2018
The identity and function of microglia in neurodegeneration
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Cited by 329 publications
(291 citation statements)
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“…MG showed the strongest transcriptional change (more DEGs, affected pathways, and activated diseases) than the two neuron types. This result is consistent with most previous studies, indicating that MG is one of the most sensitive cell types in mediating cognitive defects and neurodegeneration. − Microglia phagocytose cell debris and overproduce synapses under normal conditions, which facilitates the structural and functional recovery of impaired tissues. , Alternatively, microglia exhibit misdirected or excessive phagocytosis of normal neurons under pathological conditions, , which subsequently exacerbates brain injury. Evidence suggests that this detrimental form of phagocytosis of microglia may be attributed to inflammation or a subtoxic insult. , In the present study, after the functional analysis of DEGs in microglia, we identified significant activation of phagocytosis, neuronal apoptosis, and neuronal cell death processes after 0.5 μg/L BPF exposure.…”
Section: Discussionsupporting
confidence: 92%
“…MG showed the strongest transcriptional change (more DEGs, affected pathways, and activated diseases) than the two neuron types. This result is consistent with most previous studies, indicating that MG is one of the most sensitive cell types in mediating cognitive defects and neurodegeneration. − Microglia phagocytose cell debris and overproduce synapses under normal conditions, which facilitates the structural and functional recovery of impaired tissues. , Alternatively, microglia exhibit misdirected or excessive phagocytosis of normal neurons under pathological conditions, , which subsequently exacerbates brain injury. Evidence suggests that this detrimental form of phagocytosis of microglia may be attributed to inflammation or a subtoxic insult. , In the present study, after the functional analysis of DEGs in microglia, we identified significant activation of phagocytosis, neuronal apoptosis, and neuronal cell death processes after 0.5 μg/L BPF exposure.…”
Section: Discussionsupporting
confidence: 92%
“…4e). These results reflect that microglia and excitatory neurons are the primary cell types contributing to genetic risk for AD and SCZ, respectively, which is supported by the literature of AD and SCZ 28, 29 .…”
Section: Resultssupporting
confidence: 85%
“…4e). These results reflect that microglia and excitatory neurons are the primary cell types contributing to genetic risk for AD and SCZ, respectively, which is supported by the literature of AD and SCZ 28,29 . Subsequently, we select the genes regulated by the cell-type-specific CRRs related to SCZ or AD to perform gene ontology (GO) enrichment analysis.…”
Section: Script Understands the Pathogenic Mechanisms Of Ad And Scz I...supporting
confidence: 85%
“…Of note, the induced expression of MHCII (H2-Aa) was also confirmed on the protein level in mice and in human CNV membranes (Wieghofer et al, in press). The observed increase of Apoe expression further supports the induction of the DAM gene expression signature mediated by binding to the triggering receptor of myeloid cells 2 (TREM2), like it was shown in the brain (Song and Colonna, 2018). Furthermore, Apoe was highly expressed in DAM in a model of retinal light damage and, most importantly, in mononuclear phagocytes in the subretinal space in AMD patients (Levy et al, 2015a,b;O'Koren et al, 2019).…”
Section: Discussionsupporting
confidence: 58%

