| Literature DB >> 31433986 |
Tiffany Wu1, Borislav Dejanovic1, Vineela D Gandham2, Alvin Gogineni2, Rose Edmonds3, Stephen Schauer3, Karpagam Srinivasan1, Melanie A Huntley4, Yuanyuan Wang1, Tzu-Ming Wang1, Maj Hedehus2, Kai H Barck2, Maya Stark5, Hai Ngu5, Oded Foreman5, William J Meilandt1, Justin Elstrott2, Michael C Chang3, David V Hansen1, Richard A D Carano2, Morgan Sheng1, Jesse E Hanson6.
Abstract
Complement pathway overactivation can lead to neuronal damage in various neurological diseases. Although Alzheimer's disease (AD) is characterized by β-amyloid plaques and tau tangles, previous work examining complement has largely focused on amyloidosis models. We find that glial cells show increased expression of classical complement components and the central component C3 in mouse models of amyloidosis (PS2APP) and more extensively tauopathy (TauP301S). Blocking complement function by deleting C3 rescues plaque-associated synapse loss in PS2APP mice and ameliorates neuron loss and brain atrophy in TauP301S mice, improving neurophysiological and behavioral measurements. In addition, C3 protein is elevated in AD patient brains, including at synapses, and levels and processing of C3 are increased in AD patient CSF and correlate with tau. These results demonstrate that complement activation contributes to neurodegeneration caused by tau pathology and suggest that blocking C3 function might be protective in AD and other tauopathies.Entities:
Keywords: Alzheimer’s disease; C3; amyloidosis; astrocyte; complement; microglia; neurodegeneration; neuroinflammation; synapse; tauopathy
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Year: 2019 PMID: 31433986 DOI: 10.1016/j.celrep.2019.07.060
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423