4.8 Article

TNFα inhibits skeletal myogenesis through a PW1-dependent pathway by recruitment of caspase pathways

Journal

EMBO JOURNAL
Volume 21, Issue 4, Pages 631-642

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/emboj/21.4.631

Keywords

bax; cachexia; caspase; Peg3; TNF alpha

Funding

  1. NCI NIH HHS [P01-CA-80058-01A1, P01 CA080058] Funding Source: Medline
  2. NICHD NIH HHS [T32 HD 07478, T32 HD007478] Funding Source: Medline

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Cachexia is associated with poor prognosis in patients with chronic disease. Tumor necrosis factor-alpha (TNFalpha) plays a pivotal role in mediating cachexia and has been demonstrated to inhibit skeletal muscle differentiation in vitro. It has been proposed that TNFalpha-mediated activation of NFkappaB leads to down regulation of MyoD, however the mechanisms underlying TNFalpha effects on skeletal muscle remain poorly understood. We report here a novel pathway by which TNFalpha inhibits muscle differentiation through activation of caspases in the absence of apoptosis. TNFalpha-mediated caspase activation and block of differentiation are dependent upon the expression of PW1, but occur independently of NFkappaB activation. PW1 has been implicated previously in p53-mediated cell death and can induce bax translocation to the mitochondria. We show that bax-deficient myoblasts do not activate caspases and differentiate in the presence of TNFalpha, highlighting a role for bax-dependent caspase activation in mediating TNFalpha effects. Taken together, our data reveal that TNFalpha inhibits myogenesis by recruiting components of apoptotic pathways through PW1.

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