Otx2 Binding to Perineuronal Nets Persistently Regulates Plasticity in the Mature Visual Cortex
Open accessAbstract
Specific transfer of (orthodenticle homeobox 2) Otx2 homeoprotein into GABAergic interneurons expressing parvalbumin (PV) is necessary and sufficient to open, then close, a critical period (CP) of plasticity in the developing mouse visual cortex. The accumulation of endogenous Otx2 in PV cells suggests the presence of specific Otx2 binding sites. Here, we find that perineuronal nets (PNNs) on the surfaces of PV cells permit the specific, constitutive capture of Otx2. We identify a 15 aa domain containing an arginine-lysine doublet (RK peptide) within Otx2, bearing prototypic traits of a glycosaminoglycan (GAG) binding sequence that mediates Otx2 binding to PNNs, and specifically to chondroitin sulfate D and E, with high affinity. Accordingly, PNN hydrolysis by chondroitinase ABC reduces the amount of endogenous Otx2 in PV cells. Direct infusion of RK peptide similarly disrupts endogenous Otx2 localization to PV cells, reduces PV and PNN expression, and reopens plasticity in adult mice. The closure of one eye during this transient window reduces cortical acuity and is specific to the RK motif, as an Alanine-Alanine variant or a scrambled peptide fails to reactivate plasticity. Conversely, this transient reopening of plasticity in the adult restores binocular vision in amblyopic mice. Thus, one function of PNNs is to facilitate the persistent internalization of Otx2 by PV cells to maintain CP closure. The pharmacological use of the Otx2 GAG binding domain offers a novel, potent therapeutic tool with which to restore cortical plasticity in the mature brain.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
Across multiple neuropsychiatric disorders, including autism, schizophrenia, and bipolar disorder, the developmental gene expression program in PV cells is immature.
“Across multiple neuropsychiatric disorders, including autism, schizophrenia, and bipolar disorder, the developmental gene expression program in PV cells is instead immature (54).”
From Perineuronal nets protect fast-spiking interneurons against oxidative stress (2013) · cites this paper as [54]
The Discussion (page unavailable) proposes that therapies targeting Otx2 transfer into PV circuits might apply to autism spectrum disorders and schizophrenia, which it describes as having a similar cellular etiology. It does not report an immature developmental gene-expression program in PV cells in those disorders, and it does not mention bipolar disorder in this context. (LLM, conf=0.82)
Experimental — accuracy not yet measuredOTX2 and Sema3A bind to 4,6 disulphated GAGs in PNNs, while Nptx2 binds to both 4,6 sulphated GAGs and HA.
“While OTX2 and Sema3A bind to 4,6 disulphated GAGs in the PNNs [23, 28], Nptx2 binds to both 4,6 sulphated GAGs and HA [29].”
From The extracellular matrix and perineuronal nets in memory (2022) · cites this paper as [23]
Soluble transcription factor OTX2 binds to PNNs and is internalised, leading to maturation of PV neurons and maintenance of PNNs in adulthood.
“The soluble transcription factor OTX2 binds to PNNs and is internalised, leading to maturation of PV neurons and maintenance of PNNs in adulthood [23, 26].”
From The extracellular matrix and perineuronal nets in memory (2022) · cites this paper as [23]
Otx-2 maintains PNNs.
“Otx--2, which maintains PNNs (Beurdeley et al., 2012;Bernard and Prochiantz, 2016)”
From Casting a Wide Net: Role of Perineuronal Nets in Neural Plasticity (2016) · cites this paper as Beurdeley et al., 2012
Compromised PNNs prevent persistent uptake of Otx2 homeoprotein into enwrapped PV cells needed for their maturation, including PNN maintenance.
“Compromised PNNs prevent the persistent uptake of Otx2 homeoprotein into the enwrapped PV-cells needed for their maturation (including PNN maintenance itself) (27, 40, 41).”
From Prolonged Period of Cortical Plasticity upon Redox Dysregulation in Fast-Spiking Interneurons (2015) · cites this paper as [41]
Inability to engage downstream molecular pathways by Otx2 within the PV cell would retain a juvenile plastic state.
“Subsequent inability to engage downstream molecular pathways by Otx2 within the PV-cell would retain a juvenile plastic state (41).”
From Prolonged Period of Cortical Plasticity upon Redox Dysregulation in Fast-Spiking Interneurons (2015) · cites this paper as [41]
PNN disruption prevents persistent uptake of Otx2 homeoprotein into enwrapped PV cells required for their maintenance.
“Second, PNN disruption prevents the persistent uptake of Otx2 homeoprotein into the enwrapped PV-cells required for their maintenance (27, 40, 41) (Fig. S3).”
From Prolonged Period of Cortical Plasticity upon Redox Dysregulation in Fast-Spiking Interneurons (2015) · cites this paper as [41]
This convergence may offer novel strategies or drug targets for correcting aberrant brain plasticity in mental illness.
“This may offer novel strategies or drug targets, in addition to antioxidants (18, 25) or Otx2 up-regulation (41, 51), for correcting aberrant brain plasticity in mental illness.”
From Prolonged Period of Cortical Plasticity upon Redox Dysregulation in Fast-Spiking Interneurons (2015) · cites this paper as [41]
The second Otx2 threshold is reversible because decreasing Otx2 concentration engages the plastic regime.
“Importantly, the second threshold is ‘reversible’ as decreasing Otx2 concentration engages the plastic regime (this study; (Beurdeley et al., 2012)).”
From Choroid-Plexus-Derived Otx2 Homeoprotein Constrains Adult Cortical Plasticity (2013) · cites this paper as Beurdeley et al., 2012
Early sensory experience initiates expression of Otx2 binding sites on nascent perineuronal nets, facilitating Otx2 import and opening a period of plasticity.
“The model also stipulates that early sensory experience (sensory input) initiates expression of Otx2 binding sites on nascent PNNs (Beurdeley et al., 2012; Miyata et al., 2012), facilitating Otx2 import and opening a period of plasticity.”
From Choroid-Plexus-Derived Otx2 Homeoprotein Constrains Adult Cortical Plasticity (2013) · cites this paper as Beurdeley et al., 2012
A general source, through mature fully assembled perineuronal nets, participates in maintaining a non-plastic state, allowing the possibility to reopen plasticity in adulthood.
“The same scheme also explain show a general source, thanks to mature, fully assembled PNNs, participates in maintaining a non-plastic state, allowing for the possibility to reopen plasticity in adulthood (Beurdeley et al., 2012; Pizzorusso et al., 2002).”
From Choroid-Plexus-Derived Otx2 Homeoprotein Constrains Adult Cortical Plasticity (2013) · cites this paper as Beurdeley et al., 2012
Permanent transfer of Otx2 through perineuronal net recognition is necessary to repress plasticity in the adult.
“and that the permanent transfer of Otx2 through PNN recognition is necessary to repress plasticity in the adult (Beurdeley et al., 2012).”
From Choroid-Plexus-Derived Otx2 Homeoprotein Constrains Adult Cortical Plasticity (2013) · cites this paper as Beurdeley et al., 2012
Once formed, PNNs control neuronal access to growth and transcription factors, stabilize synaptic connectivity and compartmentalize the neuronal surface, regulating availability of glutamatergic receptors and neuronal firing properties.
“Once formed, and throughout adulthood, PNNs control neuronal access to growth and transcription factors, stabilize synaptic connectivity and compartmentalize the neuronal surface, regulating the availability of glutamatergic receptors to postsynaptic specializations and, thus, neuronal firing properties.23, 25, 38”
From Aggrecan and chondroitin-6-sulfate abnormalities in schizophrenia and bipolar disorder: a postmortem study on the amygdala (2015) · cites this paper as [38]
PNNs have been proposed as indispensable mediators of the modulation of synaptic plasticity by the transcription factor Otx2.
“Interestingly, PNNs have been proposed as indispensable mediators of the modulation of synaptic plasticity by the transcription factor Otx259–61.”
From Elimination of the four extracellular matrix molecules tenascin-C, tenascin-R, brevican and neurocan alters the ratio of excitatory and inhibitory synapses (2019) · cites this paper as [59]
PV and PNN colocalization is correlated with critical period closure and reduced synaptic plasticity, particularly in sensory cortices.
“In fact, PV and PNN colocalization is correlated with critical period closure and reduced synaptic plasticity, particularly in sensory cortices (Nowicka et al., 2009; Beurdeley et al., 2012).”
From The Perineuronal ‘Safety’ Net? Perineuronal Net Abnormalities in Neurological Disorders (2018) · cites this paper as Beurdeley et al., 2012
PNNs are necessary for the uptake of Otx2 by PV cells, which promotes PV cell maturation.
“PNNs are necessary for the uptake of Otx2 by PV cells, which promotes PV cell maturation (Beurdeley et al., 2012).”
From The Perineuronal ‘Safety’ Net? Perineuronal Net Abnormalities in Neurological Disorders (2018) · cites this paper as Beurdeley et al., 2012
Otx2 is localized to GABAergic cells, and is more likely found in PV cells that are enwrapped with PNNs, which contain a specific Otx2 binding site.
“Studies of rodent visual cortex development indicate that Otx2 is localized to GABAergic cells, and is more likely found in PV cells that are enwrapped with PNNs, which contain a specific Otx2 binding site (Beurdeley et al., 2012).”
From The Perineuronal ‘Safety’ Net? Perineuronal Net Abnormalities in Neurological Disorders (2018) · cites this paper as Beurdeley et al., 2012
PNNs regulate synaptic functions and plasticity during development and adulthood.
“Long believed to be responsible primarily for structural support, PNNs have in recent years come to the forefront of neuroscience research as critical elements regulating synaptic functions and plasticity during development and adulthood (Beurdeley et al., 2012; Dityatev et al., 2010; Gogolla et al., 2009; Gundelfinger et al., 2010; Pizzorusso et al., 2002; Xue et al., 2014; Yamada and Jinno, 2013”
From Losing the sugar coating: Potential impact of perineuronal net abnormalities on interneurons in schizophrenia (2015) · cites this paper as Beurdeley et al., 2012
Otx2 signals maturation of parvalbumin-containing GABAergic interneurons, contributing to opening and possibly closure of the critical period.
“this homeoprotein signals the maturation of the parvalbumin-containing GABAergic interneurons, which contributes to the opening and possibly also the closure of the critical period”
From Perineuronal nets and schizophrenia: The importance of neuronal coatings (2014) · cites this paper as Beurdeley et al., 2012
PNNs play a role in capture of Otx2 from thalamic inputs to visual cortex.
“the PNN to play a role in the “capture” of the homeodeomain transcription factor orthodenticle homeobox 2 (Otx2) from thalamic inputs to visual cortex (Beurdeley et al., 2012)”
From Perineuronal nets and schizophrenia: The importance of neuronal coatings (2014) · cites this paper as Beurdeley et al., 2012
Perineuronal nets permit Otx2 capture and transfer into GABAergic interneurons expressing parvalbumin.
“Namely, PNNs permit Otx2 capture and transfer into GABAergic interneurons expressing parvalbumin.”
From The hyaluronan and proteoglycan link proteins: Organizers of the brain extracellular matrix and key molecules for neuronal function and plasticity (2015) · cites this paper as Beurdeley et al., 2012
The maturation and phenotypic maintenance of parvalbumin interneurons require incorporation of the non-cell autonomous homeobox protein Otx2 through its affinity with perineuronal nets.
“Indeed, the maturation and phenotypic maintenance of PVI require incorporation of a non-cell autonomous homeobox protein, Otx2, through its affinity with PNN (Beurdeley et al., 2012; Miyata et al., 2012).”
From Redox dysregulation, neuroinflammation, and NMDA receptor hypofunction: A “central hub” in schizophrenia pathophysiology? (2016) · cites this paper as Beurdeley et al., 2012
PNNs facilitate the capture and uptake of the transcription factor Otx2.
“PNNs also facilitate the capture and uptake of the transcription factor Otx2, which in turn promotes PVBC maturation as well as further PNN development (100, 173, 912, 1063).”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [100]
Otx2 promotes PVBC maturation as well as further PNN development.
“PNNs also facilitate the capture and uptake of the transcription factor Otx2, which in turn promotes PVBC maturation as well as further PNN development (100, 173, 912, 1063).”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [100]
Blocking the ability of Otx2 to bind to PNNs results in their degradation and reopens the critical period in adults.
“Similarly, blocking the ability of Otx2 to bind to PNNs results in their degradation and reopens the critical period in adults (100).”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [100]
Removing PNNs or lowering Otx2 uptake reopens plasticity in adult animals.
“In contrast, removing PNNs or reducing Otx2 uptake reopens plasticity in adulthood (Beurdeley et al., 2012; Pizzorusso et al., 2002; Spatazza et al., 2013).”
From Clock Genes Control Cortical Critical Period Timing (2015) · cites this paper as Beurdeley et al., 2012
PNN condensation helps close critical-period plasticity.
“which in turn contributes to closure of critical period plasticity (Beurdeley et al., 2012; Carulli et al., 2010; Pizzorusso et al., 2002).”
From Clock Genes Control Cortical Critical Period Timing (2015) · cites this paper as Beurdeley et al., 2012
As PV-cells mature, PNNs of extracellular matrix molecules condense around their cell bodies.
“With PV-cell maturation, perineuronal nets (PNNs) of extracellular matrix molecules condense around their somata”
From Clock Genes Control Cortical Critical Period Timing (2015) · cites this paper as Beurdeley et al., 2012
The maturation of PNNs in the developing cortex coincides with the closure of the critical periods of synaptogenesis and circuit refinement.
“The maturation of PNNs in the developing cortex coincides with the closure of the critical periods of synaptogenesis and circuit refinement (Beurdeley et al., 2012; Ye and Miao, 2013).”
From Adult neurogenesis, glia, and the extracellular matrix (2019) · cites this paper as Beurdeley et al., 2012
PNNs limit plasticity and are responsible for the closure of the critical period for ocular dominance in the visual cortex.
“PNNs are thought to limit plasticity and are responsible for the closure of the critical period for ocular dominance in the visual cortex (28).”
From Perineuronal nets, inhibitory interneurons and anxiety-related ventral hippocampal neuronal oscillations are altered by early life adversity (2019) · cites this paper as [28]
OTX2 produced in the choroid plexus binds to PNNs in the visual cortex where it facilitates the expression of PNNs.
“OTX2 produced in the choroid plexus binds to PNNs in the visual cortex where it facilitates the expression of PNNs (28).”
From Perineuronal nets, inhibitory interneurons and anxiety-related ventral hippocampal neuronal oscillations are altered by early life adversity (2019) · cites this paper as [28]
Continual binding of OTX2 to PNNs is necessary for synaptic stability in the adult visual cortex.
“Continual binding of OTX2 to PNNs has been shown to be necessary for synaptic stability in the adult visual cortex and blocking OTX2 uptake into PV+ cells in adults has been demonstrated to reduce PNN expression and reinstate juvenile levels of plasticity (28).”
From Perineuronal nets, inhibitory interneurons and anxiety-related ventral hippocampal neuronal oscillations are altered by early life adversity (2019) · cites this paper as [28]
Blocking OTX2 uptake into PV+ cells in adults reduces PNN expression and reinstates juvenile levels of plasticity.
“Continual binding of OTX2 to PNNs has been shown to be necessary for synaptic stability in the adult visual cortex and blocking OTX2 uptake into PV+ cells in adults has been demonstrated to reduce PNN expression and reinstate juvenile levels of plasticity (28).”
From Perineuronal nets, inhibitory interneurons and anxiety-related ventral hippocampal neuronal oscillations are altered by early life adversity (2019) · cites this paper as [28]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Critical period plasticity in local cortical circuits
Hensch, T. K. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1787 · Cited by 2,323 · see citing works
Self-citationCortical inhibitory neurons and schizophrenia
Lewis, D. A., Hashimoto, T., & Volk, D. W. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1648 · Cited by 2,297 · see citing works
Reactivation of Ocular Dominance Plasticity in the Adult Visual Cortex
Pizzorusso, T., Medini, P., Berardi, N., Chierzi, S., Fawcett, J. W., & Maffei, L. (2002) · Science · doi:10.1126/science.1072699 · Cited by 1,679 · see citing works
Molecular modeling of protein-glycosaminoglycan interactions.
Cardin, A. D., & Weintraub, H. J. R. (1989) · Arteriosclerosis An Official Journal of the American Heart Association Inc · doi:10.1161/01.atv.9.1.21 · Cited by 1,301 · see citing works
Hensch, T. K. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.27.070203.144327 · Cited by 1,300 · see citing works
Self-citationWiesel, T. N., & Hubel, D. H. (1963) · Journal of Neurophysiology · doi:10.1152/jn.1963.26.6.978 · Cited by 1,291 · see citing works
Experience-Dependent Plasticity of Binocular Responses in the Primary Visual Cortex of the Mouse
Gordon, J. A., & Stryker, M. P. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-10-03274.1996 · Cited by 856 · see citing works
Perineuronal Nets Protect Fear Memories from Erasure
Gogolla, N., Caroni, P., Lüthi, A., & Herry, C. (2009) · Science · doi:10.1126/science.1174146 · Cited by 760 · see citing works
Antennapedia homeobox peptide regulates neural morphogenesis.
Joliot, A., Pernelle, C., Bazin, H., & Prochiantz, A. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.5.1864 · Cited by 653 · see citing works
Self-citationCommon circuit defect of excitatory-inhibitory balance in mouse models of autism
Gogolla, N., LeBlanc, J. J., Quast, K. B., Südhof, T. C., Fagiolini, M., & Hensch, T. K. (2009) · Journal of Neurodevelopmental Disorders · doi:10.1007/s11689-009-9023-x · Cited by 610 · see citing works
Self-citationRemoving brakes on adult brain plasticity: From molecular to behavioral interventions
Bavelier, D., Levi, D. M., Li, R. W., Dan, Y., & Hensch, T. K. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.4812-10.2010 · Cited by 589 · see citing works
Self-citationSynaptic basis for intense thalamocortical activation of feedforward inhibitory cells in neocortex
Cruikshank, S. J., Lewis, T. J., & Connors, B. W. (2007) · Nature Neuroscience · doi:10.1038/nn1861 · Cited by 558 · see citing works
Animals lacking link protein have attenuated perineuronal nets and persistent plasticity
Carulli, D., Pizzorusso, T., Kwok, J. C. F., Putignano, E., Poli, A., Forostyak, S., Andrews, M. R., Deepa, S. S., Glant, T. T., & Fawcett, J. W. (2010) · Brain · doi:10.1093/brain/awq145 · Cited by 495 · see citing works
Transduction peptides: from technology to physiology
Joliot, A., & Prochiantz, A. (2004) · Nature Cell Biology · doi:10.1038/ncb0304-189 · Cited by 495 · see citing works
Self-citationSugiyama, S., Di Nardo, A. A., Aizawa, S., Matsuo, I., Volovitch, M., Prochiantz, A., & Hensch, T. K. (2008) · Cell · doi:10.1016/j.cell.2008.05.054 · Cited by 491 · cited 21× · see citing works
“Otx2 persists throughout life in PV cells, and its capture is dependent on visual input (Sugiyama et al., 2008).”
BackgroundMethodInfluentialSelf-citationHolmes, J. M., & Clarke, M. W. (2006) · The Lancet · doi:10.1016/s0140-6736(06)68581-4 · Cited by 425 · see citing works
Perineuronal nets — a specialized form of extracellular matrix in the adult nervous system
Celio, M. R., & Blümcke, I. (1994) · Brain Research Reviews · doi:10.1016/0165-0173(94)90006-x · Cited by 386 · see citing works
Experience-dependent pruning of dendritic spines in visual cortex by tissue plasminogen activator
Mataga, N., Mizuguchi, Y., & Hensch, T. K. (2004) · Neuron · doi:10.1016/j.neuron.2004.11.028 · Cited by 371 · see citing works
Self-citationStructural and functional recovery from early monocular deprivation in adult rats
Pizzorusso, T., Medini, P., Landi, S., Baldini, S., Berardi, N., & Maffei, L. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0602657103 · Cited by 367 · see citing works
Lynx1, a Cholinergic Brake, Limits Plasticity in Adult Visual Cortex
Morishita, H., Miwa, J. M., Heintz, N., & Hensch, T. K. (2010) · Science · doi:10.1126/science.1195320 · Cited by 365 · see citing works
Self-citationPersistent cortical plasticity by upregulation of chondroitin 6-sulfation
Miyata, S., Komatsu, Y., Yoshimura, Y., Taya, C., & Kitagawa, H. (2012) · Nature Neuroscience · doi:10.1038/nn.3023 · Cited by 365 · see citing works
The Molecular Diversity of Glycosaminoglycans Shapes Animal Development
Bülow, H. E., & Hobert, O. (2006) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.22.010605.093433 · Cited by 340 · see citing works
Härtig, W., Derouiche, A., Welt, K., Brauer, K., Grosche, J., Mäder, M., Reichenbach, A., & Brückner, G. (1999) · Brain Research · doi:10.1016/s0006-8993(99)01784-9 · Cited by 339 · see citing works
Cheng, H.-J., & Flanagan, J. G. (1994) · Cell · doi:10.1016/0092-8674(94)90408-1 · Cited by 335 · see citing works
Critical period revisited: impact on vision
Morishita, H., & Hensch, T. K. (2008) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2008.05.009 · Cited by 311 · see citing works
Self-citationThe transcription factor Engrailed-2 guides retinal axons
Brunet, I., Weinl, C., Piper, M., Trembleau, A., Volovitch, M., Harris, W. A., Prochiantz, A., & Holt, C. E. (2005) · Nature · doi:10.1038/nature04110 · Cited by 264 · see citing works
Self-citationZiegler, A. (2007) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2007.10.005 · Cited by 254 · see citing works
The effect of dark rearing on the time course of the critical period in cat visual cortex
Mower, G. D. (1991) · Developmental Brain Research · doi:10.1016/0165-3806(91)90001-y · Cited by 220 · see citing works
Visual cortex is rescued from the effects of dark rearing by overexpression of BDNF
Gianfranceschi, L., Siciliano, R., Walls, J., Morales, B., Kirkwood, A., Huang, Z. J., Tonegawa, S., & Maffei, L. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1934836100 · Cited by 201 · see citing works
Rapid critical period induction by tonic inhibition in visual cortex
Iwai, Y., Fagiolini, M., Obata, K., & Hensch, T. K. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-17-06695.2003 · Cited by 201 · see citing works
Self-citationBidirectional plasticity in fast-spiking GABA circuits by visual experience
Yazaki-Sugiyama, Y., Kang, S., Câteau, H., Fukai, T., & Hensch, T. K. (2009) · Nature · doi:10.1038/nature08485 · Cited by 200 · see citing works
Self-citationModulation of Perineuronal Nets and Parvalbumin with Developmental Song Learning
Balmer, T. S., Carels, V. M., Frisch, J. L., & Nick, T. A. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.2974-09.2009 · Cited by 181 · see citing works
Fagiolini, M., Katagiri, H., Miyamoto, H., Mori, H., Grant, S. G. N., Mishina, M., & Hensch, T. K. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0536089100 · Cited by 178 · see citing works
Self-citationAge-Dependent Ocular Dominance Plasticity in Adult Mice
Lehmann, K., & Löwel, S. (2008) · PLoS ONE · doi:10.1371/journal.pone.0003120 · Cited by 175 · see citing works
Extracellular Matrix and Visual Cortical Plasticity
Berardi, N., Pizzorusso, T., & Maffei, L. (2004) · Neuron · doi:10.1016/j.neuron.2004.12.008 · Cited by 163 · see citing works
Gallet, A., Staccini-Lavenant, L., & Thérond, P. P. (2008) · Developmental Cell · doi:10.1016/j.devcel.2008.03.001 · Cited by 161 · see citing works
alpha-2,8-Polysialic acid is the neuronal surface receptor of antennapedia homeobox peptide.
Joliot, A., Triller, A., Volovitch, M., Pernelle, C., & Prochiantz, A. (1991) · PubMed · Cited by 135 · see citing works
Self-citationZiegler, A., & Seelig, J. (2007) · Biophysical Journal · doi:10.1529/biophysj.107.113472 · Cited by 129 · see citing works
Hensch, T. K., Gordon, J. A., Brandon, E. P., McKnight, G. S., Idzerda, R. L., & Stryker, M. P. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-06-02108.1998 · Cited by 117 · see citing works
Self-citationExtracellular Engrailed Participates in the Topographic Guidance of Retinal Axons In Vivo
Wizenmann, A., Brunet, I., Lam, J. S. Y., Sonnier, L., Beurdeley, M., Zarbalis, K. S., Weisenhorn, D. M. V., Weinl, C., Dwivedy, A., Joliot, A., et al. (2009) · Neuron · doi:10.1016/j.neuron.2009.09.018 · Cited by 117 · see citing works
Self-citationPlasticity in the adult brain: lessons from the visual system
Spolidoro, M., Sale, A., Berardi, N., & Maffei, L. (2009) · Experimental Brain Research · doi:10.1007/s00221-008-1509-3 · Cited by 111 · see citing works
Gordon, J. A., Cioffi, D., Silva, A. J., & Stryker, M. P. (1996) · Neuron · doi:10.1016/s0896-6273(00)80181-6 · Cited by 111 · see citing works
Nowicka, D., Soulsby, S., Skangiel‐Kramska, J., & Glazewski, S. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06996.x · Cited by 110 · see citing works
Extracellular Matrix and Visual Cortical PlasticityFreeing the Synapse
Berardi, N., Pizzorusso, T., & Maffei, L. (2004) · Neuron · doi:10.1016/s0896-6273(04)00796-2 · Cited by 85 · see citing works
Jastrebova, N., Vanwildemeersch, M., Rapraeger, A. C., Giménez‐Gallego, G., Lindahl, U., & Spillmann, D. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m600806200 · Cited by 78 · see citing works
Stettler, O., Joshi, R. L., Wizenmann, A., Reingruber, J., Holcman, D., Bouillot, C., Castagner, F., Prochiantz, A., & Moya, K. L. (2012) · Development · doi:10.1242/dev.063875 · Cited by 67 · see citing works
Self-citationFeldman, D. E. (2000) · Nature Neuroscience · doi:10.1038/73849 · Cited by 61 · see citing works
Erişir, A., & Dreusicke, M. (2005) · The Journal of Comparative Neurology · doi:10.1002/cne.20507 · Cited by 52 · see citing works
The topological role of homeoproteins in the developing central nervous system
Brunet, I., Nardo, A. A. D., Sonnier, L., Beurdeley, M., & Prochiantz, A. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.03.010 · Cited by 52 · see citing works
Self-citationLullo, E. D., Haton, C., Poupon, C. L., Volovitch, M., Joliot, A., Thomas, J., & Prochiantz, A. (2011) · Development · doi:10.1242/dev.066282 · Cited by 45 · see citing works
Self-citationCheng, H.-J., & Flanagan, J. G. (1995) · Trends in Genetics · doi:10.1016/0168-9525(95)90592-8 · Cited by 35 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Hippocampal GABAergic Inhibitory Interneurons
Pelkey, K. A., Chittajallu, R., Craig, M. T., Tricoire, L., Wester, J. C., & McBain, C. J. (2017) · Physiological Reviews · doi:10.1152/physrev.00007.2017 · Cited by 889 · see citing works
Balancing Plasticity/Stability Across Brain Development
Takesian, A. E., & Hensch, T. K. (2013) · Progress in Brain Research · doi:10.1016/b978-0-444-63327-9.00001-1 · Cited by 667 · see citing works
Self-citationThe roles of perineuronal nets and the perinodal extracellular matrix in neuronal function
Fawcett, J. W., Oohashi, T., & Pizzorusso, T. (2019) · Nature Reviews Neuroscience · doi:10.1038/s41583-019-0196-3 · Cited by 589 · see citing works
Perineuronal nets protect fast-spiking interneurons against oxidative stress
Cabungcal, J.-H., Steullet, P., Morishita, H., Kraftsik, R., Cuenod, M., Hensch, T. K., & Do, K. Q. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1300454110 · Cited by 512 · see citing works
Self-citationBiosynthesis and function of chondroitin sulfate
Mikami, T., & Kitagawa, H. (2013) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2013.06.006 · Cited by 505 · see citing works
Critical period regulation across multiple timescales
Reh, R. K., Dias, B. G., Nelson, C. A., Kaufer, D., Werker, J. F., Kolb, B., Levine, J. D., & Hensch, T. K. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1820836117 · Cited by 492 · see citing works
Self-citationCasting a Wide Net: Role of Perineuronal Nets in Neural Plasticity
Sorg, B. A., Berretta, S., Blacktop, J. M., Fawcett, J. W., Kitagawa, H., Kwok, J. C. F., & Miquel, M. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.2351-16.2016 · Cited by 454 · see citing works
GABAergic Interneurons Shape the Functional Maturation of the Cortex
Le Magueresse, C., & Monyer, H. (2013) · Neuron · doi:10.1016/j.neuron.2013.01.011 · Cited by 425 · see citing works
Proteoglycan Chemical Diversity Drives Multifunctional Cell Regulation and Therapeutics
Karamanos, N. K., Piperigkou, Z., Theocharis, A. D., Watanabe, H., Franchi, M., Baud, S., Brézillon, S., Götte, M., Passi, A. G., Vigetti, D., et al. (2018) · Chemical Reviews · doi:10.1021/acs.chemrev.8b00354 · Cited by 372 · see citing works
Lensjø, K. K., Lepperød, M. E., Dick, G., Hafting, T., & Fyhn, M. (2017) · The Journal of Neuroscience · doi:10.1523/jneurosci.2504-16.2016 · Cited by 281 · see citing works
Crosstalk between glia, extracellular matrix and neurons
Song, I., & Dityatev, A. E. (2017) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2017.03.003 · Cited by 263 · see citing works
Steullet, P., Cabungcal, J. H., Monin, A., Dwir, D., O'Donnell, P., Cuenod, M., & Do, K. Q. (2016) · Schizophrenia Research · doi:10.1016/j.schres.2014.06.021 · Cited by 262 · see citing works
Hensch, T. K., & Quinlan, E. M. (2018) · Visual Neuroscience · doi:10.1017/s0952523817000219 · Cited by 256 · see citing works
Self-citationTargeting the neural extracellular matrix in neurological disorders
Soleman, S., Filippov, M. A., Dityatev, A., & Fawcett, J. W. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.08.050 · Cited by 244 · see citing works
Neuronal Plasticity: Beyond the Critical Period
Hübener, M., & Bonhoeffer, T. (2014) · Cell · doi:10.1016/j.cell.2014.10.035 · Cited by 237 · see citing works
Adult neurogenesis, glia, and the extracellular matrix
Cope, E. C., & Gould, E. (2019) · Cell Stem Cell · doi:10.1016/j.stem.2019.03.023 · Cited by 236 · see citing works
Perineuronal Nets: Plasticity, Protection, and Therapeutic Potential
Reichelt, A. C., Hare, D. J., Bussey, T. J., & Saksida, L. M. (2019) · Trends in Neurosciences · doi:10.1016/j.tins.2019.04.003 · Cited by 219 · see citing works
Infantile Amnesia: A Critical Period of Learning to Learn and Remember
Alberini, C. M., & Travaglia, A. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.0324-17.2017 · Cited by 209 · see citing works
Aggrecan Directs Extracellular Matrix-Mediated Neuronal Plasticity
Rowlands, D., Lensjø, K. K., Dinh, T., Yang, S., Andrews, M. R., Hafting, T., Fyhn, M., Fawcett, J. W., & Dick, G. (2018) · The Journal of Neuroscience · doi:10.1523/jneurosci.1122-18.2018 · Cited by 204 · see citing works
GABAA receptors and plasticity of inhibitory neurotransmission in the central nervous system
Fritschy, J., & Panzanelli, P. (2014) · European Journal of Neuroscience · doi:10.1111/ejn.12534 · Cited by 199 · see citing works
Dyck, S. M., & Karimi‐Abdolrezaee, S. (2015) · Experimental Neurology · doi:10.1016/j.expneurol.2015.04.006 · Cited by 189 · see citing works
The extracellular matrix and perineuronal nets in memory
Fawcett, J. W., Fyhn, M., Jendelova, P., Kwok, J. C. F., Ruzicka, J., & Sorg, B. A. (2022) · Molecular Psychiatry · doi:10.1038/s41380-022-01634-3 · Cited by 169 · see citing works
Inhibitory circuit gating of auditory critical-period plasticity
Takesian, A. E., Bogart, L. J., Lichtman, J. W., & Hensch, T. K. (2018) · Nature Neuroscience · doi:10.1038/s41593-017-0064-2 · Cited by 173 · see citing works
Self-citationChoroid-Plexus-Derived Otx2 Homeoprotein Constrains Adult Cortical Plasticity
Spatazza, J., Lee, H. H. C., Di Nardo, A. A., Tibaldi, L., Joliot, A., Hensch, T. K., & Prochiantz, A. (2013) · Cell Reports · doi:10.1016/j.celrep.2013.05.014 · Cited by 176 · see citing works
Self-citationDevelopment and specification of GABAergic cortical interneurons
Kelsom, C., & Lu, W. (2013) · Cell & Bioscience · doi:10.1186/2045-3701-3-19 · Cited by 171 · see citing works
NMDA Receptor Regulation Prevents Regression of Visual Cortical Function in the Absence of Mecp2
Durand, S., Patrizi, A., Quast, K. B., Hachigian, L., Pavlyuk, R., Saxena, A., Carninci, P., Hensch, T. K., & Fagiolini, M. (2012) · Neuron · doi:10.1016/j.neuron.2012.12.004 · Cited by 172 · see citing works
Self-citationMiyata, S., & Kitagawa, H. (2017) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2017.06.010 · Cited by 171 · see citing works
The Perineuronal ‘Safety’ Net? Perineuronal Net Abnormalities in Neurological Disorders
Wen, T. H., Binder, D. K., Ethell, I. M., & Razak, K. A. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00270 · Cited by 170 · see citing works
Toyoizumi, T., Miyamoto, H., Yazaki-Sugiyama, Y., Atapour, N., Hensch, T. K., & Miller, K. D. (2013) · Neuron · doi:10.1016/j.neuron.2013.07.022 · Cited by 158 · see citing works
Self-citationDo, K. Q., Cuenod, M., & Hensch, T. K. (2015) · Schizophrenia Bulletin · doi:10.1093/schbul/sbv065 · Cited by 158 · see citing works
Self-citationVitamin D in Synaptic Plasticity, Cognitive Function, and Neuropsychiatric Illness
Mayne, P., & Burne, T. H. J. (2019) · Trends in Neurosciences · doi:10.1016/j.tins.2019.01.003 · Cited by 162 · see citing works
Fawcett, J. W. (2015) · Progress in brain research · doi:10.1016/bs.pbr.2015.02.001 · Cited by 156 · see citing works
Ye, Q., & Miao, Q.-L. (2013) · Matrix Biology · doi:10.1016/j.matbio.2013.04.001 · Cited by 146 · see citing works
Pantazopoulos, H., Markota, M., Jaquet, F., Ghosh, D., Wallin, A., Santos, A., Caterson, B., & Berretta, S. (2015) · Translational Psychiatry · doi:10.1038/tp.2014.128 · Cited by 153 · see citing works
Berretta, S., Pantazopoulos, H., Markota, M., Brown, C., & Batzianouli, E. T. (2015) · Schizophrenia Research · doi:10.1016/j.schres.2014.12.040 · Cited by 152 · see citing works
Mechanisms of Action and Persistent Neuroplasticity by Drugs of Abuse
Korpi, E. R., den Hollander, B., Farooq, U., Vashchinkina, E., Rajkumar, R., Nutt, D. J., Hyytiä, P., & Dawe, G. S. (2015) · Pharmacological Reviews · doi:10.1124/pr.115.010967 · Cited by 148 · see citing works
The homeobox gene Otx2 in development and disease
Béby, F., & Lamonerie, T. (2013) · Experimental Eye Research · doi:10.1016/j.exer.2013.03.007 · Cited by 148 · see citing works
Perineuronal nets in brain physiology and disease
Testa, D., Prochiantz, A., & Nardo, A. A. D. (2018) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2018.09.011 · Cited by 141 · see citing works
Self-citationChondroitin sulfates and their binding molecules in the central nervous system
Djerbal, L., Lortat-Jacob, H., & Kwok, J. (2017) · Glycoconjugate Journal · doi:10.1007/s10719-017-9761-z · Cited by 144 · see citing works
Lensjø, K. K., Christensen, A. C., Tennøe, S., Fyhn, M., & Hafting, T. (2017) · eneuro · doi:10.1523/eneuro.0379-16.2017 · Cited by 133 · see citing works
Wingert, J. C., & Sorg, B. A. (2021) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2021.673210 · Cited by 129 · see citing works
Brain ageing changes proteoglycan sulfation, rendering perineuronal nets more inhibitory
Foscarin, S., Raha-Chowdhury, R., Fawcett, J. W., & Kwok, J. C. F. (2017) · Aging · doi:10.18632/aging.101256 · Cited by 139 · see citing works
Vo, T., Carulli, D., Ehlert, E., Kwok, J. C. F., Dick, G., Mecollari, V., Moloney, E. B., Neufeld, G., de Winter, F., Fawcett, J. W., et al. (2013) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2013.04.009 · Cited by 138 · see citing works
Perineuronal net digestion with chondroitinase restores memory in mice with tau pathology
Yang, S., Cacquevel, M., Saksida, L. M., Bussey, T. J., Schneider, B. L., Aebischer, P., Melani, R., Pizzorusso, T., Fawcett, J. W., & Spillantini, M. G. (2015) · Experimental Neurology · doi:10.1016/j.expneurol.2014.11.013 · Cited by 138 · see citing works
Semaphorins in Adult Nervous System Plasticity and Disease
Carulli, D., de Winter, F., & Verhaagen, J. (2021) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2021.672891 · Cited by 137 · see citing works
Kim, S. Y., Senatorov, V. V., Morrissey, C. S., Lippmann, K., Vazquez, O. N., Milikovsky, D. Z., Gu, F., Parada, I., Prince, D. A., Becker, A. J., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-07394-3 · Cited by 136 · see citing works
Dzyubenko, E., Gottschling, C., & Faissner, A. (2016) · Neural Plasticity · doi:10.1155/2016/5214961 · Cited by 134 · see citing works
Oohashi, T., Edamatsu, M., Bekku, Y., & Carulli, D. (2015) · Experimental Neurology · doi:10.1016/j.expneurol.2015.09.010 · Cited by 131 · see citing works
Cuénod, M., Steullet, P., Cabungcal, J.-H., Dwir, D., Khadimallah, I., Klauser, P., Conus, P., & Kim, Q. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01374-w · Cited by 129 · see citing works
An Extracellular Perspective on CNS Maturation: Perineuronal Nets and the Control of Plasticity
Carulli, D., & Verhaagen, J. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22052434 · Cited by 123 · see citing works
Impact of Early Life Stress on Reward Circuit Function and Regulation
Hanson, J. L., Williams, A. V., Bangasser, D. A., & Peña, C. J. (2021) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2021.744690 · Cited by 123 · see citing works
Shi, W., Wei, X., Wang, X., Du, S., Liu, W., Song, J., & Wang, Y. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1902680116 · Cited by 122 · see citing works
Early depolarizing GABA controls critical-period plasticity in the rat visual cortex
Deidda, G., Allegra, M., Cerri, C., Naskar, S., Bony, G., Zunino, G., Bozzi, Y., Caleo, M., & Cancedda, L. (2015) · Nature Neuroscience · doi:10.1038/nn.3890 · Cited by 120 · see citing works
In Sickness and in Health: Perineuronal Nets and Synaptic Plasticity in Psychiatric Disorders
Pantazopoulos, H., & Berretta, S. (2015) · Neural Plasticity · doi:10.1155/2016/9847696 · Cited by 118 · see citing works
Murthy, S., Kane, G. A., Katchur, N. J., Lara Mejia, P. S., Obiofuma, G., Buschman, T. J., McEwen, B. S., & Gould, E. (2019) · Biological Psychiatry · doi:10.1016/j.biopsych.2019.02.021 · Cited by 118 · see citing works
Removal of perineuronal nets disrupts recall of a remote fear memory
Thompson, E. H., Lensjø, K. K., Wigestrand, M. B., Malthe-Sørenssen, A., Hafting, T., & Fyhn, M. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1713530115 · Cited by 118 · see citing works
Sigal, Y. M., Bae, H., Bogart, L. J., Hensch, T. K., & Zhuang, X. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1817222116 · Cited by 118 · see citing works
Self-citation“GAG-ing with the neuron”: The role of glycosaminoglycan patterning in the central nervous system
Smith, P. D., Coulson‐Thomas, V. J., Foscarin, S., Kwok, J. C. F., & Fawcett, J. W. (2015) · Experimental Neurology · doi:10.1016/j.expneurol.2015.08.004 · Cited by 112 · see citing works
Membrane Crossing and Membranotropic Activity of Cell-Penetrating Peptides: Dangerous Liaisons?
Walrant, A., Cardon, S., Burlina, F., & Sagan, S. (2017) · Accounts of Chemical Research · doi:10.1021/acs.accounts.7b00455 · Cited by 111 · see citing works
Mossink, B., Negwer, M., Schubert, D., & Nadif Kasri, N. (2021) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-020-03714-5 · Cited by 114 · see citing works
Gottschling, C., Wegrzyn, D., Denecke, B., & Faissner, A. (2019) · Scientific Reports · doi:10.1038/s41598-019-50404-9 · Cited by 111 · see citing works
Cerebellar plasticity and associative memories are controlled by perineuronal nets
Carulli, D., Broersen, R., de Winter, F., Muir, E. M., Mešković, M., de Waal, M., de Vries, S., Boele, H.-J., Canto, C. B., De Zeeuw, C. I., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1916163117 · Cited by 110 · see citing works
Lupori, L., Totaro, V., Cornuti, S., Ciampi, L., Carrara, F., Grilli, E., Viglione, A., Tozzi, F., Putignano, E., Mazziotti, R. M., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112788 · Cited by 106 · see citing works
Beyeler, M., Rokem, A., Boynton, G. M., & Fine, I. (2017) · Journal of Neural Engineering · doi:10.1088/1741-2552/aa795e · Cited by 102 · see citing works
Otx2-PNN interaction to regulate cortical plasticity
Bernard, C., & Prochiantz, A. (2016) · Neural Plasticity · doi:10.1155/2016/7931693 · Cited by 102 · see citing works
Self-citationCross-modal synaptic plasticity in adult primary sensory cortices
Lee, H., & Whitt, J. L. (2015) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2015.08.002 · Cited by 102 · see citing works
Self-citationClock Genes Control Cortical Critical Period Timing
Kobayashi, Y., Ye, Z., & Hensch, T. K. (2015) · Neuron · doi:10.1016/j.neuron.2015.02.036 · Cited by 99 · see citing works
Self-citationYamada, J., Ohgomori, T., & Jinno, S. (2015) · European Journal of Neuroscience · doi:10.1111/ejn.12792 · Cited by 99 · see citing works
Miller, G. M., & Hsieh‐Wilson, L. C. (2015) · Experimental Neurology · doi:10.1016/j.expneurol.2015.08.015 · Cited by 98 · see citing works
Zeiler, S. R., Hubbard, R., Gibson, E. M., Zheng, T., Ng, K., O’Brien, R., & Krakauer, J. W. (2016) · Neurorehabilitation and Neural Repair · doi:10.1177/1545968315624783 · Cited by 97 · see citing works
Davis, M. F., Figueroa Velez, D. X., Guevarra, R. P., Yang, M. C., Habeeb, M., Carathedathu, M. C., & Gandhi, S. P. (2015) · Neuron · doi:10.1016/j.neuron.2015.03.062 · Cited by 97 · see citing works
Perineuronal nets and schizophrenia: The importance of neuronal coatings
Bitanihirwe, B. K. Y., & Woo, T.-U. W. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.03.018 · Cited by 95 · see citing works
Origins of strabismus and loss of binocular vision
Quoc, E. B., & Milleret, C. (2014) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2014.00071 · Cited by 93 · see citing works
Trajectory of Parvalbumin Cell Impairment and Loss of Cortical Inhibition in Traumatic Brain Injury
Hsieh, T.-H., Lee, H. H. C., Hameed, M. Q., Pascual‐Leone, Á., Hensch, T. K., & Rotenberg, A. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw318 · Cited by 95 · see citing works
Self-citationEngrailed homeoprotein blocks degeneration in adult dopaminergic neurons through LINE‐1 repression
de Thé, F.-X. B., Rekaik, H., Pezé-Heidsieck, E., Massiani-Beaudoin, O., Joshi, R. L., Fuchs, J., & Prochiantz, A. (2018) · The EMBO Journal · doi:10.15252/embj.201797374 · Cited by 95 · see citing works
Self-citationBochner, D., Sapp, R. W., Steinmetz, J. D., Zhang, S., Lee, H., Djurisic, M. R., Syken, J., Dan, Y., & Shatz, C. J. (2014) · Science Translational Medicine · doi:10.1126/scitranslmed.3010157 · Cited by 92 · see citing works
Self-citationProlonged Period of Cortical Plasticity upon Redox Dysregulation in Fast-Spiking Interneurons
Morishita, H., Cabungcal, J.-H., Chen, Y., Do, K. Q., & Hensch, T. K. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2014.12.026 · Cited by 92 · see citing works
Self-citationBozzelli, P. L., Alaiyed, S., Kim, E., Villapol, S., & Conant, K. E. (2018) · Neural Plasticity · doi:10.1155/2018/5735789 · Cited by 90 · see citing works
Delays in GABAergic interneuron development and behavioral inhibition after prenatal stress
Lussier, S. J., & Stevens, H. E. (2016) · Developmental Neurobiology · doi:10.1002/dneu.22376 · Cited by 89 · see citing works
Nabel, E. M., & Morishita, H. (2013) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2013.00146 · Cited by 85 · see citing works
Stolp, H. B., Fleiss, B., Arai, Y., Supramaniam, V., Vontell, R., Birtles, S., Yates, A. G., Baburamani, A. A., Thornton, C., Rutherford, M., et al. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.00955 · Cited by 85 · see citing works
Hayani, H., Song, I., & Dityatev, A. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00149 · Cited by 84 · see citing works
The Chemorepulsive Protein Semaphorin 3A and Perineuronal Net-Mediated Plasticity
de Winter, F., Kwok, J. C. F., Fawcett, J. W., Vo, T. T., Carulli, D., & Verhaagen, J. (2016) · Neural Plasticity · doi:10.1155/2016/3679545 · Cited by 84 · see citing works
A Sweet Talk: The Molecular Systems of Perineuronal Nets in Controlling Neuronal Communication
Spijker, H. M. V. ‘., & Kwok, J. C. F. (2017) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2017.00033 · Cited by 82 · see citing works
Molecular signature of extracellular matrix pathology in schizophrenia
Pantazopoulos, H., Katsel, P., Haroutunian, V. H., Chelini, G., Klengel, T., & Berretta, S. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.15009 · Cited by 79 · see citing works
Directing Neuronal Signaling through Cell-Surface Glycan Engineering
Pulsipher, A., Griffin, M. E., Stone, S. E., Brown, J. M., & Hsieh‐Wilson, L. C. (2014) · Journal of the American Chemical Society · doi:10.1021/ja5005174 · Cited by 83 · see citing works
Genetic Otx2 mis-localization delays critical period plasticity across brain regions
Lee, H. H. C., Bernard, C., Ye, Z., Acampora, D., Simeone, A., Prochiantz, A., Di Nardo, A. A., & Hensch, T. K. (2017) · Molecular Psychiatry · doi:10.1038/mp.2017.1 · Cited by 82 · see citing works
Self-citationExtracellular Matrix in Neural Plasticity and Regeneration
Chelyshev, Y. A., Kabdesh, I. M., & Mukhamedshina, Y. O. (2020) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-020-00986-0 · Cited by 76 · see citing works
Sarro, E. C., Sullivan, R. M., & Barr, G. A. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.10.064 · Cited by 77 · see citing works
Mirzadeh, Z., Alonge, K. M., Cabrales, E., Herranz‐Pérez, V., Scarlett, J. M., Brown, J. M., Hassouna, R., Matsen, M. E., Hồng, N. T., García‐Verdugo, J. M., et al. (2019) · Nature Metabolism · doi:10.1038/s42255-018-0029-0 · Cited by 76 · see citing works
Regulation of Perineuronal Nets in the Adult Cortex by the Activity of the Cortical Network
Devienne, G. F., Picaud, S., Cohen, I., Piquet, J., Tricoire, L., Testa, D., Nardo, A. A. D., Rossier, J., Cauli, B., & Lambolez, B. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.0434-21.2021 · Cited by 78 · see citing works
Housset, M., Samuel, A., Ettaiche, M., Bemelmans, A., Béby, F., Billon, N., & Lamonerie, T. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.1099-13.2013 · Cited by 76 · see citing works
Where no synapses go: gatekeepers of circuit remodeling and synaptic strength
Mironova, Y. A., & Giger, R. J. (2013) · Trends in Neurosciences · doi:10.1016/j.tins.2013.04.003 · Cited by 75 · see citing works
Chondroitin Sulfate Is Required for Onset and Offset of Critical Period Plasticity in Visual Cortex
Hou, X., Yoshioka, N., Tsukano, H., Sakai, A., Miyata, S., Watanabe, Y., Yanagawa, Y., Sakimura, K., Takeuchi, K., Kitagawa, H., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-04007-x · Cited by 75 · see citing works
Self-citationMiyata, S., & Kitagawa, H. (2016) · Neural Plasticity · doi:10.1155/2016/1305801 · Cited by 70 · see citing works
Mechanisms for modulation of neural plasticity and axon regeneration by chondroitin sulphate
Miyata, S., & Kitagawa, H. (2014) · The Journal of Biochemistry · doi:10.1093/jb/mvu067 · Cited by 70 · see citing works
Beebe, N. L., Young, J. W., Mellott, J. G., & Schofield, B. R. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.0217-16.2016 · Cited by 71 · see citing works
Richter, R. P., Baranova, N. S., Day, A. J., & Kwok, J. C. F. (2017) · Current Opinion in Structural Biology · doi:10.1016/j.sbi.2017.12.002 · Cited by 71 · see citing works
Chondroitin 6-sulphate is required for neuroplasticity and memory in ageing
Yang, S., Gigout, S., Molinaro, A., Naito-Matsui, Y., Hilton, S., Foscarin, S., Nieuwenhuis, B., Tan, C. L., Verhaagen, J., Pizzorusso, T., et al. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01208-9 · Cited by 70 · see citing works
Homeoprotein Signaling in the Developing and Adult Nervous System
Prochiantz, A., & Nardo, A. A. D. (2015) · Neuron · doi:10.1016/j.neuron.2015.01.019 · Cited by 67 · see citing works
Self-citation
- Authors
- Beurdeley, M., Spatazza, J., Lee, H. H. C., Sugiyama, S., Bernard, C., Di Nardo, A. A., Hensch, T. K., & Prochiantz, A.
- Affiliations
- Collège de France (FR)
- Centre National de la Recherche Scientifique (FR)
- Boston Children's Hospital (US)
- Venue
- Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2012-07-04
- Volume
- 32
- Issue
- 27
- Pages
- 9429-9437
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC3419577
- OpenAlex
- W2040502575
- Cited by
- 398
- References
- 50
- Citations by year
- 2026: 17 · 2025: 25 · 2024: 21 · 2023: 28 · 2022: 22 · 2021: 38 · 2020: 37 · 2019: 38 · 2018: 26 · 2017: 34 · 2016: 22 · 2015: 32 · 2014: 29 · 2013: 26 · 2012: 3
- FWCI
- 9.69
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- other-oa
- Locations
- Journal of Neuroscience (publishedVersion, other-oa)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- HAL (submittedVersion, other-oa)
- Funders
- Agence Nationale de la Recherche
- Croucher Foundation
- Ministry of Education, Science and Technology
- Centre National de la Recherche Scientifique
- National Institutes of Health (DP1OD003699)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
- Keywords
- Otx2, perineuronal nets, critical period, visual cortex plasticity, parvalbumin interneurons, glycosaminoglycan binding, chondroitin sulfate, chondroitinase ABC, amblyopia, binocular vision, homeodomain transcription factor
- MeSH terms
- Age Factors, Animals, Extracellular Matrix, Interneurons, Male, Mice, Inbred C57BL, Neuronal Plasticity, Protein Binding, Visual Cortex, Mice, Otx Transcription Factors, GABAergic Neurons
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review