espíndola, D., González‐Jamett, A. M., Fuenzalida, M., et al. (2022) · Cells · doi:10.3390/cells11223646 · Cited by 18
Bielczyk, N., Buitelaar, J. K., Glennon, J. C., & Tiesinga, P. H. E. (2015) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2015.00029 · Cited by 18
Kolodny, T., Schallmo, M., Gerdts, J. A., Bernier, R., & Murray, S. O. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.2376-19.2020 · Cited by 17
“This possibility is consistent with homeostatic mechanisms that are known to modulate excitation around a set point (Turrigiano, 2011, 2012; Gainey and Feldman, 2017), and hypothesized to be altered in ASD (Ramocki and Zoghbi, 2008; Nelson and Valakh, 2015).”
BackgroundMolecular Diversity of Glutamatergic and GABAergic Synapses from Multiplexed Fluorescence Imaging
Danielson, E., de Arce, K. P., Cimini, B. A., Wamhoff, E., Singh, S., Cottrell, J. R., Carpenter, A. E., & Bathe, M. (2020) · eNeuro · doi:10.1523/eneuro.0286-20.2020 · Cited by 17
Retinal glial remodeling by FGF21 preserves retinal function during photoreceptor degeneration
Fu, Z., Qiu, C., Cagnone, G., Tomita, Y., Huang, S., Cakir, B., Kotoda, Y., Allen, W., Bull, E., Akula, J. D., et al. (2021) · iScience · doi:10.1016/j.isci.2021.102376 · Cited by 19
“However, homeostatic plasticity studies in the CNS suggests that neurons may regulate dendritic and axonal connectivity, as well as intrinsic excitability in response to perturbations in order to stabilize function (Tien and Kerschensteiner, 2018; Turrigiano, 2012).”
BackgroundThe influence of sensory experience on the glutamatergic synapse
Cooper, D. D., & Frenguelli, B. G. (2021) · Neuropharmacology · doi:10.1016/j.neuropharm.2021.108620 · Cited by 19
Blanqué, A., Repetto, D., Rohlmann, A., Brockhaus, J., Duning, K., Pavenstädt, H. J., Wolff, I., & Missler, M. (2015) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2015.00013 · Cited by 18
Lopez, C. M., Pelkey, K. A., Chittajallu, R., Nakashiba, T., Tóth, K., Tonegawa, S., & McBain, C. J. (2012) · Frontiers in Neural Circuits · doi:10.3389/fncir.2012.00085 · Cited by 18
“However, it remains possible that the silenced old GCs undergo other homeostatically induced changes due to altered participation within the circuit (Desai, 2003; Davis, 2006; Turrigiano, 2012).”
BackgroundRen, B., Yuan, Q., Cha, S., Liu, S.-Y. M., Zhang, J., & Guo, G. (2025) · Molecular Neurobiology · doi:10.1007/s12035-025-05152-5 · Cited by 21
“…plasticity maintains the overall neuronal stability by a series of regulatory mechanisms such as global structural synaptic scaling (neurons adjust the strength of all their synapses to stabilize the overall firing (reviewed in [229]) and intrinsic excitability regulation (reviewed in [230]).”
Neurocoagulation from a Mechanistic Point of View in the Central Nervous System
Stein, E. S., Berkowitz, S. H., Gofrit, S. G., Altman, K., Weinberg, N., & Maggio, N. (2022) · Seminars in Thrombosis and Hemostasis · doi:10.1055/s-0041-1741569 · Cited by 17
A glutamate receptor C-tail recruits CaMKII to suppress retrograde homeostatic signaling
Perry, S., Han, Y., Qiu, C., Chien, C., Goel, P., Nishimura, S., Sajnani, M. R., Schmid, A., Sigrist, S. J., & Dickman, D. K. (2022) · Nature Communications · doi:10.1038/s41467-022-35417-9 · Cited by 20
Schröder, J. K., Abdel‐Hafiz, L., Ali, A. A. H., Cousin, T. C., Hallenberger, J., Almeida, F. R., Anstötz, M., Lenz, M., Vlachos, A., von Gall, C., et al. (2023) · Cells · doi:10.3390/cells12131758 · Cited by 19
“This compensatory adjustment is achieved, at least in part, through changes in the GluR1 subunit of postsynaptic AMPA glutamate receptors (GluR) [19–21], presumably via calcium-dependent negative feedback mechanisms [19,22].”
BackgroundAltered synaptic homeostasis: a key factor in the pathophysiology of depression
Wang, B., He, T., Qiu, G., Li, C., Xue, S., Zheng, Y., Wang, T., Xia, Y., Yao, L., Yan, J., et al. (2025) · Cell & Bioscience · doi:10.1186/s13578-025-01369-y · Cited by 19
“Homeostatic regulation of postsynaptic neurotransmitter receptors, termed synaptic scaling, involves the bi-directional regulation of the amplitude of mEPSCs to counterbalance chronic alterations in neuronal activity [149, 150].”
Ito, A., Kakegawa, W., Kohda, K., Miura, E., Okabe, S., & Yuzaki, M. (2014) · European Journal of Neuroscience · doi:10.1111/ejn.12487 · Cited by 17
“In many neuronal circuits, the activities of inhibitory and excitatory neurons are balanced at the network level by homeostatic plasticity (Turrigiano, 2012).”
BackgroundLamanna, J., Signorini, M. G., Cerutti, S., & Malgaroli, A. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00044 · Cited by 17
“…fractal features might represent a communication channel for the presynaptic compartment to inform the postsynaptic neuron about its state (e.g., its release probability), even when the average release rate is scaled up or down by other homeostatic phenomena (Pozo and Goda, 2010; Turrigiano, 2012).”
InfluentialNovel concepts in sleep regulation
Wigren, H., & Porkka‐Heiskanen, T. (2017) · Acta Physiologica · doi:10.1111/apha.13017 · Cited by 21
“Homeostasis of neuronal firing both at neuronal network and at single neurone level has been described, as well as synaptic homeostasis.(7,8) Extra- and intracellular ion concentrations and glucose level, as well as temperature, are classical targets for homeostatic regulation, and it is clear that these homeostases n…”
BackgroundFiring Rate Homeostasis Can Occur in the Absence of Neuronal Activity-Regulated Transcription
Tyssowski, K. M., Letai, K. C., Rendall, S., Tan, C., Nizhnik, A., Kaeser, P. S., & Gray, J. M. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.1108-19.2019 · Cited by 18
“Importantly, each of these transcription-dependent forms of homeostatic plasticity— synaptic scaling, changing E/I balance, and changing intrinsic excitability— can alter firing rates and are thus leading candidate mechanisms underlying firing rate homeostasis (Turrigiano, 2012).”
BackgroundSynaptic Vesicles Dynamics in Neocortical Epilepsy
Vannini, E., Restani, L., Dilillo, M., McDonnell, L. A., Caleo, M., & Marra, V. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.606142 · Cited by 17
“When network activity is tipped out of balance, a number of cellular processes take place to re-establish its normal function (Turrigiano, 2012).”
BackgroundNeuronal Activity and Its Role in Controlling Antioxidant Genes
Qiu, J., Dando, O., Febery, J. A., Fowler, J. H., Chandran, S., & Hardingham, G. E. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21061933 · Cited by 17
Lebedev, A. V., Nilsson, J., Lindström, J., Fredborg, W., Akenine, U., Hillilä, C., Andersen, P., Spulber, G., de Lange, E. C. M., van den Berg, D.-J., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-62172-y · Cited by 18
Pervasive compartment-specific regulation of gene expression during homeostatic synaptic scaling
Colameo, D., Rajman, M., Soutschek, M., Bicker, S., von Ziegler, L., Bohacek, J., Winterer, J., Germain, P., Dieterich, C., & Schratt, G. M. (2021) · EMBO Reports · doi:10.15252/embr.202052094 · Cited by 15
“A major outcome of our study was the observation that PTX treatment induces (Turrigiano, 2012), but a clear picture of how homeostatic feedback is structured at the molecular level has not yet emerged.”
Koene, L. M. C., Niggl, E., Wallaard, I., Onori, M. P., Rotaru, D. C., & Elgersma, Y. (2021) · JCI Insight · doi:10.1172/jci.insight.150120 · Cited by 17
“Conversely, changes in excitability can lead to homeostatic changes in synaptic transmission (24).”
BackgroundTaylor, C. J., Ohline, S. M., Moss, T. J. M., Ulrich, K., & Abraham, W. C. (2016) · European Journal of Neuroscience · doi:10.1111/ejn.13167 · Cited by 19
“The inability to sustain the EE effect on cell excitability may reflect adjustments by cells to maintain homeostasis (Eckert & Abraham, 2010; Turrigiano, 2012).”
BackgroundRem2 stabilizes intrinsic excitability and spontaneous firing in visual circuits
Moore, A. R., Richards, S. E. V., Kenny, K., Royer, L. O., Chan, U., Flavahan, K., Hooser, S. D. V., & Paradis, S. (2018) · eLife · doi:10.7554/elife.33092 · Cited by 17
Metadata
- Authors
- Turrigiano, G.
- Affiliations
- Brandeis University (US)
- Corresponding author
- Turrigiano, G.
- ORCID
- Turrigiano, G.
- Venue
- Cold Spring Harbor Perspectives in Biology
- Publisher
- Cold Spring Harbor Laboratory
- Published
- 2011-11-15
- Volume
- 4
- Issue
- 1
- Pages
- a005736-a005736
- ISSN
- 1943-0264 (ISSN-L)
- PMC
- PMC3249629
- OpenAlex
- W2115900486
- Semantic Scholar
- a5724cd9f8c115624f0538915997ae22b3136e77
- Cited by
- 1,139
- References
- 110
- Citations by year
- 2026: 95 · 2025: 98 · 2024: 82 · 2023: 92 · 2022: 91 · 2021: 107 · 2020: 92 · 2019: 80 · 2018: 77 · 2017: 89 · 2016: 59 · 2015: 69 · 2014: 41 · 2013: 51 · 2012: 15
- Type
- posted content
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Cold Spring Harbor Perspectives in Biology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (submittedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Keywords
- homeostatic plasticity, synaptic scaling, glutamate receptor trafficking, excitation-inhibition balance, neuronal firing rate
- MeSH terms
- Animals, Homeostasis, Humans, Nerve Net, Neuromuscular Junction, Neuronal Plasticity, Neurons, Synapses
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