Muscle atrophy-related myotube-derived exosomal microRNA in neuronal dysfunction: Targeting both coding and long noncoding RNAs

Chia Pei Yang, Wan Shan Yang, Yu Hui Wong, Kai Hsuan Wang, Yuan Chi Teng, Ming Hsuan Chang, Ko Hsun Liao, Fang Shin Nian, Chuan Chuan Chao, Jin Wu Tsai, Wei Lun Hwang, Ming Wei Lin, Tsai Yu Tzeng, Pei Ning Wang, Mel Campbell, Liang Kung Chen, Ting Fen Tsai, Pei Ching Chang, Hsing Jien Kung

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4 引文 斯高帕斯(Scopus)

摘要

In mammals, microRNAs can be actively secreted from cells to blood. miR-29b-3p has been shown to play a pivotal role in muscle atrophy, but its role in intercellular communication is largely unknown. Here, we showed that miR-29b-3p was upregulated in normal and premature aging mouse muscle and plasma. miR-29b-3p was also upregulated in the blood of aging individuals, and circulating levels of miR-29b-3p were negatively correlated with relative appendicular skeletal muscle. Consistently, miR-29b-3p was observed in exosomes isolated from long-term differentiated atrophic C2C12 cells. When C2C12-derived miR-29b-3p-containing exosomes were uptaken by neuronal SH-SY5Y cells, increased miR-29b-3p levels in recipient cells were observed. Moreover, miR-29b-3p overexpression led to downregulation of neuronal-related genes and inhibition of neuronal differentiation. Interestingly, we identified HIF1α-AS2 as a novel c-FOS targeting lncRNA that is induced by miR-29b-3p through down-modulation of c-FOS and is required for miR-29b-3p-mediated neuronal differentiation inhibition. Our results suggest that atrophy-associated circulating miR-29b-3p may mediate distal communication between muscle cells and neurons.

原文英語
文章編號e13107
期刊Aging Cell
19
發行號5
DOIs
出版狀態已發佈 - 五月 1 2020

ASJC Scopus subject areas

  • 老化
  • 細胞生物學

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