Role of ATF4 in skeletal muscle atrophy

• Published in: Current opinion in clinical nutrition and metabolic care Vol. 20; no. 3; p. 164
• Main Authors: Adams, Christopher M, Ebert, Scott M, Dyle, Michael C
• Format: Journal Article
• Language: English
• Published: England 01.05.2017
• Subjects: Activating Transcription Factor 4 - metabolism; Aging - physiology; Animals; Fasting - physiology; Humans; Immobilization - physiology; Muscle Fibers, Skeletal - metabolism; Muscle, Skeletal - metabolism; Muscular Atrophy - etiology; Muscular Atrophy - genetics; Muscular Atrophy - physiopathology; Signal Transduction - genetics
• ISSN: 1473-6519
• DOI: 10.1097/MCO.0000000000000362

Here, we discuss recent work focused on the role of activating transcription factor 4 (ATF4) in skeletal muscle atrophy. Muscle atrophy involves and requires widespread changes in skeletal muscle gene expression; however, the transcriptional regulatory proteins responsible for those changes are not yet well defined. Recent work indicates that some forms of muscle atrophy require ATF4, a stress-inducible bZIP transcription factor subunit that helps to mediate a broad range of stress responses in mammalian cells. ATF4 expression in skeletal muscle fibers is sufficient to induce muscle fiber atrophy and required for muscle atrophy during several stress conditions, including aging, fasting, and limb immobilization. By helping to activate specific genes in muscle fibers, ATF4 contributes to the expression of numerous mRNAs, including at least two mRNAs (Gadd45a and p21) that encode mediators of muscle fiber atrophy. Gadd45a promotes muscle fiber atrophy by activating the protein kinase MEKK4. p21 promotes atrophy by reducing expression of spermine oxidase, a metabolic enzyme that helps to maintain muscle fiber size under nonstressed conditions. In skeletal muscle fibers, ATF4 is critical component of a complex and incompletely understood molecular signaling network that causes muscle atrophy during aging, fasting, and immobilization.