| Literature DB >> 25686491 |
Q Zhao1, S T Yang1, J J Wang2, J Zhou3, S S Xing1, C C Shen1, X X Wang1, Y X Yue1, J Song1, M Chen1, Y Y Wei1, Q P Zhou1, T Dai1, Y H Song4.
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.Entities:
Keywords: C2C12; IGF-1; TNF-α
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Year: 2015 PMID: 25686491 DOI: 10.1016/j.bbrc.2015.02.026
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575