mTOR signaling in skeletal muscle during sepsis and inflammation: Where does it all go wrong?

Robert A. Frost, Charles H. Lang

Research output: Contribution to journalReview article

70 Scopus citations

Abstract

The mammalian target of rapamycin (mTOR) is an evolutionarily conserved protein kinase that exquisitely regulates protein metabolism in skeletal muscle. mTOR integrates input from amino acids, growth factors, and intracellular cues to make or break muscle protein. mTOR accomplishes this task by stimulating the phosphorylation of substrates that control protein translation while simultaneously inhibiting proteasomal and autophagic protein degradation. In a metabolic twist of fate, sepsis induces muscle atrophy in part by the aberrant regulation of mTOR. In this review, we track the steps of normal mTOR signaling in muscle and examine where they go astray in sepsis and inflammation.

Original languageEnglish (US)
Pages (from-to)83-96
Number of pages14
JournalPhysiology
Volume26
Issue number2
DOIs
StatePublished - Apr 1 2011

All Science Journal Classification (ASJC) codes

  • Physiology

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