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Microglia in Alzheimer’s disease
Open accessAbstract
Proliferation and activation of microglia in the brain, concentrated around amyloid plaques, is a prominent feature of Alzheimer’s disease (AD). Human genetics data point to a key role for microglia in the pathogenesis of AD. The majority of risk genes for AD are highly expressed (and many are selectively expressed) by microglia in the brain. There is mounting evidence that microglia protect against the incidence of AD, as impaired microglial activities and altered microglial responses to β-amyloid are associated with increased AD risk. On the other hand, there is also abundant evidence that activated microglia can be harmful to neurons. Microglia can mediate synapse loss by engulfment of synapses, likely via a complement-dependent mechanism; they can also exacerbate tau pathology and secrete inflammatory factors that can injure neurons directly or via activation of neurotoxic astrocytes. Gene expression profiles indicate multiple states of microglial activation in neurodegenerative disease settings, which might explain the disparate roles of microglia in the development and progression of AD pathology.
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TL;DR
This review synthesizes human genetic and cell-biological evidence that microglia play a dual role in Alzheimer's disease: protective early (TREM2-dependent clearance and compaction of Aβ) and harmful later (complement-mediated synapse engulfment, inflammatory cytokine release, and tau pathology spread). The authors propose that the detrimental microglial state emerges later in disease, complicating therapeutic strategies that target microglia.
Key findings
- Human genetics implicate microglia in late-onset AD: over 20 loci associate with AD risk, and most identified risk genes are expressed selectively or preferentially in microglia; apart from APOE, common variants confer only minor effects (∼10–20%) on AD risk.
- The TREM2 R47H variant (carried by <0.5% of most populations) increases AD risk approximately threefold and appears to be a loss-of-function mutation impairing TREM2-mediated microglial activation, ligand binding (apoE, apoJ/CLU), and Aβ uptake; Trem2 knockout exacerbates plaque accumulation at later ages (8+ months) in β-amyloidosis mouse models.
- APOE genotype strongly modulates risk: relative to apoE3, a single apoE4 allele confers approximately threefold increased risk and apoE2 approximately twofold reduced risk; apoE4 appears to reduce Aβ clearance and increase plaque deposition.
- Microglia can be harmful: complement (C1q, C3) and microglia mediate synapse loss in amyloid models, CSF1R-inhibitor microglia depletion protects against synapse loss and rescues behavioral deficits, and microglia are implicated in tau spread; in microglia-depleted brains plaque size increased ∼13% over 1 wk.
- Transcriptional profiling identifies a disease-associated microglial (DAM) state with reduced homeostatic genes (e.g., Cx3cr1, P2ry12, Tmem119) and induced neurodegeneration genes (e.g., Apoe, Axl, Csf1, Clec7a, Cst7, Igf1, Itgax), with subtle two- to threefold increases in Trem2 and Tyrobp mRNAs; DAM induction depends largely on TREM2.
Methods
- Narrative review (Hansen, Hanson, and Sheng) synthesizing human genetics (GWAS and rare-variant studies), mouse model studies, and microglial transcriptomic profiling; no primary data are generated.
- Evidence reviewed includes GWAS-identified AD risk loci (Table 1), TREM2 and other microglial risk genes, complement-pathway and microglia-depletion experiments in amyloid and tau mouse models (Fig. 3), and RNA-sequencing/single-cell studies of microglial activation states.
- The authors integrate these findings into a proposed two-phase model of microglial function in AD pathogenesis.
Limitations
- Stated by the paper: exactly how microglia are involved in the disease mechanism "is not settled"; evidence for microglial-mediated neuronal damage comes "mostly in mouse models"; TREM2 studies in tau models report seemingly conflicting roles (neuroprotective in PS19 vs. neurotoxic in hTau) that the authors attribute partly to analysis at different disease stages; whether the TREM2-dependent transcriptional response is helpful, damaging, or incidental in different disease contexts requires further study.
- Stated by the paper: studies of microglial gene expression in purified microglia or at the single-cell level from AD brains "have lagged behind" mouse work, and there was "surprisingly limited overlap" in aging-regulated microglial genes between human and mouse, underscoring the need for human microglia profiling at different disease stages and genotypes.
- Evident from the text: many mechanistic conclusions rest on mouse models that overexpress mutant APP/PS1 or tau transgenes, and the authors note conflicting complement-pathway results (e.g., C3 knockout/inhibition reported both to provide neuroprotection and to increase amyloid burden), so causal direction in humans remains uncertain.
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In the paper
“a striking feature of the identified risk genes is that the majority of them are expressed selectively or preferentially in microglia relative to other cell types in the brain (Fig. 1 A; Srinivasan et al., 2016; Zhang et al., 2016).”
§ Microglia in Alzheimer’s disease > Human genetic evidence for microglia involvement in late-onset AD
What the sources say
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIn the paper
“In a meta-analysis of microglial transcriptomic profiles from various models of CNS diseases (neurodegenerative, demyelinating, ischemic, infectious, inflammatory, and neoplastic), we identified several modules of coordinately regulated genes, including a neurodegeneration-associated module highly similar to the DAM genes mentioned previously (Friedman et al., 2017).”
§ Microglia in Alzheimer’s disease > Microglial activation states defined by transcriptional profiling
What the sources say
- Not checked yetcites Friedman et al., 2017
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesNone of the sources cited for this claim have been checked yet.
In the paper
“rare genetic variants associated with AD (found by gene sequencing or exome array) have also implicated microglia in determining the risk of AD (Guerreiro et al., 2013; Jonsson et al., 2013; Sims et al., 2017).”
§ Microglia in Alzheimer’s disease > Human genetic evidence for microglia involvement in late-onset AD
What the sources say
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesA 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 broad trend implicates microglial dysfunction as a contributing factor, rather than an attendant feature, of AD pathogenesis.”
§ Microglia in Alzheimer’s disease > Human genetic evidence for microglia involvement in late-onset AD
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In the paper
“Aβ aggregates are much more efficiently taken up by microglia when Aβ is complexed with lipoproteins such as LDL, apoE, and CLU/apoJ (Terwel et al., 2011; Yeh et al., 2016).”
§ Microglia in Alzheimer’s disease > Protective role of TREM2 and microglia in AD > Phagocytosis and clearance of Aβ and cellular debris
What the sources say
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In the paper
“The TREM2 mutation most clearly associated with AD (R47H, carried by <0.5% of most populations) increases the risk of AD approximately threefold (Guerreiro et al., 2013; Jonsson et al., 2013).”
§ Microglia in Alzheimer’s disease > Human genetic evidence for microglia involvement in late-onset AD
What the sources say
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesA 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
“In recent years, however, biological advances stemming from human genetics data have removed any doubt that microglia play an important role in the pathogenesis of AD.”
§ Microglia in Alzheimer’s disease > Introduction
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In the paper
“During normal brain development, mounting evidence indicates that microglia engulf synapses and sculpt synaptic connections via a novel role for complement, a component of the innate immune system that enhances the clearance of microbes or damaged cells by phagocytes (Boulanger, 2009; Stephan et al., 2012; Chung et al., 2015).”
§ Microglia in Alzheimer’s disease > Detrimental activities of microglia in AD > Microglia, complement, and synapse engulfment
What the sources say
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesA 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
“Microglial engulfment of synapses likely varies with different developmental stages, brain regions, and disease states.”
§ Microglia in Alzheimer’s disease > Detrimental activities of microglia in AD > Microglia, complement, and synapse engulfment
Strength:hedged· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesThe 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
“SHIP1 dephosphorylates phosphatidylinositol (3,4,5)-trisphosphate to phosphatidylinositol (3,4)-bisphosphate at the plasma membrane, altering the outcomes of PI3K activation.”
§ Microglia in Alzheimer’s disease > Potential involvement of other AD risk genes in microglial function
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes
- It may state two separate claims as one. 47
In the paper
“Using these modules to probe the single-cell expression data of Keren-Shaul et al. (2017), we revealed a unique subset of microglia, distinct from the DAM cells, that expressed an interferon-related gene module and increased numerically in brains with β-amyloid pathology (Friedman et al., 2017).”
§ Microglia in Alzheimer’s disease > Microglial activation states defined by transcriptional profiling
What the sources say
- Not checked yetcites Friedman et al., 2017
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
“We also review the evidence that, once activated, microglia can have harmful actions in AD, such as being the source of inflammatory factors and mediating the engulfment of neuronal synapses.”
§ Microglia in Alzheimer’s disease > Introduction
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
“In this review, we consider the genetic and cell biological data indicating that microglia have protective functions that restrain the toxic accumulation of β-amyloid and prevent the development of AD.”
§ Microglia in Alzheimer’s disease > Introduction
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“TREM2–ligand interactions are impaired by TREM2 variants that increase AD risk (Wang et al., 2015; Kober et al., 2016; Yeh et al., 2016; Song et al., 2017), implying that these AD variants are at least partial loss-of-function mutants.”
§ Microglia in Alzheimer’s disease > Protective role of TREM2 and microglia in AD
What the sources say
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“TREM2 functions as a cell surface receptor on microglia; via its interaction with the activating adaptor protein DAP12 (encoded by the TYROBP gene), TREM2 stimulation initiates signal transduction pathways that promote microglial chemotaxis, phagocytosis, survival, and proliferation (Takahashi et al., 2005; Hsieh et al., 2009; Kleinberger et al., 2014; Poliani et al., 2015; Wang et al., 2015, 2016”
§ Microglia in Alzheimer’s disease > Protective role of TREM2 and microglia in AD
What the sources say
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“TREM2 is required for microglial phagocytosis of a variety of substrates, including apoptotic neurons, bacteria, LDL and other lipoproteins, and Aβ (Takahashi et al., 2005; N’Diaye et al., 2009; Kleinberger et al., 2014; Atagi et al., 2015; Yeh et al., 2016).”
§ Microglia in Alzheimer’s disease > Protective role of TREM2 and microglia in AD > Phagocytosis and clearance of Aβ and cellular debris
What the sources say
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“The interaction of TREM2 with its lipoprotein ligands (LDL, APOE, and CLU) was impaired by the AD-linked mutations of TREM2 (R47H, R62H, and D87N) and completely abolished by Nasu–Hakola disease–linked mutations (Y38C and T66M; Atagi et al., 2015; Bailey et al., 2015; Yeh et al., 2016).”
§ Microglia in Alzheimer’s disease > Protective role of TREM2 and microglia in AD > Phagocytosis and clearance of Aβ and cellular debris
What the sources say
- Not checked yetcites Atagi et al., 2015
- Not checked yetcites Bailey et al., 2015
- Not checked yetcites Yeh et al., 2016 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
“Because R47H appears to be a loss-of-function mutation that impairs TREM2-mediated microglial activation (see the following sections), the study of TREM2 has been instrumental in establishing the view that microglia normally operate in a protective capacity against AD (Jay et al., 2017b; Ulrich et al., 2017; Yeh et al., 2017).”
§ Microglia in Alzheimer’s disease > Human genetic evidence for microglia involvement in late-onset AD
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“TREM2-deficient microglia showed reduced uptake of Aβ-lipoprotein complexes in vitro (Yeh et al., 2016) and less evidence of Aβ internalization in vivo (Wang et al., 2016; Yuan et al., 2016).”
§ Microglia in Alzheimer’s disease > Protective role of TREM2 and microglia in AD > Phagocytosis and clearance of Aβ and cellular debris
What the sources say
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Notably, TREM2 binds to apolipoproteins apoE and clusterin (CLU; also known as apoJ), which are themselves encoded by AD risk genes (Atagi et al., 2015; Bailey et al., 2015; Yeh et al., 2016).”
§ Microglia in Alzheimer’s disease > Protective role of TREM2 and microglia in AD
What the sources say
- Not checked yetcites Atagi et al., 2015
- Not checked yetcites Bailey et al., 2015
- Not checked yetcites Yeh et al., 2016 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“SHIP1 can interact with the phosphorylated ITAM of DAP12, so it may also moderate TREM2 signaling by competing with SYK and PI3K for ITAM occupancy (Peng et al., 2010).”
§ Microglia in Alzheimer’s disease > Potential involvement of other AD risk genes in microglial function
What the sources say
- Not checked yetcites Peng et al., 2010
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
“We suggest that the TREM2–apoE axis plays a key role in the microglial clearance of a variety of extracellular and cellular detritus and thus may be generally important for minimizing bystander damage to neurons in neurodegenerative settings.”
§ Microglia in Alzheimer’s disease > Protective role of TREM2 and microglia in AD > Phagocytosis and clearance of Aβ and cellular debris
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“The CD33 genotype–phenotype relationship nicely aligns with that of TREM2: the TREM2 R47H mutation (which increases AD risk) reduces TREM2–ligand binding and ITAM signaling and impairs phagocytosis, whereas the CD33 variant (which reduces AD risk) prevents the CD33–ligand interaction and presumably ITIM signaling and promotes phagocytosis (Bradshaw et al., 2013; Griciuc et al., 2013).”
§ Microglia in Alzheimer’s disease > Potential involvement of other AD risk genes in microglial function
What the sources say
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“the compaction of protofibrillary Aβ into a dense core plaque, which requires apoE and is promoted by TREM2 (Bales et al., 1997b, 1999; Bien-Ly et al., 2012; Wang et al., 2016; Yuan et al., 2016), could be a protective mechanism that limits neurotoxicity of amyloid deposits once they start to build up in the aging brain.”
§ Microglia in Alzheimer’s disease > Protective role of TREM2 and microglia in AD > Congregation around amyloid plaques and barrier formation
What the sources say
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“we discuss how microglia can directly mediate synapse loss (Wu et al., 2015; Spangenberg and Green, 2017) and exacerbate tau pathology (Leyns and Holtzman, 2017).”
§ Microglia in Alzheimer’s disease > Detrimental activities of microglia in AD
What the sources say
- Not checked yetcites Wu et al., 2015
- Not checked yetcites Spangenberg and Green, 2017
- Not checked yetcites Leyns and Holtzman, 2017
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Carriers of the IL1RAP polymorphism also showed reduced signal for microglial activation using a TSPO (translocator protein)-binding positron emission tomography tracer, as well as an increased rate of temporal lobe atrophy and higher likelihood of progression from mild cognitive impairment to AD.”
§ Microglia in Alzheimer’s disease > Potential involvement of other AD risk genes in microglial function
What the sources say
- Not checked yetcites Ramanan et al., 2015
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
“Collectively, the TREM2 studies suggest several mechanisms by which microglia can protect from accumulation of toxic Aβ species and development of AD: uptake and clearance of soluble Aβ species, phagocytosis of insoluble fibrillar Aβ deposits, induction of the activated state and chemotaxis, and compaction and corralling of amyloid plaques (Fig. 2).”
§ Microglia in Alzheimer’s disease > Protective role of TREM2 and microglia in AD > Congregation around amyloid plaques and barrier formation
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“TREM2-deficient microglia fail to congregate or proliferate around plaques, lack the typical morphological changes of microglial activation, and show increased apoptosis (Jay et al., 2015; Wang et al., 2015, 2016; Mazaheri et al., 2017).”
§ Microglia in Alzheimer’s disease > Protective role of TREM2 and microglia in AD > Congregation around amyloid plaques and barrier formation
What the sources say
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“electron microscopy studies have detected engulfed synaptic material in the developing hippocampus (Paolicelli et al., 2011), but not in the hippocampus of adult mice undergoing synapse loss caused by prion disease (Sisková et al., 2009; Caleo et al., 2012).”
§ Microglia in Alzheimer’s disease > Detrimental activities of microglia in AD > Microglia, complement, and synapse engulfment
What the sources say
- Not checked yetcites Paolicelli et al., 2011 source
- Not checked yetcites Sisková et al., 2009
- Not checked yetcites Caleo et al., 2012
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“Synaptic material is observed within microglia by light microscopy, and this synapse engulfment is reduced in C3 or CR3 knockout mice (Schafer et al., 2012).”
§ Microglia in Alzheimer’s disease > Detrimental activities of microglia in AD > Microglia, complement, and synapse engulfment
What the sources say
- Not checked yetcites Schafer et al., 2012 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
“INPP5D, which encodes the lipid phosphatase SHIP1, is another AD risk gene preferentially expressed in microglia.”
§ Microglia in Alzheimer’s disease > Potential involvement of other AD risk genes in microglial function
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“These protective “corralling” functions were more readily observed for small, early stage plaques and appeared compromised in mice lacking one or both copies of Trem2, as well as in human AD tissues from TREM2 R47H carriers (Condello et al., 2015; Wang et al., 2016; Yuan et al., 2016).”
§ Microglia in Alzheimer’s disease > Protective role of TREM2 and microglia in AD > Congregation around amyloid plaques and barrier formation
What the sources say
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Human microglia in aged brains or in the vicinity of tau pathology may exhibit dystrophic, fragmented morphology, further suggesting that AD develops in the context of reduced neuroprotective microglial function (Streit et al., 2004, 2009).”
§ Microglia in Alzheimer’s disease > Potential involvement of other AD risk genes in microglial function
What the sources say
- Not matchedcites Streit et al., 2004, 2009
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
None of the sources cited for this claim have been checked yet.
In the paper
“SHIP1 is involved in a clathrin-independent mode of receptor endocytosis (Boucrot et al., 2015) and inhibits phagocytosis in macrophages (Cox et al., 2001; Kamen et al., 2007).”
§ Microglia in Alzheimer’s disease > Potential involvement of other AD risk genes in microglial function
What the sources say
- Not checked yetcites Boucrot et al., 2015 source
- Not checked yetcites Cox et al., 2001
- Not checked yetcites Kamen et al., 2007
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Studies of C1q, C4, C3, and CR3 knockout mice suggest that the mechanism of developmental synapse pruning in the retinogeniculate system involves C1q tagging of synapses, opsonization of synapses by C3b, and subsequent phagocytosis of synapses by microglia (Stevens et al., 2007; Schafer et al., 2012; Sekar et al., 2016; Fig. 3 A).”
§ Microglia in Alzheimer’s disease > Detrimental activities of microglia in AD > Microglia, complement, and synapse engulfment
What the sources say
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Recent evidence suggests that microglia form a protective barrier around amyloid deposits, compacting amyloid fibrils into a tightly packed and potentially less toxic form, preventing the accretion of new Aβ onto existing plaques, and reducing axonal dystrophy in the nearby neuropil (Condello et al., 2015).”
§ Microglia in Alzheimer’s disease > Protective role of TREM2 and microglia in AD > Congregation around amyloid plaques and barrier formation
What the sources say
- Not checked yetcites Condello et al., 2015 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
“Although human genetic data argue that proper microglial function protects against AD, there is plentiful evidence that unbridled microglia activity can be harmful to neurons in neurodegenerative disease.”
§ Microglia in Alzheimer’s disease > Detrimental activities of microglia in AD
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“With β-amyloid deposition, however, some microglial processes become static, showing stable association with plaques over days or weeks, with TREM2, DAP12, and phosphotyrosine concentrated in those processes adjacent to plaques (Condello et al., 2015; Yuan et al., 2016).”
§ Microglia in Alzheimer’s disease > Protective role of TREM2 and microglia in AD > Congregation around amyloid plaques and barrier formation
What the sources say
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“The microglial gene expression profile induced by amyloid pathology (see later section on transcription) was broadly dampened in TREM2-deficient mice, indicating a key role of TREM2 in the microglial reaction to Aβ pathology (Wang et al., 2015; Keren-Shaul et al., 2017).”
§ Microglia in Alzheimer’s disease > Protective role of TREM2 and microglia in AD > Congregation around amyloid plaques and barrier formation
What the sources say
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Amyloid plaques appear a decade or two before clinical symptoms of AD, but it is tau pathology and synapse loss that correlate best with cognitive impairment during disease progression (Jack et al., 2010).”
§ Microglia in Alzheimer’s disease > Detrimental activities of microglia in AD
What the sources say
- Not checked yetcites Jack et al., 2010 source
Strength:hedged· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ 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 relationship between genotype and expression level holds true in microglia, then it might explain the elevated AD risk, because higher SHIP1 level would dampen microglial activation and phagocytosis.”
§ Microglia in Alzheimer’s disease > Potential involvement of other AD risk genes in microglial function
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- The authors state this as an assumption: The relationship between INPP5D SNP rs35349669 genotype and INPP5D expression level observed in whole blood holds true in microglia.
None of the sources cited for this claim have been checked yet.
In the paper
“Genetic knockout of C1q or neutralizing antibodies against C1q protect against synapse loss observed in amyloid-bearing mice or induced by injected Aβ (Fonseca et al., 2004; Hong et al., 2016).”
§ Microglia in Alzheimer’s disease > Detrimental activities of microglia in AD > Microglia, complement, and synapse engulfment
What the sources say
- Not checked yetcites Fonseca et al., 2004
- Not checked yetcites Hong et al., 2016 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“The PS19 study looked at 9 mo, when neurodegeneration is extensive, and observed preservation of piriform and entorhinal cortex volume in mice lacking TREM2, whereas tau phosphorylation and aggregation were unchanged (Leyns et al., 2017).”
§ Microglia in Alzheimer’s disease > Detrimental activities of microglia in AD > Microglia and tau pathology
What the sources say
- Not checked yetcites Leyns et al., 2017
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Treatment with CSF1R inhibitors to deplete microglia or disable their proliferation protects against synapse loss and rescues behavioral deficits in amyloidosis mouse models (Olmos-Alonso et al., 2016; Spangenberg et al., 2016).”
§ Microglia in Alzheimer’s disease > Detrimental activities of microglia in AD > Microglia, complement, and synapse engulfment
What the sources say
- Not checked yetcites Olmos-Alonso et al., 2016 source
- Not checked yetcites Spangenberg et al., 2016
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Recent studies of TREM2 function in mouse models of tau pathology reported seemingly conflicting roles, with Trem2 deletion appearing neuroprotective in the PS19 model (Leyns et al., 2017) but neurotoxic in the hTau model (Bemiller et al., 2017)”
§ Microglia in Alzheimer’s disease > Detrimental activities of microglia in AD > Microglia and tau pathology
What the sources say
- Not checked yetcites Leyns et al., 2017
- Not checked yetcites Bemiller et al., 2017
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
“This suggested that besides the well-known effects of apoE4 on amyloid accumulation, apoE4 may contribute to AD pathogenesis by exacerbating neuroinflammation and tau pathology.”
§ Microglia in Alzheimer’s disease > Detrimental activities of microglia in AD > Microglia and tau pathology
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“this was reportedly accompanied by increased proinflammatory cytokines, tau pathology, and functional deficits (Cho et al., 2011; Lee et al., 2014).”
§ Microglia in Alzheimer’s disease > Detrimental activities of microglia in AD > Microglia and tau pathology
What the sources say
- Not checked yetcites Cho et al., 2011
- Not checked yetcites Lee et al., 2014 source
Strength:hedged· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“Mouse models of β-amyloidosis exhibit elevated C1q levels, with increased synaptic localization of C1q even before plaques have formed (Hong et al., 2016).”
§ Microglia in Alzheimer’s disease > Detrimental activities of microglia in AD > Microglia, complement, and synapse engulfment
What the sources say
- Not checked yetcites Hong et al., 2016 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
“Thus, although there are conflicting results, most published studies in amyloidosis mouse models suggest that depleting microglia and blocking complement pathway activation may have beneficial effects in AD, at least in terms of synapse and neuron loss (Fig. 3 B).”
§ Microglia in Alzheimer’s disease > Detrimental activities of microglia in AD > Microglia, complement, and synapse engulfment
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“C1q is expressed in the adult brain, and protein levels rise steeply with aging, especially in the hippocampus (Stephan et al., 2013).”
§ Microglia in Alzheimer’s disease > Detrimental activities of microglia in AD > Microglia, complement, and synapse engulfment
What the sources say
- Not checked yetcites Stephan et al., 2013 source
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“AD-associated genes include CR1 (complement receptor 1), which plays roles in phagocytosis, clearing of immune complexes, and inhibition of complement (Khera and Das, 2009; Fonseca et al., 2016), and CLU/apoJ, which reportedly can function as an inhibitor of the terminal complement complex (Murphy et al., 1989; Tschopp et al., 1993; McDonald and Nelsestuen, 1997).”
§ Microglia in Alzheimer’s disease > Detrimental activities of microglia in AD > Microglia, complement, and synapse engulfment
What the sources say
- Not checked yetcites Khera and Das, 2009
- Not checked yetcites Fonseca et al., 2016 source
- Not checked yetcites Murphy et al., 1989
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
“Overall, the findings imply that synapse loss around plaques is dynamically regulated by microglia and can be potentially rescued by microglia depletion despite no change or possible increase in amyloid plaque size.”
§ Microglia in Alzheimer’s disease > Detrimental activities of microglia in AD > Microglia, complement, and synapse engulfment
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“β-Amyloid aggregates/fibrils can act as disease-associated molecular patterns and stimulate Toll-like receptors (TLRs) and the NRLP3 inflammasome (Heneka et al., 2013, 2015), resulting in microglial production of TNFα, IL-1β, and other inflammatory cytokines.”
§ Microglia in Alzheimer’s disease > Detrimental activities of microglia in AD > Microglia and neurotoxic inflammatory signaling
What the sources say
- Not matchedcites Heneka et al., 2013, 2015
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
“The study in the hTau model looked at 6 mo (long before neuronal loss) and observed greater tau phosphorylation and aggregation in TREM2-deficient mice, arguing for an early protective role of TREM2 in restraining propagation of tauopathy (Bemiller et al., 2017).”
§ Microglia in Alzheimer’s disease > Detrimental activities of microglia in AD > Microglia and tau pathology
What the sources say
- Not checked yetcites Bemiller et al., 2017
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“These studies point to a disease-associated microglial (DAM) state in which expression of a “homeostatic” gene set is reduced (e.g., Cx3cr1, P2ry12, and Tmem119) and another set of “neurodegeneration” genes is highly induced (e.g., Apoe, Axl, Csf1, Clec7a, Cst7, Igf1, Itgax/CD11c, Lilrb4, Lpl, and some major histocompatibility complex class II genes).”
§ Microglia in Alzheimer’s disease > Microglial activation states defined by transcriptional profiling
What the sources say
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“RNA-sequencing studies of human microglia isolated from non-AD brain tissue (Galatro et al., 2017; Gosselin et al., 2017) showed broad similarity with mouse microglial gene expression profiles, although there were many differences such as higher expression of the C2 and C3 complement genes in human microglia.”
§ Microglia in Alzheimer’s disease > Microglial activation states defined by transcriptional profiling
What the sources say
- Not checked yetcites Galatro et al., 2017
- Not checked yetcites Gosselin et al., 2017 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
“Notably, DAM cells increase in number with progression of amyloidosis, lie spatially close to amyloid plaque, and show evidence of Aβ uptake.”
§ Microglia in Alzheimer’s disease > Microglial activation states defined by transcriptional profiling
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.
The paper relies on this without support.
Soluble oligomeric Aβ is the form that exerts the most toxic effects on neurons.
“A halo of soluble, oligomeric Aβ (the form currently thought to exert the most toxic effects on neurons) likely exists around amyloid plaques.”
The authors state this as an assumption.
The relationship between INPP5D SNP rs35349669 genotype and INPP5D expression level observed in whole blood holds true in microglia.
“If this relationship between genotype and expression level holds true in microglia, then it might explain the elevated AD risk, because higher SHIP1 level would dampen microglial activation and phagocytosis.”
The paper relies on this without support.
Microglia express the C3a and C5a receptors that trigger inflammation in response to complement activation.
“and they express the C3a and C5a receptors that trigger inflammation in response to complement activation.”
The paper relies on this without support.
Findings in amyloidosis and tauopathy mouse models are informative about the mechanisms of microglial function in human AD.
“most published studies in amyloidosis mouse models suggest that depleting microglia and blocking complement pathway activation may have beneficial effects in AD, at least in terms of synapse and neuron loss”
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 source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Activated microglia and astrocytes can phagocytize Aβ through multiple receptors to protect neurons,33,34 but failure to clear the aggregates leads to persistent chronic inflammation and the release of a variety of proinflammatory and toxic products, including cytokines, chemokines, reactive oxygen species (ROS) and nitric oxide (NO), which amplify immune responses and lead to neurotoxicity.35”
From Role of neuroinflammation in neurodegeneration development (2023) · cites this paper as [35]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Especially, the interaction of microglia within the complex brain microenvironment of AD (e.g. neurons, astrocytes and amyloid-β plaques) is still not well explored.11, 12”
From Acoustofluidic assembly of 3D neurospheroids to model Alzheimer's disease (2020) · cites this paper as [12]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“In the brain, PLCγ2 is primarily expressed by microglia, where it serves as an important signaling node downstream of TREM2 and CD33 (19, 20), both also AD risk genes (21–23).”
From Multi-omics analyses reveal novel effects of PLCγ2 deficiency in the mouse brain (2023) · cites this paper as [20]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Within the brain, PLCγ2 is primarily but not exclusively expressed in microglia, where it serves as an important signaling node downstream of TREM2 and CD33 [31, 32], both also AD risk genes [33–35].”
From PLCγ2 deficiency compromises systemic immune tolerance and erodes myelin homeostasis while enhancing oxidative metabolism in the mouse brain (2026) · cites this paper as [32]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Conversely, extensive microglial activation promotes chronic neuroinflammation, which causes neuronal damage and thus is a major player in AD pathogenesis alongside β-amyloid aggregation and hyperphosphorylated tau deposition [4].”
From The protective PLCγ2-P522R variant mitigates Alzheimer’s disease-associated pathologies by enhancing beneficial microglial functions (2025) · cites this paper as [4]
Experimental — accuracy not yet measured
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“APOE ε4 is known to disrupt lipid homeostasis and immune response and to cause mitochondrial dysfunction [31–34]”
From Protective PLCG2 variants associate with a delayed onset of Alzheimer’s disease among heterozygous APOE ε4 carriers (2026) · cites this paper as [31]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Transcriptionally, the DAM signature includes downregulation of genes expressed in homeostatic microglia such as CX3CR1 and P2RY12 and upregulation of genes including APOE, AXL, SPP1 and TREM2, as well as major histocompatibility complex class II (MHC-II), a gene essential for the initiation of antigen-specific immune response [27–29].”
From Microglial function, INPP5D/SHIP1 signaling, and NLRP3 inflammasome activation: implications for Alzheimer’s disease (2023) · cites this paper as [29]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Likewise, microglia, the brain-resident immunocompetent macrophages, also recognize Aβ oligomers via receptors such as CD36, toll-like receptor 4 (TLR4) and TLR6 and triggering receptor expressed on myeloid cells 2 (TREM2), acquiring specific AD-associated phenotypes [14,15,16].”
From Emerging Role of miR-21-5p in Neuron–Glia Dysregulation and Exosome Transfer Using Multiple Models of Alzheimer’s Disease (2022) · cites this paper as [16]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“In addition, several studies showed the paramount role of microglial cells in maintaining tissue homeostasis and keeping the extracellular space clean of β-amyloid (Aβ), thereby preventing AD [27].”
From Oral Microbially-Induced Small Extracellular Vesicles Cross the Blood–Brain Barrier (2024) · cites this paper as [27]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Besides neurons, glia and in particular microglia are now considered a second brain cell type phenotypic of AD’s cellular pathologies (Salter and Stevens, 2017; Hansen et al., 2018; Takatori et al., 2019; Streit et al., 2020), which play a dominant role in modulating how the brain responds to AD’s triggering neuronal-based pathologies.”
From The neuronal retromer can regulate both neuronal and microglial phenotypes of Alzheimer's disease (2022) · cites this paper as Hansen et al., 2018
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“The microglial response to amyloid plaques in AD can range from neuroprotective to neurotoxic2.”
From Lymphoid gene expression supports neuroprotective microglia function (2025) · cites this paper as [2]
The cited source says what the claim attributes to it.
In the citing paper
“Human genetic studies suggest that reduced SPI1 expression may be protective, whereas experimental data indicate that excessive PU.1 suppression can impair essential microglial functions.”
From Lymphoid-like Suppressive Microglia in Alzheimer’s Disease: A New Neuroimmune Regulatory Axis? (2026) · cites this paper as [12]
The cited source says what the claim attributes to it.
In the citing paper
“in disease, these same capacities can become either protective or damaging depending on context, timing, and molecular state [10,11,12].”
From Lymphoid-like Suppressive Microglia in Alzheimer’s Disease: A New Neuroimmune Regulatory Axis? (2026) · cites this paper as [12]
The cited source says what the claim attributes to it.
In the citing paper
“This older binary language is now considered too limited.”
From Lymphoid-like Suppressive Microglia in Alzheimer’s Disease: A New Neuroimmune Regulatory Axis? (2026) · cites this paper as [12]
The cited source says what the claim attributes to it.
In the citing paper
“The key implication was that Alzheimer’s risk could be influenced not only by coding changes in immune genes, but also by regulatory variants that alter how strongly a myeloid transcription factor is expressed.”
From Lymphoid-like Suppressive Microglia in Alzheimer’s Disease: A New Neuroimmune Regulatory Axis? (2026) · cites this paper as [12]
The cited source says what the claim attributes to it.
In the citing paper
“A common protective haplotype associated with lower SPI1 expression was reported to delay Alzheimer’s disease onset, suggesting that reduced PU.1 abundance in myeloid cells may be beneficial under some disease-relevant conditions.”
From Lymphoid-like Suppressive Microglia in Alzheimer’s Disease: A New Neuroimmune Regulatory Axis? (2026) · cites this paper as [12]
The cited source says what the claim attributes to it.
In the citing paper
“Although microglia are heavily implicated in the pathogenesis of AD [118]”
From TREM2/PLCγ2 signalling in immune cells: function, structural insight, and potential therapeutic modulation (2021) · cites this paper as [118]
The cited source says what the claim attributes to it.
In the citing paper
“Microglial cells represent the main innate immune population residing in the central nervous system (CNS). Through the clearance of pathogens, dead cells, and protein aggregates such as A β , they play a critical role in CNS immune surveillance and the preservation of tissue homeostasis [33,34].”
From Is there a role for B cells in Alzheimer's disease? (2026) · cites this paper as [34]
The cited source says what the claim attributes to it.
In the citing paper
“microglia dysfunction has also been suspected to be involved in AD through modulating Aβ aggregation/degradation [45].”
From The new genetic landscape of Alzheimer’s disease: from amyloid cascade to genetically driven synaptic failure hypothesis? (2019) · cites this paper as [45]
In the citing paper
“Microglia are increasingly recognized as a central cell type contributing to the etiology of AD32.”
From A computational tool (H-MAGMA) for improved prediction of brain-disorder risk genes by incorporating brain chromatin interaction profiles (2020) · cites this paper as [32]
In the citing paper
“Inappropriate control of the classical complement cascade causes unresolvable inflammation and disease (Hong et al. , 2016; Hansen, Hanson and Sheng, 2018; Morgan, 2018).”
From Spatial Transcriptomics and In Situ Sequencing to Study Alzheimer’s Disease (2020) · cites this paper as Hansen, Hanson and Sheng, 2018
In the citing paper
“genetic and histological findings suggest that human AD involves impairments in microglial activation (Hansen et al., 2018; Streit et al., 2009).”
From Alzheimer’s Patient Microglia Exhibit Enhanced Aging and Unique Transcriptional Activation (2020) · cites this paper as Hansen et al., 2018
In the citing paper
“In neurodegenerative state, microglia can enhance neuroinflammation leading to more cell deaths [6, 8].”
From Transcriptional and Epigenetic Regulation of Microglia in Health and Disease (2019) · cites this paper as [8]
In the citing paper
“Importantly, the capability of astrocytes and microglia to internalize and degrade Aβ (Guénette, 2003; Hansen et al., 2018) is strictly correlated with their aberrant activation during the AD progression (Bates et al., 2009; Ries and Sastre, 2016).”
From Exploring the Therapeutic Potential of Phytochemicals in Alzheimer’s Disease: Focus on Polyphenols and Monoterpenes (2022) · cites this paper as Hansen et al., 2018
In the citing paper
“However, in a reactionary or dystrophic state, microglia also contribute to the pathogenesis of various NDs and post-TBI syndromes [43–45].”
From Untangling senescent and damage‐associated microglia in the aging and diseased brain (2023) · cites this paper as [43]
In the citing paper
“Discoveries over the last decade suggest that many, perhaps even a majority, of the genes contributing risk to AD are expressed primarily by microglia (1, 2), the resident myeloid cells of the brain parenchyma.”
From The Transcriptional Landscape of Microglial Genes in Aging and Neurodegenerative Disease (2019) · cites this paper as [2]
Citations
Cites
1 retracted
Microglia-dependent synapse loss in type I interferon-mediated lupus
Bialas, A. R., Presumey, J., Das, A., van der Poel, C. E., Lapchak, P. H., Mesin, L., Victora, G., Tsokos, G. C., Mawrin, C., Herbst, R., et al. (2017) · Nature · doi:10.1038/nature22821 · Cited by 197 · cited 2×
“…molecules in the brain, is present in Aβ plaques (Namba et al., 1991; Wisniewski and Frangione, 1992; Zhan et al., 1995) and contributes to both the clearance and the amyloid deposition of Aβ peptide (Bales et al., 1997a; DeMattos et al., 2004; Bien-Ly et al., 2012; Holtzman et al., 2012).”
BackgroundRetractedAmyloid oligomers exacerbate tau pathology in a mouse model of tauopathy
Selenica, M.-L. B., Brownlow, M., Jimenez, J. P., Lee, D. C., Pena, G., Dickey, C. A., Gordon, M. N., & Morgan, D. (2013) · Neurodegenerative Diseases · doi:10.1159/000337230 · Cited by 10,359
Corder, E. H., Saunders, A. M., Strittmatter, W. J., Schmechel, D. E., Gaskell, P. C., Small, G. W., Roses, A. D., Haines, J. L., & Pericak-Vance, M. A. (1993) · Science · doi:10.1126/science.8346443 · Cited by 9,429
Neurotoxic reactive astrocytes are induced by activated microglia
Liddelow, S. A., Guttenplan, K. A., Clarke, L. E., Bennett, F. C., Bohlen, C. J., Schirmer, L., Bennett, M. L., Münch, A. E., Chung, W.-S., Peterson, T. C., et al. (2017) · Nature · doi:10.1038/nature21029 · Cited by 7,971
The amyloid hypothesis of Alzheimer's disease at 25 years
Selkoe, D. J., & Hardy, J. (2016) · EMBO Molecular Medicine · doi:10.15252/emmm.201606210 · Cited by 6,164 · cited 1×
“Knockout or inhibition of C3, which should block all pathways of complement activation, is also reported to provide neuroprotection (Shi et al., 2015, 2017a; Hong et al., 2016; for different results, see Wyss-Coray et al., 2002; Maier et al., 2008), though it appears to increase amyloid burden…”
BackgroundResting microglial cells are highly dynamic surveillants of brain parenchyma in vivo
Nimmerjahn, A., Kirchhoff, F., & Helmchen, F. (2005) · Science · doi:10.1126/science.1110647 · Cited by 5,827 · cited 1×
“Involved in chemotactic polarization and migration of macrophages (Okigaki et al., 2003).”
BackgroundA Unique Microglia Type Associated with Restricting Development of Alzheimer’s Disease
Keren-Shaul, H., Spinrad, A., Weiner, A., Matcovitch-Natan, O., Dvir-Szternfeld, R., Ulland, T. K., David, E., Baruch, K., Lara-Astaiso, D., Toth, B., et al. (2017) · Cell · doi:10.1016/j.cell.2017.05.018 · Cited by 5,493 · cited 6×
“Analyzing activated microglia as a separate population or by single-cell RNA-sequencing also reveals subtle (two- to threefold) increases in Trem2 and Tyrobp mRNAs (Kamphuis et al., 2016; Keren-Shaul et al., 2017; Yin et al., 2017).”
BackgroundMethodInfluentialFate Mapping Analysis Reveals That Adult Microglia Derive from Primitive Macrophages
Ginhoux, F., Greter, M., Leboeuf, M., Nandi, S., See, P., Gokhan, S., Mehler, M. F., Conway, S. J., Ng, L. G., Stanley, E. R., et al. (2010) · Science · doi:10.1126/science.1194637 · Cited by 5,175 · cited 1×
“Their homeostasis and self-renewal is maintained by several factors, including TGF-β and CSF1R signaling (Ginhoux et al., 2010; Butovsky et al., 2014; Elmore et al., 2014).”
BackgroundHypothetical model of dynamic biomarkers of the Alzheimer's pathological cascade
Jack, C. R., Knopman, D. S., Jagust, W. J., Shaw, L. M., Aisen, P. S., Weiner, M. W., Petersen, R. C., & Trojanowski, J. Q. (2010) · The Lancet Neurology · doi:10.1016/s1474-4422(09)70299-6 · Cited by 4,806 · cited 1×
“Amyloid plaques appear a decade or two before clinical symptoms of AD, but it is tau pathology and synapse loss that correlate best with cognitive impairment during disease progression (Jack et al., 2010).”
BackgroundComplement factor H polymorphism in age-related macular degeneration
Klein, R. J., Zeiss, C., Chew, E. Y., Tsai, J.-Y., Sackler, R. S., Haynes, C., Henning, A. K., SanGiovanni, J. P., Mane, S. M., Mayne, S. T., et al. (2005) · Science · doi:10.1126/science.1109557 · Cited by 4,492
Flagged first, then by citations
Research works printed but not linked: 1
- Bales, 1997, Lack of apolipoprotein E dramatically reduces amyloid beta-peptide deposition, Nat. Genet., 17, 263, 10.1038/ng1197-263 · DOI · Paper page
Cited by
Sorted by citations
Items 501–600 of 1,017
Mo, Y., Deng, S., Zhang, L., Huang, Y., Li, W., Peng, Q., Liu, Z., & Ai, Y. (2019) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2019.09.077 · Cited by 35
Avallone, R., Lucchi, C., Puja, G., Codeluppi, A., Filaferro, M., Vitale, G., Rustichelli, C., & Biagini, G. (2020) · Cells · doi:10.3390/cells9092091 · Cited by 36
“In neurological diseases such as Parkinson’s disease (PD) [13], Alzheimer’s disease (AD) [14,15] and multiple sclerosis (MS) [16], microglia are rapidly activated to acquire a M1 phenotype [17].”
BackgroundCory‐Slechta, D. A., Sobolewski, M., & Oberdörster, G. (2020) · Atmosphere · doi:10.3390/atmos11101098 · Cited by 36
Enjoy Carefully: The Multifaceted Role of Vitamin E in Neuro-Nutrition
Regner-Nelke, L., Nelke, C., Schroeter, C. B., Dziewas, R., Warnecke, T., Ruck, T., & Meuth, S. G. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms221810087 · Cited by 36
“However, microglia activation may be protective in the early stages of AD, as microglia clear soluble Aβ, build protective barriers around Aβ plaques and remove debris [105,106].”
BackgroundMontalbano, M., Majmundar, L., Sengupta, U., Fung, L., & Kayed, R. (2022) · Brain Pathology · doi:10.1111/bpa.13112 · Cited by 35
Khan, K. M., Balasubramanian, N., Gaudencio, G., Wang, R., Selvakumar, G. P., Kolling, L. J., Pierson, S. R., Tadinada, S. M., Abel, T. G., Hefti, M. M., et al. (2023) · Acta Neuropathologica Communications · doi:10.1186/s40478-023-01546-5 · Cited by 37
“Pro-inflammatory cytokines like IL-1β activate local microglia and astrocytes that respond by releasing more cytokines and other signaling molecules, including glutamate, which can impact neuronal function and survival [51, 53, 89].”
BackgroundGene networks and systems biology in Alzheimer's disease: Insights from multi‐omics approaches
Rahimzadeh, N., Srinivasan, S. S., Zhang, J., & Swarup, V. (2024) · Alzheimer s & Dementia · doi:10.1002/alz.13790 · Cited by 39
“20 Following this ideation, isolation of single cells and celltypesallowforunderstandingspecificcelltyperesponsesandreac-tions to AD pathology.”
BackgroundZhang, S.-S., Gao, Z., Feng, L., & Li, M. (2024) · Journal of Inflammation Research · doi:10.2147/jir.s483412 · Cited by 39
Yao, M., Wei, Z., Nielsen, J. S., Ouyang, Y., Kakazu, A., Wang, H., Du, L., Li, R., Chu, T., Scafidi, S., et al. (2024) · Neurobiology of Disease · doi:10.1016/j.nbd.2024.106711 · Cited by 38
“…the advancement of senolytic therapies with higher efficacy and reduced side effects to clinical application. f Recent studies show that most genetic risk variants associated with late-onset AD are present in microglia, indicating that microglia may play a causal role in the disease (17-19).”
Amyloid Proteins and Peripheral Neuropathy
Albariqi, M. M. H., Engelsman, S., Eijkelkamp, N., & Höppener, J. W. M. (2020) · Cells · doi:10.3390/cells9061553 · Cited by 41
García‐León, J. A., Cáceres-Palomo, L., Sánchez‐Mejías, E., Mejias‐Ortega, M., Nuñez‐Diaz, C., Fernandez-Valenzuela, J. J., Sanchez-Varo, R. M., Dávila, J. C., Vitórica, J., & Gutiérrez, A. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21186867 · Cited by 35
“Therefore, there are conflicting reports as it seems that microglia response in AD may play a dual role, being either beneficial or harmful [12,13], although this fact most probably will respond to differences in models used, brain regions, and/or disease stage examined.”
BackgroundChen, X., Chen, D., Li, Q., Wu, S., Pan, J., Liao, Y., Zheng, X., & Zeng, W. (2021) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2021/6643171 · Cited by 35
“An increasing number of studies have revealed that dexmedetomidine exhibits neuroprotective activities in numerous neurological disorders, including Alzheimer’s disease, traumatic brain injury (TBI), and cerebral ischemia [24–26].”
BackgroundMicroglia and modifiable life factors: Potential contributions to cognitive resilience in aging
Duggan, M. R., & Parikh, V. (2021) · Behavioural Brain Research · doi:10.1016/j.bbr.2021.113207 · Cited by 38
Song, X., Cui, Z., He, J., Yang, T., & Sun, X. (2021) · Molecular Medicine Reports · doi:10.3892/mmr.2021.12168 · Cited by 35
New insights in drug development for Alzheimer's disease based on microglia function
Qiao, O., Ji, H., Zhang, Y., Zhang, X., Zhang, X., Liu, N., Huang, L., Liu, C., & Gao, W. (2021) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2021.111703 · Cited by 35
Wang, Q., Davis, P. B., Qi, X., Chen, S. G., Gurney, M. E., Perry, G. L., Doraiswamy, P. M., & Xu, R. (2021) · Alzheimer s Research & Therapy · doi:10.1186/s13195-021-00917-1 · Cited by 35
Althafar, Z. M. (2022) · Molecules · doi:10.3390/molecules27134124 · Cited by 36
Gado, F., Ferrisi, R., Polini, B., Mohamed, K. A., Ricardi, C., Lucarini, E., Carpi, S., Domenichini, F., Stevenson, L., Rapposelli, S., et al. (2022) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.2c00582 · Cited by 35
You, S., Su, X., Ying, J., Li, S., Qu, Y., & Mu, D. (2022) · Biomolecules · doi:10.3390/biom12081158 · Cited by 35
“Moreover, excessive Aβ levels disrupt the balance between microglial phagocytosis and Aβ production [95].”
BackgroundBorbély, E., Varga, V. É., Szögi, T., Schuster, I., Bozsó, Z., Penke, B., & Fülöp, L. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23052514 · Cited by 35
Chen, R., Routh, B. N., Straetker, J. E., Gibson, C. R., Weitzner, A. S., Bell, K. S., Gaudet, A. D., & Fonken, L. K. (2023) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2023.08.029 · Cited by 34
Nutraceutical and therapeutic potential of Phycocyanobilin for treating Alzheimer’s disease
Piniella‐Matamoros, B., Marín‐Prida, J., & Pentón‐Rol, G. (2021) · Journal of Biosciences · doi:10.1007/s12038-021-00161-7 · Cited by 34
Wan, T., Fu, M., Jiang, Y., Jiang, W., Li, P., & Zhou, S. (2021) · Neurochemical Research · doi:10.1007/s11064-021-03448-1 · Cited by 38
Li, S., Xiao, J., Huang, C., & Sun, J. (2023) · Scientific Reports · doi:10.1038/s41598-023-27977-7 · Cited by 35
Anti-Neuroinflammatory Potential of Natural Products in the Treatment of Alzheimer’s Disease
Deng, M., Yan, W., Gu, Z., Li, Y., Chen, L., & He, B. (2023) · Molecules · doi:10.3390/molecules28031486 · Cited by 38
“Under normal physiological conditions, microglia are rapidly switched from the M1 phenotype to the M2 phenotype and then secrete the appropriate nutritional and anti-inflammatory factors including brain-derived neurotrophic factor (BDNF), nerve growth factor (NGF) and interleukin-1 (IL-1) to terminate the immune respo…”
BackgroundKopeć, K., Szleszkowski, S., Koziorowski, D., & Szlufik, S. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241210366 · Cited by 36
Rh‐CSF1 attenuates neuroinflammation via the CSF1R/PLCG2/PKCε pathway in a rat model of neonatal HIE
Hu, X., Li, S., Doycheva, D. M., Huang, L., Lenahan, C., Liu, R., Huang, J., Xie, S., Tang, J., Zuo, G., et al. (2020) · Journal of Neuroinflammation · doi:10.1186/s12974-020-01862-w · Cited by 35
Zhu, X., Huang, J., Wu, Y., Zhao, S., & Chai, X. (2021) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-021-01165-5 · Cited by 34
“But the chronically activated microglia in neurodegenerative diseases could exacerbate the condition by releasing too much of cytotoxic factors like Alzheimer’s disease (Hansen et al. 2018), Parkinson’s disease (Pajares et al.”
BackgroundLiu, Y., Tan, Y., Zhang, Z., Li, H., Yi, M., Zhang, Z., Hui, S., & Peng, W. (2022) · Ageing Research Reviews · doi:10.1016/j.arr.2022.101831 · Cited by 34
Senescent Microglia Represent a Subset of Disease-Associated Microglia in P301S Mice
Ng, P. Y., Zhang, C., Li, H., & Baker, D. J. (2023) · Journal of Alzheimer s Disease · doi:10.3233/jad-230109 · Cited by 38
“However, with the key role that microglia play in neurodegenerative disease [24, 25], defining the presence of senescent microglia and their differences from non-senescent inflammatory microglia remains an important point to address.”
Hickey, J. P., Collins, A. E., Nelson, M. L., Chen, H., & Kalisch, B. E. (2024) · Current Issues in Molecular Biology · doi:10.3390/cimb46050266 · Cited by 39
Sanfilippo, C., Castrogiovanni, P., Imbesi, R., Tibullo, D., Volti, G. L., Barbagallo, I. A., Vicario, N., Musumeci, G., & Rosa, M. D. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2019.03.008 · Cited by 31
Human brain development through the lens of cerebral organoid models
Andrews, M. G., & Nowakowski, T. J. (2019) · Brain Research · doi:10.1016/j.brainres.2019.146470 · Cited by 35
“Dysregulation of microglia in the aged brain is implicated in many neurodegenerative diseases, including Alzheimer’s and Parkinson’s disease (Hansen et al., 2018; Keren-Shaul et al., 2017; Liu et al., 2019), and without these cells these diseases cannot be accurately modeled.”
BackgroundFernández‐Mendívil, C., Arreola, M. A., Hohsfield, L. A., Green, K. N., & López, M. G. (2020) · Antioxidants · doi:10.3390/antiox9070644 · Cited by 33
“We have focused on microglia for several reasons: (i) microglia, the innate immune cells of the CNS, are considered the first line of defense against pathogens or cell damage [10,12,31], (ii) low-grade neuroinflammation is recognized as a hallmark in the pathology of AD and other NDDs [12], (ii) previous reports, indi…”
BackgroundFreeman, J. L., & Kiper, K. (2021) · Current Neuropharmacology · doi:10.2174/1570159x19666210524155944 · Cited by 33
The role of mitochondrial genome abundance in Alzheimer's disease
Harerimana, N. V., Paliwali, D., Romero‐Molina, C., Bennett, D. A., Pa, J., Goate, A., Swerdlow, R. H., & Andrews, S. J. (2022) · Alzheimer s & Dementia · doi:10.1002/alz.12812 · Cited by 32
“When Ab levels accumulate beyond their clearing ability, microglia compact Ab aggregates into less toxic dense core neuritic plaques [39].”
BackgroundMicroglia and Cholesterol Handling: Implications for Alzheimer’s Disease
Herrera, O. M. M., & Zivkovic, A. M. (2022) · Biomedicines · doi:10.3390/biomedicines10123105 · Cited by 38
Alzheimer’s Disease and Protein Kinases
Engin, A. B., & Engin, A. (2021) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-49844-3_11 · Cited by 43
Yuan, S., Wu, W., Ma, W., Huang, X., Huang, T., Peng, M., Xu, A., & Lyu, J. (2022) · Journal of Translational Medicine · doi:10.1186/s12967-022-03621-2 · Cited by 32
“In addition, microglia are innate immune cells of the central nervous system, which can prevent development of AD by inhibiting accumulation of Aβ [51].”
Liu, X., Cheng, Z.-Y., Li, Y.-F., Liu, C., Wang, C., Gong, X., & He, L. (2022) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2022.175443 · Cited by 32
Boraschi, D., Italiani, P., Migliorini, P., & Bossù, P. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1128190 · Cited by 38
Papadopoulou, P., Polissidis, A., Kythreoti, G., Sagnou, M., Stefanatou, A., & Theoharides, T. C. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252011040 · Cited by 36
The microglial translocator protein (TSPO) in Alzheimer’s disease reflects a phagocytic phenotype
Garland, E. F., Antony, H., Kulagowska, L., Scott, T., Rogien, C., Bottlaender, M., Nicoll, J. A. R., & Boche, D. (2024) · Acta Neuropathologica · doi:10.1007/s00401-024-02822-x · Cited by 31
“Finally, there is literature to suggest that both may occur in AD [17].”
Chen, W., Liu, X., Muñoz, V. R., & Kahn, C. R. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2501527122 · Cited by 42
“In AD, it is known that the deposition of A β triggers activation of glial cells, including astrocytes and microglia, which initially try to protect against this process ( 48 ).”
Dual impact of neuroinflammation on cognitive and motor impairments in Alzheimer's disease
Fakorede, S., Lateef, O. M., Garuba, W. A., Akosile, P. O., Okon, D. A., & Aborode, A. T. (2025) · Journal of Alzheimer s Disease Reports · doi:10.1177/25424823251341870 · Cited by 40
“32 – 34 Microglia exist in a continuum of activation states, rather than the traditionally de fi ned M1 (pro-in fl ammatory, neuro-toxic) and M2 (anti-in fl ammatory, neuroprotective) dichotomy.”
Epigenetic clocks and DNA methylation biomarkers of brain health and disease
Conole, E. L. S., Robertson, J. A., Smith, H. M., Cox, S. R., & Marioni, R. E. (2025) · Nature Reviews Neurology · doi:10.1038/s41582-025-01105-7 · Cited by 38
“Bulk DNAm profiling might obscure disease-specific alterations in brain cell types 26 , particularly in the context of Alzheimer disease, which is characterized by changes in the activation, proliferation and proportions of distinct cell populations 27 .”
Unravelling the glial response in the pathogenesis of Alzheimer's disease
Alibhai, J. D., Diack, A. B., & Manson, J. C. (2018) · The FASEB Journal · doi:10.1096/fj.201801360r · Cited by 31
“A significant proportion of genes identified in genome-wide association studies as being associated with risk for sporadic AD are involved in microglial functions [reviewed elsewhere (79)].”
BackgroundTherapeutic Potential of Wnt-3a in Neurological Recovery after Spinal Cord Injury
Gao, K., Zhang, T., Wang, F., & Lv, C. (2019) · European Neurology · doi:10.1159/000502004 · Cited by 32
Ano, Y., Kita, M., Kitaoka, S., & Furuyashiki, T. (2019) · Nutrients · doi:10.3390/nu11092161 · Cited by 33
West Nile Virus-Induced Neurologic Sequelae—Relationship to Neurodegenerative Cascades and Dementias
Vittor, A. Y., Long, M. T., Chakrabarty, P., Aycock, L., Kollu, V., & DeKosky, S. T. (2020) · Current Tropical Medicine Reports · doi:10.1007/s40475-020-00200-7 · Cited by 32
Wu, K.-Y., Tang, F., Lee, D., Zhao, Y., Song, H., Zhu, X., Mei, L., & Xiong, W. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.1520-19.2020 · Cited by 33
Sohrabi, M., Pecoraro, H. L., & Combs, C. K. (2021) · Journal of Alzheimer s Disease · doi:10.3233/jad-201099 · Cited by 31
“Impaired microglial phagocytosis activity in response to A (cid:2) plaque deposition plays a hypothesized role in pathogenesis and progression of AD [5, 6, 91–93].”
Xue, F., Tian, J., Yu, C., Du, H., & Guo, L. (2021) · Neurobiology of Disease · doi:10.1016/j.nbd.2021.105272 · Cited by 32
The Specific Mechanism of TREM2 Regulation of Synaptic Clearance in Alzheimer’s Disease
Qin, Q., Wang, M., Yin, Y., & Tang, Y. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.845897 · Cited by 34
“However, excessive Ab oligomers can stimulate the complement cascade pathway and induce microglia to excessively phagocytose and clear synapses in a manner similar to normal synaptic pruning, resulting in synaptic loss in AD patients (13).”
BackgroundQin, Y., Ma, C., Jiang, J., Wang, D., Zhang, Q., Liu, M., Zhao, H., Fang, Q., & Liu, Y. (2022) · Journal of Neurochemistry · doi:10.1111/jnc.15620 · Cited by 33
Particulate matter and Alzheimer’s disease: an intimate connection
O’Piela, D. R., Durisek, G., Escobar, Y.-N. H., Mackos, A. R., & Wold, L. E. (2022) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2022.06.004 · Cited by 36
Advances in fucoxanthin chemistry and management of neurodegenerative diseases
Li, N., Gao, X., Zheng, L., Huang, Q., Zeng, F., Chen, H., Farag, M. A., & Zhao, C. (2022) · Phytomedicine · doi:10.1016/j.phymed.2022.154352 · Cited by 34
Brain Fog: a Narrative Review of the Most Common Mysterious Cognitive Disorder in COVID-19
Mir, M. A. (2023) · Molecular Neurobiology · doi:10.1007/s12035-023-03715-y · Cited by 38
“Moreover, it has been claimed that the NLRP3 inflammasome is much safer than other NRF2 electrophilic activators because it is inhibited by CA. CA also suppresses cytokine storm and inhibits microglia [144–147].”
The neuronal retromer can regulate both neuronal and microglial phenotypes of Alzheimer's disease
Qureshi, Y. H., Berman, D. E., Marsh, S. E., Klein, R. L., Patel, V. M., Simoes, S., Kannan, S., Petsko, G. A., Stevens, B., & Small, S. A. (2022) · Cell Reports · doi:10.1016/j.celrep.2021.110262 · Cited by 31
Gao, S., Jia, S., Bai, L., Li, D., & Meng, C. (2022) · Cells · doi:10.3390/cells11243956 · Cited by 32
“There is consensus that microglia are significantly associated with Alzheimer’s disease [5], Parkinson’s disease [6], and amyotrophic lateral sclerosis [7].”
BackgroundSighencea, M. G., Popescu, R. Ș., & Trifu, S. C. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252212311 · Cited by 33
“Inflammatory mediators related to periodontal disease, including cytokines IL-1 β , IL-6, and TNF α , have also been suggested to promote neuroinflammation, accelerating AD progression [282,283].”
Onisiforou, A., Charalambous, E. G., & Zanos, P. (2025) · Microorganisms · doi:10.3390/microorganisms13010090 · Cited by 32
“Microglia, which are critical to AD development, play a key role in engulfing and clearing apoptotic neurons, bacteria, lipoproteins, and A β [68].”
Bellelli, F., Angioni, D., Arosio, B., Vellas, B. J., & Barreto, P. D. S. (2025) · Ageing Research Reviews · doi:10.1016/j.arr.2025.102699 · Cited by 34
Zhao, W., Liu, Z., Wu, J., Liu, A., & Yan, J. (2025) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-24-01343 · Cited by 37
Stem cell models of human synapse development and degeneration
Wilson, E. S., & Litwa, K. (2018) · Molecular Biology of the Cell · doi:10.1091/mbc.e18-04-0222 · Cited by 30
Fleck, D., Phu, L., Verschueren, E., Hinkle, T. B., Reichelt, M., Bhangale, T., Haley, B., Wang, Y., Graham, R., Kirkpatrick, D. S., et al. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.0116-19.2019 · Cited by 31
Self-citationRoyea, J., Lacalle‐Aurioles, M., Trigiani, L. J., Fermigier, A., & Hamel, É. (2020) · Hypertension · doi:10.1161/hypertensionaha.119.14431 · Cited by 30
“lated to the sustained microglial activation in C21-treated APP mice, reactive microglia being involved in clearing Aβ aggregates.(45)”
BackgroundMicroglia in Alzheimer's Disease: The Role of Stem Cell-Microglia Interaction in Brain Homeostasis
Bagheri‐Mohammadi, S. (2020) · Neurochemical Research · doi:10.1007/s11064-020-03162-4 · Cited by 30
Sefiani, A., & Geoffroy, C. G. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.682259 · Cited by 31
Microglial transcription profiles in mouse and human are driven by APOE4 and sex
Moser, V. A., Workman, M. J., Hurwitz, S. J., Lipman, R. M., Pike, C. J., & Svendsen, C. N. (2021) · iScience · doi:10.1016/j.isci.2021.103238 · Cited by 29
Wang, Z., Zhang, Q., Lin, J.-R., Jabalameli, M. R., Mitra, J., Nguyen, N., & Zhang, Z. D. (2021) · Scientific Reports · doi:10.1038/s41598-021-99352-3 · Cited by 29
Mielcarska, M. B., Skowrońska, K., Wyżewski, Z., & Toka, F. N. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms23010242 · Cited by 32
Plant polysaccharides utilized by gut microbiota: New players in ameliorating cognitive impairment
Sun, Y., Ho, C., Zhang, Y., Hong, M., & Zhang, X. (2022) · Journal of Traditional and Complementary Medicine · doi:10.1016/j.jtcme.2022.01.003 · Cited by 32
Hausrat, T. J., Janiesch, P. C., Breiden, P., Lutz, D., Hoffmeister‐Ullerich, S., Hermans‐Borgmeyer, I., Failla, A. V., & Kneussel, M. (2022) · Nature Communications · doi:10.1038/s41467-022-31776-5 · Cited by 29
Common Signaling Pathways Involved in Alzheimer’s Disease and Stroke: Two Faces of the Same Coin
Das, T. K., Ganesh, B. P., & Fatima-Shad, K. (2023) · Journal of Alzheimer s Disease Reports · doi:10.3233/adr-220108 · Cited by 33
“It is mainly mediated by microglia [86, 87], oligodendrocytes [88, 89], and astrocytes [90, 91] in the brain.”
BackgroundZeng, L., Fujita, M., Gao, Z., White, C. C., Green, G. S., Habib, N., Menon, V., Bennett, D. A., Boyle, P. A., Klein, H., et al. (2023) · Biological Psychiatry · doi:10.1016/j.biopsych.2023.12.012 · Cited by 31
Terpenes as Potential Anti-Alzheimer’s Disease Agents
Lima, E., & Medeiros, J. (2024) · Applied Sciences · doi:10.3390/app14093898 · Cited by 31
Neutrophil to lymphocyte ratio in Alzheimer’s disease: A systematic review and meta-analysis
Mohammadi, A., Mohammadi, M., Almasi‐Dooghaee, M., & Mirmosayyeb, O. (2024) · PLoS ONE · doi:10.1371/journal.pone.0305322 · Cited by 30
Stem cell therapies for Alzheimer's disease
Wang, S., Lee, C., & Lim, H. K. (2018) · Current Opinion in Psychiatry · doi:10.1097/yco.0000000000000478 · Cited by 32
Plasminogen Activators in Neurovascular and Neurodegenerative Disorders
Yepes, M., Woo, Y., & Martín-Jiménez, C. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22094380 · Cited by 28
“However, more recent studies have revealed that microglial activation in AD is a heterogenous process, and in line with these observations, specific and well-differentiated subpopulations of microglia also seem to have a protective effect in the brain of AD patients [140].”
ResultKshirsagar, V. V., Thingore, C., Gursahani, M., Gawali, N. B., & Juvekar, A. R. (2021) · Neurotoxicity Research · doi:10.1007/s12640-021-00374-6 · Cited by 30
“Microglial activation leads to the formation of proinflammatory cytokines causing activation of macrophages and monocytes, leading to neurodegeneration (Navarro et al. 2018; Hansen et al. 2018).”
BackgroundMicroglia and its Genetics in Alzheimer's Disease
Liang, X., Wu, H., Colt, M., Guo, X., Pluimer, B. R., Zeng, J., Dong, S., & Zhao, Z. (2021) · Current Alzheimer Research · doi:10.2174/1567205018666211105140732 · Cited by 32
Sex and region-specific effects of variable stress on microglia morphology
Tsyglakova, M., Huskey, A., Hurst, E. H., Telep, N. M., Wilding, M. C., Babington, M. E., Rainville, J. R., & Hodes, G. E. (2021) · Brain Behavior & Immunity - Health · doi:10.1016/j.bbih.2021.100378 · Cited by 32
“This is somewhat a puzzling discovery, as we have found that both variable stress and rosiglitazone treatment cause changes in microglial morphology, shifting it to a more activated state, normally a hallmark of MDD as well as other psychiatric disorders (Gandal et al., 2018a, 2018b; Hansen et al., 2018; Setiawan et a…”
BackgroundLipocalin-2 Regulates Hippocampal Microglial Activation in Poststroke Depression
Li, W., Du, Y., Xie, Y., Yu, X., Chen, H., & Qiu, Y. (2021) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2021.798335 · Cited by 30
“Conclusion: Hippocampal microglia are activated during PSD; LCN2 may regulate hippocampal microglial activation by the P38 MAPK pathway in the process of PSD. Keywords: poststroke depression (PSD), microglia, hippocampi, Lipocalin-2 (Lcn2), p38 mitogen-activated protein kinase (p38 MAPK) Abbreviations: PSD, Poststroke…”
BackgroundInfluentialGanz, T., Fainstein, N., Elad, A., Lachish, M., Goldfarb, S., Einstein, O., & Ben‐Hur, T. (2022) · Journal of Neuroinflammation · doi:10.1186/s12974-021-02369-8 · Cited by 31
“Importantly, there are several populations of microglia in the AD brain, with different specializations, in which some are neurotoxic and others are neuroprotective (62,63).”
BackgroundRamesh, M., Balachandra, C., Andhare, P., & Govindaraju, T. (2022) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.2c00276 · Cited by 30
Alzheimer's disease and synapse Loss: What can we learn from induced pluripotent stem Cells?
Rodríguez-Jiménez, F. J., Ureña‐Peralta, J. R., Jendelová, P., & Erceg, S. (2023) · Journal of Advanced Research · doi:10.1016/j.jare.2023.01.006 · Cited by 33
“The proliferation and activation of microglia concentrated around A b plaques represent prominent hallmarks of AD [158].”
BackgroundGenetic insights into immune mechanisms of Alzheimer’s and Parkinson’s disease
Nott, A., & Holtman, I. R. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1168539 · Cited by 33
“For example, microglia that surround amyloid beta plaques were described as proliferative and activated and were suggested to restrict amyloid beta propagation and toxicity, thereby exerting a protective role (69, 70).”
BackgroundMethodInfluentialWang, X., Xie, Y., Chen, G., Lu, Y., Wang, D., & Li, Z. (2023) · Journal of Neuroinflammation · doi:10.1186/s12974-023-02931-6 · Cited by 33
Daniels, M. J. D., Lefèvre, L., Szymkowiak, S., Drake, A., McCulloch, L. J., Tzioras, M., Barrington, J., Dando, O., He, X., Mohammad, M., et al. (2023) · eLife · doi:10.7554/elife.85279 · Cited by 29
Botchway, B. O., Okoye, F. C., Chen, Y., Arthur, W. E., & Fang, M. (2022) · Aging and disease · doi:10.14336/ad.2021.0616 · Cited by 32
“Nonetheless, chronic inflammation causes the overproduction of free radical species and leads to oxidative stress, impairing the neuronal membrane [14, 15].”
BackgroundLymphoid gene expression supports neuroprotective microglia function
Ayata, P., Crowley, J. M., Challman, M. F., Sahasrabuddhe, V., Gratuze, M., Werneburg, S., Ribeiro, D., Hays, E. C., Durán-Laforet, V., Faust, T. E., et al. (2025) · Nature · doi:10.1038/s41586-025-09662-z · Cited by 32
Fremuth, L. E., Hu, H., van de Vlekkert, D., Annunziata, I., Weesner, J. A., & d’Azzo, A. (2025) · Cell Reports · doi:10.1016/j.celrep.2024.115204 · Cited by 29
“14 In Neu1 −/− mice, increased exocytosis of A β -42, a potent microglia activator, most likely induces a microglia-mediated neuroinflammatory response resembling AD, which provides a unique platform to examine how Neu1 regulates microglial function in neurodegenerative diseases.”
Metabolic stress and age drive inflammation and cognitive decline in mice and humans
Elzinga, S. E., Guo, K., Turfah, A., Henn, R. E., Webber‐Davis, I. F., Hayes, J. M., Pacut, C. M., Teener, S. J., Carter, A., Rigan, D. M., et al. (2025) · Alzheimer s & Dementia · doi:10.1002/alz.70060 · Cited by 35
Khan, M. S., Qureshi, N., Khan, R., Son, Y., & Maqbool, T. (2025) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2025.1578138 · Cited by 37
Richter, M., Vidovic, N., Biber, K. P. H., Dolga, A. M., Culmsee, C., & Dodel, R. C. (2019) · Brain Pathology · doi:10.1111/bpa.12807 · Cited by 31
“By reducing the Aβ load in the brain, microglia are thought to contribute to neuroprotection against AD pathology (21, 30, 31).”
BackgroundYeo, I. J., Lee, M. J., Baek, A., Miller, Z. C., Bhattarai, D., Baek, Y. M., Jeong, H. J., Kim, Y. K., Kim, D., Hong, J. T., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-54846-z · Cited by 29
Update of Immunosenescence in Cerebral Small Vessel Disease
Jian, B., Hu, M., Cai, W., Zhang, B., & Lu, Z. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.585655 · Cited by 33
“Immunosenescence is also considered as a candidate mechanism of AD, because the accumulation of Ab is closely associated with impaired clearance ability and cytotoxic effect of senescent microglia (48).”
BackgroundAlzheimer and Purinergic Signaling: Just a Matter of Inflammation?
Merighi, S., Poloni, T. E., Terrazzan, A., Moretti, E., Gessi, S., & Ferrari, D. (2021) · Cells · doi:10.3390/cells10051267 · Cited by 30
“Therefore, the loss of balance in the processes of immunity and inflammation, especially in old age, results in damage [84,85,122,123].”
BackgroundTheoharides, T. C. (2021) · Journal of Personalized Medicine · doi:10.3390/jpm11090860 · Cited by 29
Metadata
- Authors
- Hansen, D. V., Hanson, J. E., & Sheng, M.
- Affiliations
- Genentech (US)
- Corresponding author
- Hansen, David V.
- Sheng, Morgan
- Venue
- Journal of Cell Biology
- Publisher
- Rockefeller University Press
- Published
- 2017-12-01
- Volume
- 217
- Issue
- 2
- Pages
- 459-472
- ISSN
- 0021-9525 (ISSN-L)
- 1540-8140
- PMC
- PMC5800817
- OpenAlex
- W2774947569
- Semantic Scholar
- fecfe002f9c3883e4476d3ce0a69b874e06566f8
- Cited by
- 1,935
- References
- 184
- Citations by year
- 2026: 208 · 2025: 296 · 2024: 296 · 2023: 305 · 2022: 271 · 2021: 241 · 2020: 173 · 2019: 110 · 2018: 33 · 2017: 2
- FWCI
- 8.39
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- The Journal of Cell Biology (publishedVersion, cc-by-nc-sa)
- Europe PMC (PubMed Central) (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion, cc-by-nc-sa)
- PubMed (publishedVersion)
- Funders
- Genentech
- Topics
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Alzheimer's disease research and treatments
- Life Sciences › Neuroscience › Neurology › Neurological Disease Mechanisms and Treatments
- Keywords
- microglia, Alzheimer's disease, microglial activation, amyloid plaques, amyloid-beta, risk genes, synaptic loss, tau pathology, neuroinflammation, astrocyte activation, microglial activation states, neurodegeneration
- MeSH terms
- Alzheimer Disease, Animals, Brain, Humans, Microglia
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.
A language model drew the claims from the paper on 2026-10-06, under version 3 of the claim definition (model deepseek-v4.1-flash, prompt extract-v3).
A second model labelled each claim on 2026-10-06 (model jev-1.13-20260917, definition revision gold-guideline-v0.2).
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 ›
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