IL-17A promotes transdifferentiation of mouse myoblast cells (C2C12) into adipocytes by increasing the expression of peroxisome proliferator-activated receptor γ through CAAT/enhancer binding protein β signaling

Biotechnol Lett. 2011 Feb;33(2):229-35. doi: 10.1007/s10529-010-0440-4. Epub 2010 Oct 20.

Abstract

helper 17 T (Th17) effector cells are a recently identified Th subset and possess a unique property that distinguishes them from Th1 and Th2 subsets. The functional role of Th17 effector cells involves inflammatory responses, including autoimmunity and infection of specific pathogens. Therefore, IL-17A and its receptors may play a key role in determining the progression of certain inflammatory reactions. However, the relationship between IL-17A and adipogenesis has not yet been examined. Therefore, in this study, the effect of IL-17A on the adipogenic transdifferentiation of mouse myoblast (C2C12) cells was examined. CAAT/enhancer binding-protein β (C/EPBβ) signaling through the IL-17A receptor promoted adipogenic transdifferentiation of myoblast cells by activating peroxisome proliferator-activated receptor γ (PPARγ). These results will advance our understanding of the physiological function of IL-17A in myoblasts during inflammation, as well as the relationship between adipogenesis and inflammation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes / drug effects
  • Adipocytes / physiology*
  • Animals
  • CCAAT-Enhancer-Binding Proteins / metabolism*
  • Cell Transdifferentiation*
  • Interleukin-17 / metabolism*
  • Mice
  • Myoblasts / drug effects
  • Myoblasts / physiology*
  • PPAR gamma / biosynthesis*
  • Signal Transduction*

Substances

  • CCAAT-Enhancer-Binding Proteins
  • Interleukin-17
  • PPAR gamma