Exercise-Induced Activation of STAT3 Signaling Is Increased with Age
Author(s) -
Marissa K. Trenerry,
Kate A. Carey,
Alister C. Ward,
Michelle M. Farnfield,
David CameronSmith
Publication year - 2008
Publication title -
rejuvenation research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.872
H-Index - 60
eISSN - 1557-8577
pISSN - 1549-1684
DOI - 10.1089/rej.2007.0643
Subject(s) - socs3 , stat3 , skeletal muscle , proinflammatory cytokine , endocrinology , signal transduction , medicine , junb , biology , transcription factor , cytokine , interleukin 6 , stat protein , microbiology and biotechnology , inflammation , gene , biochemistry
Activation of the transcription factor signal transducers and activators of transcription (STAT) 3 is common to many inflammatory cytokines and growth factors, with recent evidence of involvement in skeletal muscle regeneration. The purpose of this study was to determine whether STAT3 signaling activation is regulated differentially, at rest and following intense resistance exercise, in aged human skeletal muscle. Skeletal muscle biopsies were harvested from healthy younger (n = 11, 20.4 +/- 0.8 years) and older men (n = 10, 67.4 +/- 1.3 years) under resting conditions and 2 h after the completion of resistance exercise. No differences were evident at rest, whereas the phosphorylation of STAT3 was significantly increased in old (23-fold) compared to young (5-fold) subjects after exercise. This correlated with significantly higher induction of the STAT3 target genes including; interleukin-6 (IL-6), JUNB, c-MYC, and suppressor of cytokine signaling (SOCS) 3 mRNA in older subjects following exercise. Despite increased SOCS3 mRNA, cellular protein abundance was suppressed. SOCS3 protein is an important negative regulator of STAT3 activation and cytokine signaling. Thus, in aged human muscle, elevated responsiveness of the STAT3 signaling pathway and suppressed SOCS3 protein are evident following resistance exercise. These data suggest that enhanced STAT3 signaling responsiveness to proinflammatory factors may impact on mechanisms of muscle repair and regeneration.
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