articleNature AgingSep 20, 2022HYBRID OA

Complement C1q-dependent excitatory and inhibitory synapse elimination by astrocytes and microglia in Alzheimer’s disease mouse models

Broad Institute · Brocade (United States) · +3 more institutions

PubMed
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Abstract

Abstract Microglia and complement can mediate neurodegeneration in Alzheimer’s disease (AD). By integrative multi-omics analysis, here we show that astrocytic and microglial proteins are increased in Tau P301S synapse fractions with age and in a C1q-dependent manner. In addition to microglia, we identified that astrocytes contribute substantially to synapse elimination in Tau P301S hippocampi. Notably, we found relatively more excitatory synapse marker proteins in astrocytic lysosomes, whereas microglial lysosomes contained more inhibitory synapse material. C1q deletion reduced astrocyte–synapse association and decreased astrocytic and microglial synapses engulfment in Tau P301S mice and rescued synapse…

Citation impact

314
total citations
FWCI
22.85
Percentile
100%
References
72
Citations per year

Authors

22

Topics & keywords

Keywords
  • Microglia
  • Synapse
  • Neurodegeneration
  • Neuroscience
  • Astrocyte
  • Excitatory synapse
  • Inhibitory postsynaptic potential
  • Biology
UN Sustainable Development Goals
  • Good health and well-being
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