Regulation of mTOR by mechanically induced signaling events in skeletal muscle

被引:66
作者
Hornberger, Troy Alan
Sukhija, Kunal Balu
Chien, Shu
机构
[1] Univ Calif San Diego, Dept Bioengn, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Whitaker Inst Biomed Engn, La Jolla, CA 92093 USA
关键词
amino acids; exercise; growth; hypertrophy; mechanotransduction; stretch; phosphatidic acid; phospholipase D; phosphotidylinositol-3-kinase (PI3K); rapamycin;
D O I
10.4161/cc.5.13.2921
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
Mechanical stimuli play a major role in the regulation of skeletal muscle mass, and the maintenance of muscle mass contributes significantly to disease prevention and the quality of life. Although a link between mechanical stimuli and the regulation of muscle mass has been recognized for decades, the mechanisms involved in converting mechanical information into the molecular events that control this process have not been defined. Nevertheless, significant advancements are being made in this field, and it has recently been established that signaling through a rapamycin-sensitive pathway is necessary for mechanically induced growth of skeletal muscle. Since rapamycin is a highly specific inhibitor of a protein kinase called the mammalian target of rapamycin ( mTOR), many investigators have concluded that mTOR signaling is necessary for the mechanically induced growth of skeletal muscle. In this review, we have summarized the current knowledge regarding how mechanical stimuli activate mTOR signaling, discussed the newly discovered role of phospholipase D (PLD) and phosphatidic acid (PA) in this pathway, and considered the potential roles of PLD and PA in the mechanical regulation of skeletal muscle mass.
引用
收藏
页码:1391 / 1396
页数:6
相关论文
共 77 条
[1]
mTOR pathway inhibition attenuates skeletal muscle growth induced by stretching [J].
Aoki, MS ;
Miyabara, EH ;
Soares, AG ;
Saito, ET ;
Moriscot, AS .
CELL AND TISSUE RESEARCH, 2006, 324 (01) :149-156
[2]
Regulation of glycogen synthesis by amino acids in cultured human muscle cells [J].
Armstrong, JL ;
Bonavaud, SM ;
Toole, BJ ;
Yeaman, SJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (02) :952-956
[3]
Phosphatidic acid, a key intermediate in lipid metabolism [J].
Athenstaedt, K ;
Daum, G .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1999, 266 (01) :1-16
[4]
Phosphorylation of p70S6k correlates with increased skeletal muscle mass following resistance exercise [J].
Baar, K ;
Esser, K .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1999, 276 (01) :C120-C127
[5]
Akt/mTOR pathway is a crucial regulator of skeletal muscle hypertrophy and can prevent muscle atrophy in vivo [J].
Bodine, SC ;
Stitt, TN ;
Gonzalez, M ;
Kline, WO ;
Stover, GL ;
Bauerlein, R ;
Zlotchenko, E ;
Scrimgeour, A ;
Lawrence, JC ;
Glass, DJ ;
Yancopoulos, GD .
NATURE CELL BIOLOGY, 2001, 3 (11) :1014-1019
[6]
Regulation of protein synthesis associated with skeletal muscle hypertrophy by insulin-, amino acid- and exercise-induced signalling [J].
Bolster, DR ;
Jefferson, LS ;
Kimball, SR .
PROCEEDINGS OF THE NUTRITION SOCIETY, 2004, 63 (02) :351-356
[7]
BOPPART MD, 2006, AM J PHYSL CELL PHYS
[8]
CONTROL OF P70 S6 KINASE BY KINASE-ACTIVITY OF FRAP IN-VIVO [J].
BROWN, EJ ;
BEAL, PA ;
KEITH, CT ;
CHEN, J ;
SHIN, TB ;
SCHREIBER, SL .
NATURE, 1995, 377 (6548) :441-446
[9]
RAFT1 phosphorylation of the translational regulators p70 S6 kinase and 4E-BP1 [J].
Burnett, PE ;
Barrow, RK ;
Cohen, NA ;
Snyder, SH ;
Sabatini, DM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (04) :1432-1437
[10]
Cass LA, 1999, MOL CELL BIOL, V19, P5882