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Am J Physiol Regul Integr Comp Physiol 290: R313-R321, 2006. First published September 8, 2005; doi:10.1152/ajpregu.00333.2005
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INFLAMMATION AND CYTOKINES

IGF-I stimulates protein synthesis in skeletal muscle through multiple signaling pathways during sepsis

Thomas C. Vary

Department of Cellular and Molecular Physiology, Penn State University College of Medicine, Hershey, Pennsylvania

Submitted 10 May 2005 ; accepted in final form 5 September 2005

Chronic septic abscess formation causes an inhibition of protein synthesis in gastrocnemius not observed in rats with a sterile abscess. Inhibition is associated with an impaired mRNA translation initiation that can be ameliorated by elevating IGF-I but not insulin. The present study investigated the ability of IGF-I signaling to stimulate protein synthesis in gastrocnemius by accelerating mRNA translation initiation. Experiments were performed in perfused hindlimb preparations from rats 5 days after induction of a septic abscess. Protein synthesis in gastrocnemius from septic rats was accelerated twofold by the addition of IGF-I (10 nM) to perfusate. IGF-I increased the phosphorylation of translation repressor 4E-binding protein-1 (4E-BP1). Hyperphosphorylation of 4E-BP1 in response to IGF-I resulted in its dissociation from the inactive eukaryotic initiation factor (eIF) 4E·4E-BP1 complex. Assembly of the active eIF4F complex (as assessed by the association eIF4G with eIF4E) was increased twofold by IGF-I in the perfusate. In addition, phosphorylation of eIF4G and ribosomal protein S6 kinase-1 (S6K1) was also enhanced by IGF-I. Activation of mammalian target of rapamycin, an upstream kinase implicated in phosphorylating both 4E-BP1 and S6K1, was also observed. Thus the ability of IGF-I to accelerate protein synthesis during sepsis may be related to a stimulation of signaling to multiple steps in translation initiation with an ensuing increased phosphorylation of eIF4G, eIF4E availability, and S6K1 phosphorylation.

messenger ribonuclease; translation initiation; eukaryotic initiation factors; eukaryotic initiation factor 4G; 4E-binding protein-1; eukaryotic initiation factor 4E; gastrocnemius; ribosomal protein S6 kinase-1



Address for reprint requests and other correspondence: T. C. Vary, Dept. of Cellular and Molecular Physiology, Rm. C4710, Penn State Univ. College of Medicine, H166, 500 Univ. Drive, Hershey, PA 17033 (e-mail:tvary{at}psu.edu)




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