Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10751911 | Biochemical and Biophysical Research Communications | 2015 | 6 Pages |
Abstract
Cachexia or muscle wasting is a common condition that occurs in many chronic diseases. The wasting conditions are characterized by increased levels of TNF-α which was also known as cachectin in the past. But how TNF-α exerts its cachetic effects remains controversial. To clarify this issue, we investigated the impact of TNF-α on C2C12 cell myogenic differentiation. Our results demonstrate that myotube formation was completely inhibited by TNF-α when added to differentiating C2C12 myoblasts. The inhibitory effect of TNF-α on differentiation was accompanied by activation of NF-κB and down regulation of myogenin and Akt. Importantly, TNF-α's effect on differentiation was abolished when IGF-1 was added to the culture. IGF-1 treatment also inhibited NF-κB reporter activity and restored Akt levels. Our data suggest that TNF-α inhibits myogenic differentiation through NF-κB activation and impairment of IGF-1 signaling pathway. The reversal of TNF-α induced inhibition of myogenesis by IGF-1 may have significant therapeutic potential.
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Authors
Q. Zhao, S.T. Yang, J.J. Wang, J. Zhou, S.S. Xing, C.C. Shen, X.X. Wang, Y.X. Yue, J. Song, M. Chen, Y.Y. Wei, Q.P. Zhou, T. Dai, Y.H. Song,