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J Appl Physiol 102: 1483-1489, 2007. First published January 4, 2007; doi:10.1152/japplphysiol.01147.2006
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STAT3 signaling is activated in human skeletal muscle following acute resistance exercise

Marissa K. Trenerry,1 Kate A. Carey,1 Alister C. Ward,2 and David Cameron-Smith1

1School of Exercise and Nutrition Science and 2School of Life and Environmental Sciences, Deakin University, Burwood, Victoria, Australia

Submitted 12 October 2006 ; accepted in final form 22 December 2006

The transcription factor signal transducer and activator of transcription 3 (STAT3) has been identified as a mediator of cytokine signaling and implicated in hypertrophy; however, the importance of this pathway following resistance exercise in human skeletal muscle has not been investigated. In the present study, the phosphorylation and nuclear localization of STAT3, together with STAT3-regulated genes, were measured in the early recovery period following intense resistance exercise. Muscle biopsy samples from healthy subjects (7 males, 23.0 + 0.9 yr) were harvested before and again at 2, 4, and 24 h into recovery following a single bout of maximal leg extension exercise (3 sets, 12 repetitions). Rapid and transient activation of phosphorylated (tyrosine 705) STAT3 was observed at 2 h postexercise. STAT3 phosphorylation paralleled the transient localization of STAT3 to the nucleus, which also peaked at 2 h postexercise. Downstream transcriptional events regulated by STAT3 activation peaked at 2 h postexercise, including early responsive genes c-FOS (800-fold), JUNB (38-fold), and c-MYC (140-fold) at 2 h postexercise. A delayed peak in VEGF (4-fold) was measured 4 h postexercise. Finally, genes associated with modulating STAT3 signaling were also increased following exercise, including the negative regulator SOCS3 (60-fold). Thus, following a single bout of intense resistance exercise, a rapid phosphorylation and nuclear translocation of STAT3 are evident in human skeletal muscle. These data suggest that STAT3 signaling is an important common element and may contribute to the remodeling and adaptation of skeletal muscle following resistance exercise.

signal transducer and activator of transcription-3; inflammation; regeneration; hypertrophy



Address for reprint requests and other correspondence: D. Cameron-Smith, School of Exercise and Nutrition Sciences, Deakin Univ., 221 Burwood Highway, Burwood, Victoria 3125, Australia (e-mail: david.cameron-smith{at}deakin.edu.au)




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[Abstract] [Full Text] [PDF]




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