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Apoptosis Inducing Factor Is Involved in Stretch‐Induced Apoptosis of Myoblast via a Caspase‐9 Independent Pathway
Author(s) -
Wang Fang,
Wei ZhuLiang,
Sun XianRui,
Zhang Qiang,
Zhang CaiXia,
Jiang WenXin,
Yan Xiao,
Liu JiaNing,
Yuan Xiao
Publication year - 2017
Publication title -
journal of cellular biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.028
H-Index - 165
eISSN - 1097-4644
pISSN - 0730-2312
DOI - 10.1002/jcb.25759
Subject(s) - apoptosis , apoptosis inducing factor , microbiology and biotechnology , caspase , myocyte , blot , caspase 3 , caspase 8 , chemistry , caspase 9 , intrinsic apoptosis , biology , programmed cell death , biochemistry , gene
The apoptosis of myoblast in response to excessive cyclic stretch is crucial in adaptive construction of skeletal muscles in orthopedic functional therapy. Mitochondria signaling pathway is the central links in the execution of the intrinsic apoptotic cascade, but its molecular mechanism in stretch‐induced apoptosis in myoblasts remains incompletely understood. The aim of this study was to investigate the mechanobiological roles of caspase‐9 and Apoptosis Inducing Factor (AIF), two important components in mitochondrial pathway, in stretch‐induced apoptosis of myoblast. Hoechst 33258 was used to observe apoptotic cells morphologically and flow cytometry to analyze apoptosis rate of myoblasts. Protein and mRNA of caspase‐9 and AIF were detected by Western blotting and RT‐PCR. Furthermore, caspase‐9 specific inhibitor z‐LEHD‐fmk was applied to clear the mechanism of caspase‐9 pathway in stretch‐induced apoptosis. We found that apoptotic rate induced by cyclic stretch increased in a time‐dependent manner, and the same tendency of mRNA and protein of caspase‐9 and AIF. Caspase‐9 inhibition reduced stretch‐induced apoptosis, but had no effect on expression of AIF. We concluded that caspase‐9 and AIF played an important role in stretch‐induced apoptosis in myoblast, and AIF was involved in the process in a caspase‐9 independent way. J. Cell. Biochem. 118: 829–838, 2017. © 2016 Wiley Periodicals, Inc.