NF-kappaB-induced loss of MyoD messenger RNA: possible role in muscle decay and cachexia
- PMID: 11009425
- DOI: 10.1126/science.289.5488.2363
NF-kappaB-induced loss of MyoD messenger RNA: possible role in muscle decay and cachexia
Abstract
MyoD regulates skeletal muscle differentiation (SMD) and is essential for repair of damaged tissue. The transcription factor nuclear factor kappa B (NF-kappaB) is activated by the cytokine tumor necrosis factor (TNF), a mediator of skeletal muscle wasting in cachexia. Here, the role of NF-kappaB in cytokine-induced muscle degeneration was explored. In differentiating C2C12 myocytes, TNF-induced activation of NF-kappaB inhibited SMD by suppressing MyoD mRNA at the posttranscriptional level. In contrast, in differentiated myotubes, TNF plus interferon-gamma (IFN-gamma) signaling was required for NF-kappaB-dependent down-regulation of MyoD and dysfunction of skeletal myofibers. MyoD mRNA was also down-regulated by TNF and IFN-gamma expression in mouse muscle in vivo. These data elucidate a possible mechanism that may underlie the skeletal muscle decay in cachexia.
Comment in
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Biomedicine. Protein loss in cancer cachexia.Science. 2000 Sep 29;289(5488):2293-4. doi: 10.1126/science.289.5488.2293. Science. 2000. PMID: 11041796 No abstract available.
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