On the public citation graph
Phagocytic Glial Cells in Brain Homeostasis
0 signed · 115 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
1 of the 79 references listed on this page is in the Retraction Watch database as retracted (export 2026-11-04): 10.1038/nn.3560 (notice 2022-01-13).
Dataset join, best-effort; this page does not check the publisher record. Retraction Watch data via Crossref Labs, used with credit; OpenCitations Index (CC0) and Meta (CC BY 4.0); dataset doi:10.7910/DVN/WT8VOA (CC BY 4.0).
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/glia.22619openalex-snapshot
Apolipoproteins E and J interfere with amyloid‐beta uptake by primary human astrocytes and microglia in vitro
inferredcites →https://doi.org/10.1002/glia.22873openalex-snapshot
Slow degradation in phagocytic astrocytes can be enhanced by lysosomal acidification
inferredcites →https://doi.org/10.1002/glia.23270openalex-snapshot
Phagocytic clearance of presynaptic dystrophies by reactive astrocytes in Alzheimer's disease
inferredcites →https://doi.org/10.1002/glia.23664openalex-snapshot
TREM2 is required for microglial instruction of astrocytic synaptic engulfment in neurodevelopment
inferredcites →https://doi.org/10.1002/glia.23943openalex-snapshot
Amyloid‐β impairs the phagocytosis of dystrophic synapses by astrocytes in Alzheimer's disease
inferredcites →https://doi.org/10.1007/s11481-012-9427-3openalex-snapshot
Amyloid-β-Induced Astrocytic Phagocytosis is Mediated by CD36, CD47 and RAGE
inferredcites →https://doi.org/10.1007/s13238-016-0269-2openalex-snapshot
Deacetylation of TFEB promotes fibrillar Aβ degradation by upregulating lysosomal biogenesis in microglia
inferredcites →https://doi.org/10.1016/j.bbi.2010.09.021openalex-snapshot
Brain-specific angiogenesis inhibitor-1 expression in astrocytes and neurons: Implications for its dual function as an apoptotic engulfment receptor
inferredcites →https://doi.org/10.1016/j.bcp.2014.01.008openalex-snapshot
Microglial dysfunction in brain aging and Alzheimer's disease
inferredcites →https://doi.org/10.1016/j.cell.2007.10.036openalex-snapshot
The Classical Complement Cascade Mediates CNS Synapse Elimination
inferredcites →https://doi.org/10.1016/j.celrep.2020.107530openalex-snapshot
IL-33-PU.1 Transcriptome Reprogramming Drives Functional State Transition and Clearance Activity of Microglia in Alzheimer’s Disease
inferredcites →https://doi.org/10.1016/j.immuni.2018.04.016openalex-snapshot
The Microglial Innate Immune Receptor TREM2 Is Required for Synapse Elimination and Normal Brain Connectivity
inferredcites →https://doi.org/10.1016/j.isci.2019.05.039openalex-snapshot
CD4 T Cells Induce A Subset of MHCII-Expressing Microglia that Attenuates Alzheimer Pathology
inferredcites →https://doi.org/10.1016/j.jneuroim.2012.06.004openalex-snapshot
Scavenger receptor class A ligands induce secretion of IL1β and exert a modulatory effect on the inflammatory activation of astrocytes in culture
inferredcites →https://doi.org/10.1016/j.neulet.2019.134317openalex-snapshot
Microglial clearance of focal apoptotic synapses
inferredcites →https://doi.org/10.1016/j.neuron.2012.03.026openalex-snapshot
Microglia Sculpt Postnatal Neural Circuits in an Activity and Complement-Dependent Manner
inferredcites →https://doi.org/10.1016/j.neuron.2017.05.037openalex-snapshot
TDP-43 Depletion in Microglia Promotes Amyloid Clearance but Also Induces Synapse Loss
inferredcites →https://doi.org/10.1016/j.neuron.2018.09.017openalex-snapshot
CD47 Protects Synapses from Excess Microglia-Mediated Pruning during Development
inferredcites →https://doi.org/10.1016/j.neuroscience.2013.06.049openalex-snapshot
Increased lysosomal biogenesis in activated microglia and exacerbated neuronal damage after traumatic brain injury in progranulin-deficient mice
inferredcites →https://doi.org/10.1016/j.neuroscience.2020.07.016openalex-snapshot
Engulfment of Toxic Amyloid β-protein in Neurons and Astrocytes Mediated by MEGF10
inferredcites →https://doi.org/10.1016/s0166-2236(98)01349-6openalex-snapshot
Tripartite synapses: glia, the unacknowledged partner
inferredcites →https://doi.org/10.1023/a:1026441907803openalex-snapshot
Lysosomal heterogeneity between and within cells with respect to resistance against oxidative stress
inferredcites →https://doi.org/10.1038/labinvest.2016.116openalex-snapshot
CD68/macrosialin: not just a histochemical marker
inferredcites →https://doi.org/10.1038/nature06329openalex-snapshot
BAI1 is an engulfment receptor for apoptotic cells upstream of the ELMO/Dock180/Rac module
inferredcites →https://doi.org/10.1038/nature12776openalex-snapshot
Astrocytes mediate synapse elimination through MEGF10 and MERTK pathways
inferredcites →https://doi.org/10.1038/nature21029openalex-snapshot
Neurotoxic reactive astrocytes are induced by activated microglia
inferredcites →https://doi.org/10.1038/ncomms7176openalex-snapshot
Microglia constitute a barrier that prevents neurotoxic protofibrillar Aβ42 hotspots around plaques
inferredcites →https://doi.org/10.1038/nn.3560openalex-snapshot
RETRACTED ARTICLE: TGF-β signaling regulates neuronal C1q expression and developmental synaptic refinement
inferredcites →https://doi.org/10.1038/nn.4132openalex-snapshot
Depletion of microglia and inhibition of exosome synthesis halt tau propagation
inferredcites →https://doi.org/10.1038/nrn.2017.36openalex-snapshot
Progranulin, lysosomal regulation and neurodegenerative disease
inferredcites →https://doi.org/10.1038/s41467-017-00037-1openalex-snapshot
Reactive astrocytes function as phagocytes after brain ischemia via ABCA1-mediated pathway
inferredcites →https://doi.org/10.1038/s41467-020-19227-5openalex-snapshot
Gene expression and functional deficits underlie TREM2-knockout microglia responses in human models of Alzheimer’s disease
inferredcites →https://doi.org/10.1038/s41586-020-03060-3openalex-snapshot
Astrocytes phagocytose adult hippocampal synapses for circuit homeostasis
inferredcites →https://doi.org/10.1038/s41593-020-00757-6openalex-snapshot
Microglia facilitate repair of demyelinated lesions via post-squalene sterol synthesis
inferredcites →https://doi.org/10.1038/s41593-020-00763-8openalex-snapshot
Overexpression of schizophrenia susceptibility factor human complement C4A promotes excessive synaptic loss and behavioral changes in mice
inferredcites →https://doi.org/10.1038/s41593-020-00780-7openalex-snapshot
Phagocyte-mediated synapse removal in cortical neuroinflammation is promoted by local calcium accumulation
inferredcites →https://doi.org/10.1038/s41593-020-0624-8openalex-snapshot
Disease-associated astrocytes in Alzheimer’s disease and aging
inferredcites →https://doi.org/10.1038/s41593-020-0672-0openalex-snapshot
The endogenous neuronal complement inhibitor SRPX2 protects against complement-mediated synapse elimination during development
inferredcites →https://doi.org/10.1038/s41598-020-66292-3openalex-snapshot
Cilostazol restores autophagy flux in bafilomycin A1-treated, cultured cortical astrocytes through lysosomal reacidification: roles of PKA, zinc and metallothionein 3
inferredcites →https://doi.org/10.1039/d1sc03486copenalex-snapshot
Monitoring phagocytic uptake of amyloid β into glial cell lysosomes in real time
inferredcites →https://doi.org/10.1073/pnas.1609896113openalex-snapshot
Novel allele-dependent role for APOE in controlling the rate of synapse pruning by astrocytes
inferredcites →https://doi.org/10.1073/pnas.1801612115openalex-snapshot
Amyloid clearance defect in ApoE4 astrocytes is reversed by epigenetic correction of endosomal pH
inferredcites →https://doi.org/10.1083/jcb.201701047openalex-snapshot
The spread of prion-like proteins by lysosomes and tunneling nanotubes: Implications for neurodegenerative diseases
inferredcites →https://doi.org/10.1084/jem.20041611openalex-snapshot
Clearance of apoptotic neurons without inflammation by microglial triggering receptor expressed on myeloid cells-2
inferredcites →https://doi.org/10.1085/jgp.201110596openalex-snapshot
Lysosomal pH and analysis of the counter ion pathways that support acidification
inferredcites →https://doi.org/10.1091/mbc.e06-10-0975openalex-snapshot
Activation of Microglia Acidifies Lysosomes and Leads to Degradation of Alzheimer Amyloid Fibrils
inferredcites →https://doi.org/10.1093/jnen/61.9.760openalex-snapshot
Astrocytes Are Less Efficient in the Removal of Apoptotic Lymphocytes than Microglia Cells: Implications for the Role of Glial Cells in the Inflamed Central Nervous System
inferredcites →https://doi.org/10.1101/cshperspect.a028761openalex-snapshot
Mechanosensing and Mechanotransduction at Cell–Cell Junctions
inferredcites →https://doi.org/10.1101/gad.229518.113openalex-snapshot
Astrocytes engage unique molecular programs to engulf pruned neuronal debris from distinct subsets of neurons
inferredcites →https://doi.org/10.1126/sciadv.aba3239openalex-snapshot
Astrocytes and microglia play orchestrated roles and respect phagocytic territories during neuronal corpse removal in vivo
inferredcites →https://doi.org/10.1126/science.1202529openalex-snapshot
Synaptic Pruning by Microglia Is Necessary for Normal Brain Development
inferredcites →https://doi.org/10.1126/science.aal3589openalex-snapshot
Astrocyte-derived interleukin-33 promotes microglial synapse engulfment and neural circuit development
inferredcites →https://doi.org/10.1126/science.aaz2288openalex-snapshot
Microglia mediate forgetting via complement-dependent synaptic elimination
inferredcites →https://doi.org/10.1155/2016/4732837openalex-snapshot
Transcription Factor EB Is Selectively Reduced in the Nuclear Fractions of Alzheimer’s and Amyotrophic Lateral Sclerosis Brains
inferredcites →https://doi.org/10.1159/000337115openalex-snapshot
Copper-Zinc Superoxide Dismutase (SOD1) Is Released by Microglial Cells and Confers Neuroprotection against 6-OHDA Neurotoxicity
inferredcites →https://doi.org/10.1186/s12974-020-01776-7openalex-snapshot
Astrocytes have the capacity to act as antigen-presenting cells in the Parkinson’s disease brain
inferredcites →https://doi.org/10.1186/s13024-016-0098-zopenalex-snapshot
Accumulation of amyloid-β by astrocytes result in enlarged endosomes and microvesicle-induced apoptosis of neurons
inferredcites →https://doi.org/10.1186/s13024-018-0281-5openalex-snapshot
Early lysosomal maturation deficits in microglia triggers enhanced lysosomal activity in other brain cells of progranulin knockout mice
inferredcites →https://doi.org/10.1186/s13064-018-0104-yopenalex-snapshot
Astrocytes, neurons, synapses: a tripartite view on cortical circuit development
inferredcites →https://doi.org/10.1371/journal.pone.0033090openalex-snapshot
Engulfing Astrocytes Protect Neurons from Contact-Induced Apoptosis following Injury
inferredcites →https://doi.org/10.1371/journal.pone.0094197openalex-snapshot
Activated Scavenger Receptor A Promotes Glial Internalization of Aβ
inferredcites →https://doi.org/10.1371/journal.pone.0155878openalex-snapshot
Low Density Lipoprotein-Receptor Related Protein 1 Is Differentially Expressed by Neuronal and Glial Populations in the Developing and Mature Mouse Central Nervous System
inferredcites →https://doi.org/10.1523/jneurosci.0336-15.2015openalex-snapshot
Elimination of Microglia Improves Functional Outcomes Following Extensive Neuronal Loss in the Hippocampus
inferredcites →https://doi.org/10.1523/jneurosci.1419-07.2007openalex-snapshot
Synaptic Islands Defined by the Territory of a Single Astrocyte
inferredcites →https://doi.org/10.1523/jneurosci.3442-16.2017openalex-snapshot
Astrocytic LRP1 Mediates Brain Aβ Clearance and Impacts Amyloid Deposition
inferredcites →https://doi.org/10.1523/jneurosci.3788-13.2014openalex-snapshot
Enhancing Astrocytic Lysosome Biogenesis Facilitates Aβ Clearance and Attenuates Amyloid Plaque Pathogenesis
inferredcites →https://doi.org/10.1523/jneurosci.3850-15.2016openalex-snapshot
Megf10 Is a Receptor for C1Q That Mediates Clearance of Apoptotic Cells by Astrocytes
inferredcites →https://doi.org/10.1523/jneurosci.4178-07.2008openalex-snapshot
A Transcriptome Database for Astrocytes, Neurons, and Oligodendrocytes: A New Resource for Understanding Brain Development and Function
inferredcites →https://doi.org/10.15252/embj.2020104464openalex-snapshot
Astrocytic phagocytosis is a compensatory mechanism for microglial dysfunction
inferredcites →https://doi.org/10.3389/fbioe.2020.596577openalex-snapshot
Fluid Shear Stress Enhances the Phagocytic Response of Astrocytes
inferredcites →https://doi.org/10.3389/fnagi.2017.00228openalex-snapshot
Amyloid β-Induced Redistribution of Transcriptional Factor EB and Lysosomal Dysfunction in Primary Microglial Cells
inferredcites →https://doi.org/10.3389/fncel.2013.00006openalex-snapshot
Janus-faced microglia: beneficial and detrimental consequences of microglial phagocytosis
inferredcites →https://doi.org/10.3389/fneur.2019.00099openalex-snapshot
Astrocyte Mechano-Activation by High-Rate Overpressure Involves Alterations in Structural and Junctional Proteins
inferredcites →https://doi.org/10.4049/jimmunol.162.1.480openalex-snapshot
Phagocytosis Triggers Macrophage Release of Fas Ligand and Induces Apoptosis of Bystander Leukocytes
inferredcites →https://doi.org/10.4049/jimmunol.167.9.5004openalex-snapshot
Microglial Phagocytosis of Apoptotic Inflammatory T Cells Leads to Down-Regulation of Microglial Immune Activation
inferredcites →https://doi.org/10.4062/biomolther.2012.20.3.245openalex-snapshot
Mechanisms of Amyloid-β Peptide Clearance: Potential Therapeutic Targets for Alzheimer's Disease
inferredcites →https://doi.org/10.4103/1673-5374.239449openalex-snapshot
SIRT1 facilitates amyloid beta peptide degradation by upregulating lysosome number in primary astrocytes
inferredcites →https://doi.org/10.7554/elife.54083openalex-snapshot
Fibrillar Aβ triggers microglial proteome alterations and dysfunction in Alzheimer mouse models
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4755485openalex-extracted
A Pharmacological Toolkit for Human Microglia Identifies Topoisomerase I Inhibitors as Immunomodulators for Alzheimer's Disease
inferred← citeshttps://doi.org/10.1002/glia.70025openalex-snapshot
Death in the Taste Bud: Engulfment of Dying Taste Receptor Cells by Glial‐Like Type I Cells
inferred← citeshttps://doi.org/10.1007/978-3-031-32035-4_144-1openalex-snapshot
Posttraumatic Stress Disorder (PTSD) and Glial Suppression
inferred← citeshttps://doi.org/10.1007/978-3-031-73368-0_144openalex-snapshot
Posttraumatic Stress Disorder (PTSD) and Glial Suppression
inferred← citeshttps://doi.org/10.1016/j.brainresbull.2023.110668openalex-snapshot
Impact of sex on neuroimmune contributions to Parkinson’s disease
inferred← citeshttps://doi.org/10.1016/j.celrep.2024.115201openalex-snapshot
Santa-maria is a glial phagocytic receptor that acts with SIMU to recognize and engulf apoptotic neurons
inferred← citeshttps://doi.org/10.1016/j.expneurol.2022.114239openalex-snapshot
Implications of microglial heterogeneity in spinal cord injury progression and therapy
inferred← citeshttps://doi.org/10.1016/j.focha.2024.100767openalex-snapshot
Protective effect and antioxidative efficacy of Moringa stenopetala leaf extract in BV-2 microglial cell
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2024.136832openalex-snapshot
Early-life exposure to PCBs and PFAS exerts negative effects on the developing central nervous system
inferred← citeshttps://doi.org/10.1016/j.mcn.2022.103804openalex-snapshot
Cardiolipin released by microglia can act on neighboring glial cells to facilitate the uptake of amyloid-β (1–42)
inferred← citeshttps://doi.org/10.1016/j.nbd.2026.107618openalex-snapshot
MERTK-dependent efferocytosis in Cx3cr1-expressing myeloid cells supports recovery after traumatic brain injury in male mice
inferred← citeshttps://doi.org/10.1016/j.neulet.2022.136852openalex-snapshot
Independent actions by HIV-1 Tat and morphine to increase recruitment of monocyte-derived macrophages into the brain in a region-specific manner
inferred← citeshttps://doi.org/10.1016/j.neulet.2025.138487openalex-snapshot
MEGF10 knockout promotes cortical and hippocampal amyloid deposition in AD mouse model
inferred← citeshttps://doi.org/10.1016/j.tox.2026.154499openalex-snapshot
Time-resolved multi-omics reveals staged mitochondrial dysfunction and neurodegeneration-related changes in a tri-culture BTX neurotoxicity model
inferred← citeshttps://doi.org/10.1038/s41420-023-01382-5openalex-snapshot
Drosophila FGFR/Htl signaling shapes embryonic glia to phagocytose apoptotic neurons
inferred← citeshttps://doi.org/10.1038/s41593-025-02115-wopenalex-snapshot
Astrocytic Sox9 overexpression in Alzheimer’s disease mouse models promotes Aβ plaque phagocytosis and preserves cognitive function
inferred← citeshttps://doi.org/10.1101/2024.02.06.579103openalex-snapshot
A pharmacological toolkit for human microglia identifies Topoisomerase I inhibitors as immunomodulators for Alzheimer’s disease
inferred← citeshttps://doi.org/10.1111/bph.17343openalex-snapshot
Plumbagin, a novel TRPV2 inhibitor, ameliorates microglia activation and brain injury in a middle cerebral artery occlusion/reperfusion mouse model
inferred← citeshttps://doi.org/10.1111/cns.13942openalex-snapshot
Relationship between chronic hypoxia and seizure susceptibility
inferred← citeshttps://doi.org/10.1177/13872877251374353openalex-snapshot
Neuroinflammation and Alzheimer's disease: Unravelling the molecular mechanisms
inferred← citeshttps://doi.org/10.1186/s12929-026-01215-4openalex-snapshot
Osmotin-derived 9-amino-acid peptide alleviates α-synuclein and MPTP-induced glial cell activation mediated neuroinflammation, protecting dopaminergic neurons in Parkinson’s disease mice brain
inferred← citeshttps://doi.org/10.1186/s12967-024-05769-5openalex-snapshot
Ion channels research in hPSC-RPE cells: bridging benchwork to clinical applications
inferred← citeshttps://doi.org/10.1371/journal.pbio.3002822openalex-snapshot
Experience-dependent serotonergic signaling in glia regulates targeted synapse elimination
inferred← citeshttps://doi.org/10.1515/znc-2025-0239openalex-snapshot
Phytomicronutrients in neurodegeneration: modulating microglial dynamics for neuroprotection
inferred← citeshttps://doi.org/10.15406/jccr.2024.17.00597openalex-snapshot
Hypoxic convulsions induced by adult respiratory distress syndrome in Covid-19 patient
inferred← citeshttps://doi.org/10.31718/2077-1096.23.3.237openalex-snapshot
GLIOCYTES OF THE BRAIN: CYTOLOGICAL AND FUNCTIONAL PECULIARITIES (LECTURE)
inferred← citeshttps://doi.org/10.3389/fimmu.2023.1228530openalex-snapshot
Melanin: a unifying theory of disease as exemplified by Parkinson’s, Alzheimer’s, and Lewy body dementia
inferred← citeshttps://doi.org/10.3389/fnhum.2025.1471433openalex-snapshot
Potential common targets of music therapy intervention in neuropsychiatric disorders: the prefrontal cortex-hippocampus -amygdala circuit (a review)
inferred← citeshttps://doi.org/10.3389/fnsyn.2023.1130198openalex-snapshot
Bringing synapses into focus: Recent advances in synaptic imaging and mass-spectrometry for studying synaptopathy
inferred← citeshttps://doi.org/10.3390/cells10102555openalex-snapshot
Comparative Review of Microglia and Monocytes in CNS Phagocytosis
inferred← citeshttps://doi.org/10.3390/cells11213414openalex-snapshot
Assaying Microglia Functions In Vitro
inferred← citeshttps://doi.org/10.3390/ijms26010057openalex-snapshot
The Critical Role of Autophagy and Phagocytosis in the Aging Brain
inferred← citeshttps://doi.org/10.3390/ijms27010296openalex-snapshot
Targeting Adipocyte Enhancer-Binding Protein 1 to Induce Microglial Phenotype Shift for Immunotherapy in Alzheimer’s Disease
inferred← citeshttps://doi.org/10.3390/nu16142244openalex-snapshot
Postbiotics as Molecules Targeting Cellular Events of Aging Brain—The Role in Pathogenesis, Prophylaxis and Treatment of Neurodegenerative Diseases
inferred← citeshttps://doi.org/10.35376/10324/51889openalex-snapshot
The insulin-degrading enzyme: from molecular evolution and subcellular localization to new roles in microglial physiology
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.