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. Author manuscript; available in PMC: 2022 Mar 15.
Published in final edited form as: J Alzheimers Dis. 2017;57(4):1123–1135. doi: 10.3233/JAD-161123

Table 2.

Selected studies on astrocyte-mediated synaptic pruning during development and neurodegeneration

Material used Molecules investigated Inhibitors used Summary References
Megf10 KO and Mertk KO mice MEGF10 and MERTK Genetic deletion of Megf10 and Mertk Astrocytes mediate synapse elimination through MEGF10 and MERTK pathways. Chung, 2013 [41]
APOE KI mice APOE2, APOE3, and APOE4 Genetic knock-in of human APOE APOE can facilitate or inhibit the astrocyte-mediated phagocytosis with the presence of opsonins. Chung, 2016 [42]
Il1a KO, Tnf KO, C1qa KO mice, Huntington’s and Alzheimer’s diseases, and amyotrophic lateral sclerosis patient brain tissue IL-1α, TNF, C1q, C3 Genetic deletion of Il1a, Tnf, C1qa Reactive microglia can secrete cytokines that induce reactive astrocytes, which in turn upregulate complement-mediated synaptic loss and also secrete neurotoxic factors to kill a subset of neurons and oligodendrocytes in multiple neurodegenerative conditions. Liddelow, 2017 [47]