Protein kinase B/Akt: a nexus of growth factor and cytokine signaling in determining muscle mass

被引:141
作者
Frost, Robert A. [1 ]
Lang, Charles H. [1 ]
机构
[1] Penn State Univ, Coll Med, Dept Cellular & Mol Physiol, Hershey, PA 17033 USA
关键词
muscle metabolism; muscle cytokines; translation; hypertrophy; atrophy;
D O I
10.1152/japplphysiol.00089.2007
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Although the boundaries of skeletal muscle size are fundamentally determined by genetics, this dynamic tissue also demonstrates great plasticity in response to environmental and hormonal factors. Recent work indicates that contractile activity, nutrients, growth factors, and cytokines all contribute to determining muscle mass. Muscle responds not only to endocrine hormones but also to the autocrine production of growth factors and cytokines. Skeletal muscle synthesizes anabolic growth factors such as insulin-like growth factor (IGF)-I and potentially inhibitory cytokines such as interleukin (IL)-6, tumor necrosis factor (TNF)-alpha, and myostatin. These self-regulating inputs in turn influence muscle metabolism, including the use of nutrients such as glucose and amino acids. These changes are principally achieved by altering the activity of the protein kinase known as protein kinase B or Akt. Akt plays a central role in integrating anabolic and catabolic responses by transducing growth factor and cytokine signals via changes in the phosphorylation of its numerous substrates. Activation of Akt stimulates muscle hypertrophy and antagonizes the loss of muscle protein. Here we review the many signals that funnel through Akt to alter muscle mass.
引用
收藏
页码:378 / 387
页数:10
相关论文
共 118 条
[1]   Cardiac protection by mitoKATP channels is dependent on Akt translocation from cytosol to mitochondria during late preconditioning [J].
Ahmad, Nauman ;
Wang, Yigang ;
Haider, Khawaja Husnain ;
Wang, Boyu ;
Pasha, Zeeshan ;
Uzun, Oezge ;
Ashraf, Muhammad .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2006, 290 (06) :H2402-H2408
[2]   Selective activation of AMPK-PGC-1α or PKB-TSC2-mTOR signaling can explain specific adaptive responses to endurance or resistance training-like electrical muscle stimulation [J].
Atherton, PJ ;
Babraj, JA ;
Smith, K ;
Singh, J ;
Rennie, MJ ;
Wackerhage, H .
FASEB JOURNAL, 2005, 19 (02) :786-+
[3]   Insulin and amino-acid regulation of mTOR signaling and kinase activity through the Rheb GTPase [J].
Avruch, J. ;
Hara, K. ;
Lin, Y. ;
Liu, M. ;
Long, X. ;
Ortiz-Vega, S. ;
Yonezawa, K. .
ONCOGENE, 2006, 25 (48) :6361-6372
[4]   Signaling pathways in skeletal muscle remodeling [J].
Bassel-Duby, Rhonda ;
Olson, Eric N. .
ANNUAL REVIEW OF BIOCHEMISTRY, 2006, 75 :19-37
[5]   PML inhibits HIF-1α translation and neoangiogenesis through repression of mTOR [J].
Bernardi, Rosa ;
Guernah, Ilhem ;
Jin, David ;
Grisendi, Silvia ;
Alimonti, Andrea ;
Teruya-Feldstein, Julie ;
Cordon-Cardo, Carlos ;
Simon, M. Celeste ;
Rafii, Shahin ;
Pandolfi, Pier Paolo .
NATURE, 2006, 442 (7104) :779-785
[6]   AMP-activated protein kinase suppresses protein synthesis in rat skeletal muscle through down-regulated mammalian target of rapamycin (mTOR) signaling. [J].
Bolster, DR ;
Crozier, SJ ;
Kimball, SR ;
Jefferson, LS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (27) :23977-23980
[7]   Threonine 308 phosphorylated form of Akt translocates to the nucleus of PC12 cells under nerve growth factor stimulation and associates with the nuclear matrix protein nucleolin [J].
Borgatti, P ;
Martelli, AM ;
Tabellini, G ;
Bellacosa, A ;
Capitani, S ;
Neri, LM .
JOURNAL OF CELLULAR PHYSIOLOGY, 2003, 196 (01) :79-88
[8]   The role of IGFs in catabolism [J].
Botfield, C ;
Ross, RJM ;
Hinds, CJ .
BAILLIERES CLINICAL ENDOCRINOLOGY AND METABOLISM, 1997, 11 (04) :679-697
[9]   Localization of Rheb to the endomembrane is critical for its signaling function [J].
Buerger, Claudia ;
DeVries, Ben ;
Stambolic, Vuk .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2006, 344 (03) :869-880
[10]   IKKβ/NF-κB activation causes severe muscle wasting in mice [J].
Cai, DS ;
Frantz, JD ;
Tawa, NE ;
Melendez, PA ;
Oh, BC ;
Lidov, HGW ;
Hasselgren, PO ;
Frontera, WR ;
Lee, J ;
Glass, DJ ;
Shoelson, SE .
CELL, 2004, 119 (02) :285-298