Low culture temperature inhibits myogenic differentiation through mitochondrial activity

Zoolog Sci. 2015 Apr;32(2):129-34. doi: 10.2108/zs140247.

Abstract

A previous study by our group reported that mouse and human myoblasts fail to express myogenin and to fuse into multi-nucleate myotubes when cultured at low temperature, such as 30°C, but that this activity is rescued by adding IGF-I and vitamin C to the culture medium. In the present study, we examined mitochondrial activity as a target of the inhibitory effects of the low culture temperature. It has been suggested that mitochondria regulate myogenesis. By using a mouse myoblast cell line C2C12, we demonstrate that the expression of cytochrome c oxidase subunit I (COX I), which is encoded in mitochondrial genome, increases during myogenic differentiation at the normal culture temperature (38°C), but that this up-regulation is inhibited at 30°C. The mitochondrial membrane potential also decreased at 30°C compared to the culture at 38°C. However, IGF-I and vitamin C rescued both COX I expression and mitochondrial membrane potential at 30°C as promoting muscle differentiation. We also find that the rescue of mitochondrial activity by IGF-I and vitamin C at 30°C occurred after the myogenin expression, which suggests that myogenin regulates mitochondrial function during myogenesis. We suggest that our low temperature-culture system may be suitable for use in studying the detailed mechanism of myogenin-related phenomena during myogenesis.

Keywords: IGF; mitochondria; myogenesis; myogenin; skeletal muscle; temperature; vitamin C.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Ascorbic Acid / pharmacology
  • Cell Culture Techniques
  • Cell Differentiation / physiology*
  • Cell Line
  • Cold Temperature*
  • Electron Transport Complex IV / genetics
  • Electron Transport Complex IV / metabolism
  • Gene Expression Regulation, Enzymologic
  • Insulin-Like Growth Factor I / pharmacology
  • Membrane Potential, Mitochondrial / physiology
  • Mice
  • Mitochondria / physiology*
  • Myoblasts / physiology*

Substances

  • Insulin-Like Growth Factor I
  • Electron Transport Complex IV
  • Ascorbic Acid