Author:
Sui Bingdong,Wang Runci,Chen Chider,Kou Xiaoxing,Wu Di,Tu Ho-Chou,Wang Yanzhuang,Liu Yijing,Jacobson Orit,Chen Xiaoyuan,Liu Haixiang,Kwok Ryan Tsz Kin,Tang Ben Zhong,Yan Hexin,Wang Minjun,Xiang Lei,Yan Xutong,Fu Yu,Zhang Xiao,Tang Jianxia,Ma Lan,Lu Lu,Jin Yan,Shi Songtao
Abstract
SummaryApoptosis is an integral physiological cell death process that occurs frequently and generates a huge number of apoptotic extracellular vesicles (apoEVs). However, whether apoEVs are necessary for maintaining organ homeostasis remains unclear. Here, we show that circulatory apoEVs engraft in liver and undergo specialized internalization by hepatocytes (HCs) based on surface signature of galactose and N-acetylgalactosamine. Furthermore, apoEVs rescue liver injury in apoptotic-deficient Fas mutant and Caspase-3 knockout mice, which is exerted by restoring the featured hepatic ploidy homeostasis. Surprisingly, apoEVs form a chimeric organelle complex with recipient Golgi apparatus via SNARE-mediated membrane interaction, which consequently facilitates microtubule organization and HC cytokinesis. Notably, through Golgi recovery and ploidy transition, apoEVs contribute to liver regeneration and protect against acute hepatic failure. Collectively, these results identify a previously unrecognized role for apoEVs and the specific mechanisms by which they safeguard liver homeostasis, and suggest the potential of apoEV-based therapy for liver disorders.
Publisher
Cold Spring Harbor Laboratory
Cited by
1 articles.
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