Nature neuroscience · 2024
Regulation of cell distancing in peri-plaque glial nets by Plexin-B1 affects glial activation and amyloid compaction in Alzheimer's disease.
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Huang Yong, Wang Minghui, Ni Haofei, Zhang Jinglong, Li Aiqun, Hu Bin, Junqueira Alves Chrystian, Wahane Shalaka, Rios de Anda Mitzy, Ho Lap, Li Yuhuan, Kang Sangjo, Neff Ryan, Kostic Ana, Buxbaum Joseph D, Crary John F, Brennand Kristen J, Zhang Bin, Zou Hongyan, Friedel Roland H
Аннотация
Communication between glial cells has a profound impact on the pathophysiology of Alzheimer's disease (AD). We reveal here that reactive astrocytes control cell distancing in peri-plaque glial nets, which restricts microglial access to amyloid deposits. This process is governed by guidance receptor Plexin-B1 (PLXNB1), a network hub gene in individuals with late-onset AD that is upregulated in plaque-associated astrocytes. Plexin-B1 deletion in a mouse AD model led to reduced number of reactive astrocytes and microglia in peri-plaque glial nets, but higher coverage of plaques by glial processes, along with transcriptional changes signifying reduced neuroinflammation. Additionally, a reduced footprint of glial nets was associated with overall lower plaque burden, a shift toward dense-core-type plaques and reduced neuritic dystrophy. Altogether, our study demonstrates that Plexin-B1 regulates peri-plaque glial net activation in AD. Relaxing glial spacing by targeting guidance receptors may present an alternative strategy to increase plaque compaction and reduce neuroinflammation in AD.