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C5aR1 signaling promotes region- and age-dependent synaptic pruning in models of Alzheimer's disease
被引:2
|作者:
Gomez-Arboledas, Angela
[1
]
Fonseca, Maria I.
[1
]
Kramar, Eniko
[2
]
Chu, Shu-Hui
[1
]
Schartz, Nicole D.
[1
]
Selvan, Purnika
[1
]
Wood, Marcelo A.
[2
]
Tenner, Andrea J.
[1
,2
,3
]
机构:
[1] Univ Calif Irvine, Dept Mol Biol & Biochem, 3205 McGaugh Hall, Irvine, CA 92697 USA
[2] Univ Calif Irvine, Dept Neurobiol & Behav, Irvine, CA 92697 USA
[3] Univ Calif Irvine, Sch Med, Dept Pathol & Lab Med, Irvine, CA 92697 USA
关键词:
Alzheimer's disease;
C1q;
C5aR1;
LTP;
microglia;
synaptic pruning;
ALZHEIMERS-DISEASE;
COMPLEMENT ACTIVATION;
MOUSE MODELS;
MURINE MODELS;
C1Q;
EXPRESSION;
MICROGLIA;
RECEPTOR;
ELIMINATION;
AMYLOIDOSIS;
D O I:
10.1002/alz.13682
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
INTRODUCTION: Synaptic loss is a hallmark of Alzheimer's disease (AD) that correlates with cognitive decline in AD patients. Complement-mediated synaptic pruning has been associated with this excessive loss of synapses in AD. Here, we investigated the effect of C5aR1 inhibition on microglial and astroglial synaptic pruning in two mouse models of AD. METHODS: A combination of super-resolution and confocal and tridimensional image reconstruction was used to assess the effect of genetic ablation or pharmacological inhibition of C5aR1 on the Arctic48 and Tg2576 models of AD. RESULTS: Genetic ablation or pharmacological inhibition of C5aR1 partially rescues excessive pre-synaptic pruning and synaptic loss in an age and region-dependent fashion in two mouse models of AD, which correlates with improved long-term potentiation (LTP). DISCUSSION: Reduction of excessive synaptic pruning is an additional beneficial outcome of the suppression of C5a-C5aR1 signaling, further supporting its potential as an effective targeted therapy to treat AD.
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页码:2173 / 2190
页数:18
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