NADPH oxidase 4 contributes to myoblast fusion and skeletal muscle regeneration

Cited 11 time in scopus
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Title
NADPH oxidase 4 contributes to myoblast fusion and skeletal muscle regeneration
Author(s)
Tae Hyun Yeom; S H Woo; Eun Soo KwonSung Sup Park
Bibliographic Citation
Oxidative Medicine and Cellular Longevity, vol. 2019, pp. 3585390-3585390
Publication Year
2019
Abstract
Myoblast fusion is an essential step in skeletal muscle development and regeneration. NADPH oxidase 4 (Nox4) regulates cellular processes such as proliferation, differentiation, and survival by producing reactive oxygen species (ROS). Insulin-like growth factor 1 induces muscle hypertrophy via Nox4, but its function in myoblast fusion remains elusive. Here, we report a ROS-dependent role of Nox4 in myoblast differentiation. Regenerating muscle fibers after injury by cardiotoxin had a lower cross-sectional area in Nox4-knockout (KO) mice than myofibers in wild-type (WT) mice. Diameters and fusion index values of myotubes differentiated from Nox4-KO primary myoblasts were significantly lower than those of myotubes derived from WT myoblasts. However, no difference was observed in the differentiation index and expression of MyoD, myogenin, and myosin heavy chain 3 (MHC) between KO and WT myotubes. The decreased fusion index was also observed during differentiation of primary myoblasts and C2C12 cells with suppressed Nox4 expression. In contrast, in C2C12 cells overexpressing Nox4, the fusion index was increased, whereas the differentiation index and MHC and myogenin protein expression were not affected compared to control. Interestingly, the expression of myomaker (Tmem8c), a fusogenic protein that controls myoblast fusion, was reduced in Nox4-knockdown C2C12 cells. The myomaker expression level was proportional to the cellular ROS level, which was regulated by of Nox4 expression level. These results suggests that Nox4 contributes to myoblast fusion, possibly through the regulation of myomaker expression via ROS production, and that Nox4-dependent ROS may promote skeletal muscle regeneration and growth.
ISSN
1942-0900
Publisher
Hindawi Ltd
DOI
http://dx.doi.org/10.1155/2019/3585390
Type
Article
Appears in Collections:
Aging Convergence Research Center > 1. Journal Articles
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