GJA1 (connexin43) is a key regulator of Alzheimer’s disease pathogenesis

被引:0
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作者
Yuji Kajiwara
Erming Wang
Minghui Wang
Wun Chey Sin
Kristen J. Brennand
Eric Schadt
Christian C. Naus
Joseph Buxbaum
Bin Zhang
机构
[1] Icahn School of Medicine at Mount Sinai,Department of Psychiatry
[2] Icahn School of Medicine at Mount Sinai,Department of Genetics and Genomic Sciences
[3] Icahn School of Medicine at Mount Sinai,Mount Sinai Center for Transformative Disease Modeling, Icahn Institute of Genomics and Multiscale Biology
[4] University of British Columbia,Department of Cellular and Physiological Sciences
[5] Icahn School of Medicine at Mount Sinai,Department of Neuroscience
[6] Icahn School of Medicine at Mount Sinai,Friedman Brain Institute
[7] Current address: Denali Therapeutics,undefined
[8] ,undefined
关键词
Alzheimer’s disease; GJA1; Cx43; connexin43; Gene networks; amyloidβ; Astrocyte;
D O I
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摘要
GJA1 (connexin43) has been predicted as the top key driver of an astrocyte enriched subnetwork associated with Alzheimer’s disease (AD). In this study, we comprehensively examined GJA1 expression across 29 transcriptomic and proteomic datasets from post-mortem AD and normal control brains. We demonstrated that GJA1 was strongly associated with AD amyloid and tau pathologies and cognitive functions. RNA sequencing analysis of Gja1−/− astrocytes validated that Gja1 regulated the subnetwork identified in AD, and many genes involved in Aβ metabolism. Astrocytes lacking Gja1 showed reduced Apoe protein levels as well as impaired Aβ phagocytosis. Consistent with this, wildtype neurons co-cultured with Gja1−/− astrocytes contained higher levels of Aβ species than those with wildtype astrocytes. Moreover, Gja1−/− astrocytes was more neuroprotective under Aβ stress. Our results underscore the importance of GJA1 in AD pathogenesis and its potential for further investigation as a promising pharmacological target in AD.
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