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Leucine regulates slow‐twitch muscle fibers expression and mitochondrial function by Sirt1/ AMPK signaling in porcine skeletal muscle satellite cells
Author(s) -
Chen Xiaoling,
Xiang Lu,
Jia Gang,
Liu Guangmang,
Zhao Hua,
Huang Zhiqing
Publication year - 2019
Publication title -
animal science journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.606
H-Index - 38
eISSN - 1740-0929
pISSN - 1344-3941
DOI - 10.1111/asj.13146
Subject(s) - ampk , skeletal muscle , myosin , mitochondrion , leucine , microbiology and biotechnology , amp activated protein kinase , myocyte , chemistry , succinate dehydrogenase , biochemistry , biology , endocrinology , protein kinase a , phosphorylation , amino acid
A previous study demonstrated that leucine upregulates the slow myosin heavy chain mRNA expression in C2C12 cells. However, the role of leucine in slow‐twitch muscle fibers expression and mitochondrial function of porcine skeletal muscle satellite cells as well as its mechanism remain unclear. In this study, porcine skeletal muscle satellite cells cultured in differentiation medium were treated with 2 mM leucine for 3 days. Sirt1 inhibitor EX 527, AMPK inhibitor compound C, and AMPK α1 si RNA were used to examine its underlying mechanism. Here we showed that leucine increased slow‐twitch muscle fibers and mitochondrial function‐related gene expression, as well as increased succinic dehydrogenase ( SDH ) and malate dehydrogenase ( MDH ) activities. Moreover, leucine increased the protein levels of Sirt1 and phospho‐ AMPK . We also found that AMPK α1 si RNA , AMPK inhibitor compound C, or Sirt1 inhibitor EX 527 attenuated the positive effect of leucine on slow‐twitch muscle fibers and mitochondrial function‐related gene expression. Finally, we showed that Sirt1 was required for leucine‐induced AMPK activation. Our results provide, for the first time, evidence that leucine induces slow‐twitch muscle fibers expression and improves mitochondrial function through Sirt1/ AMPK signaling pathway in porcine skeletal muscle satellite cells.