Activation of insulin-like growth factor II expression during skeletal muscle regeneration in the rat: correlation with myotube formation

Mol Endocrinol. 1992 Aug;6(8):1227-34. doi: 10.1210/mend.6.8.1406701.

Abstract

Insulin-like growth factors (IGFs) are important stimulators of proliferation and differentiation of cultured myoblasts. It has previously been shown that IGF-I is induced during muscle regeneration in rodents, however, little is known about the expression of IGF-II. Therefore, two in vivo models were used to analyze IGF-II mRNA expression during skeletal muscle regeneration in the rat: injection of the snake venom notexin and induction of ischemia. During the regeneration process the levels of both IGF-I and IGF-II mRNA were transiently induced, as analyzed by solution hybridization. Both IGF-I-like immunoreactivity and IGF-II-like immunoreactivity were found to be present during muscle regeneration. In a time course study, induction of IGF-II was preceded by IGF-I, both at the mRNA and protein levels. Using alpha- and beta-actin as markers for different stages of skeletal muscle differentiation, together with the immunohistochemistry data, it is concluded that the expression of IGF-I and IGF-II occurs at different differentiation stages, and that IGF-II appears concomitant to the formation of myotubes. These results suggest that each IGF has a distinct role during the differentiation of muscle cells.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Northern
  • Elapid Venoms
  • Gene Expression Regulation / physiology
  • Immunoenzyme Techniques
  • Insulin-Like Growth Factor I / biosynthesis
  • Insulin-Like Growth Factor II / biosynthesis*
  • Insulin-Like Growth Factor II / genetics
  • Ischemia / metabolism
  • Male
  • Muscles / blood supply
  • Muscles / pathology
  • Muscles / physiology*
  • Necrosis
  • Nucleic Acid Hybridization
  • RNA, Messenger / biosynthesis
  • Rats
  • Rats, Sprague-Dawley
  • Regeneration / physiology*

Substances

  • Elapid Venoms
  • RNA, Messenger
  • notexin
  • Insulin-Like Growth Factor I
  • Insulin-Like Growth Factor II