SB431542 treatment promotes the hypertrophy of skeletal muscle fibers but decreases specific force

The small molecule inhibitor SB431542 inhibits activin type I receptors. The muscle growth‐inhibitor myostatin binds to and signals via these receptors. The aim of this study was to test the hypothesis that SB431542 can inhibit myostatin‐related Smad signaling and induce muscle growth in cultured C2...

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Published inMuscle & nerve Vol. 41; no. 5; pp. 624 - 629
Main Authors Watt, Kevin I., Jaspers, Richard T., Atherton, Phillip, Smith, Ken, Rennie, Michael J., Ratkevicius, Aivaras, Wackerhage, Henning
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.05.2010
Wiley
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Summary:The small molecule inhibitor SB431542 inhibits activin type I receptors. The muscle growth‐inhibitor myostatin binds to and signals via these receptors. The aim of this study was to test the hypothesis that SB431542 can inhibit myostatin‐related Smad signaling and induce muscle growth in cultured C2C12 myotubes and increase growth and specific force in cultured Xenopus muscle fibers. The effect of SB431542 was assessed in vitro on C2C12 myotubes and ex vivo using mature Xenopus muscle fibers. SB431542 treatment reduced myostatin‐induced C‐terminal Smad2 phosphorylation and resulted in the formation of enlarged myotubes. However myogenin expression was unchanged, while p70 S6k phosphorylation at Thr389, total myosin heavy chain, and the rate of protein synthesis were all reduced. Mature Xenopus muscle fibers that were treated with SB431542 had a higher fiber cross‐sectional area but decreased specific force production than control. SB431542 can initially antagonize myostatin signaling, but long‐term unexpected signaling effects occur. Muscle fibers hypertrophy, but their specific force decreases compared to control. Muscle Nerve, 2010
Bibliography:istex:C1A5E835326F323937D8F381C4BA162E1A72302C
ArticleID:MUS21573
ark:/67375/WNG-M51NNRJR-X
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0148-639X
1097-4598
DOI:10.1002/mus.21573