Cellular and molecular pathways controlling muscle size in response to exercise

被引:28
作者
Attwaters, Michael [1 ]
Hughes, Simon M. [1 ]
机构
[1] Kings Coll London, Randall Ctr Cell & Mol Biophys, Sch Basic & Med Biosci, London SE1 1UL, England
基金
英国医学研究理事会;
关键词
calcium; energy; exercise; force; growth; hypertrophy; muscle; PROTEIN-KINASE-C; DEPENDENT TRANSCRIPTIONAL PATHWAY; CILIARY NEUROTROPHIC FACTOR; SKELETAL-MUSCLE; RESISTANCE EXERCISE; SATELLITE CELL; MAMMALIAN TARGET; SIGNALING PATHWAYS; FIBER HYPERTROPHY; GENE-EXPRESSION;
D O I
10.1111/febs.15820
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
From the discovery of ATP and motor proteins to synaptic neurotransmitters and growth factor control of cell differentiation, skeletal muscle has provided an extreme model system in which to understand aspects of tissue function. Muscle is one of the few tissues that can undergo both increase and decrease in size during everyday life. Muscle size depends on its contractile activity, but the precise cellular and molecular pathway(s) by which the activity stimulus influences muscle size and strength remain unclear. Four correlates of muscle contraction could, in theory, regulate muscle growth: nerve-derived signals, cytoplasmic calcium dynamics, the rate of ATP consumption and physical force. Here, we summarise the evidence for and against each stimulus and what is known or remains unclear concerning their molecular signal transduction pathways and cellular effects. Skeletal muscle can grow in three ways, by generation of new syncytial fibres, addition of nuclei from muscle stem cells to existing fibres or increase in cytoplasmic volume/nucleus. Evidence suggests the latter two processes contribute to exercise-induced growth. Fibre growth requires increase in sarcolemmal surface area and cytoplasmic volume at different rates. It has long been known that high-force exercise is a particularly effective growth stimulus, but how this stimulus is sensed and drives coordinated growth that is appropriately scaled across organelles remains a mystery.
引用
收藏
页码:1428 / 1456
页数:29
相关论文
共 304 条
[1]   Muscle size and strength are increased following walk training with restricted venous blood flow from the leg muscle, Kaatsu-walk training [J].
Abe, T ;
Kearns, CF ;
Sato, Y .
JOURNAL OF APPLIED PHYSIOLOGY, 2006, 100 (05) :1460-1466
[2]   Diacylglycerol kinase-ζ localization in skeletal muscle is regulated by phosphorylation and interaction with syntrophins [J].
Abramovici, H ;
Hogan, AB ;
Obagi, C ;
Topham, MK ;
Gee, SH .
MOLECULAR BIOLOGY OF THE CELL, 2003, 14 (11) :4499-4511
[3]   The relationships among IGF-1, DNA content, and protein accumulation during skeletal muscle hypertrophy [J].
Adams, GR ;
Haddad, F .
JOURNAL OF APPLIED PHYSIOLOGY, 1996, 81 (06) :2509-2516
[4]  
Adrian ED, 1929, J PHYSIOL-LONDON, V67, P119
[5]  
ALFORD E, 1987, J APPL PHYSIOL, V96, P635
[6]   Skeletal muscle fatigue: Cellular mechanisms [J].
Allen, D. G. ;
Lamb, G. D. ;
Westerblad, H. .
PHYSIOLOGICAL REVIEWS, 2008, 88 (01) :287-332
[7]   REGIONALIZED ADAPTATIONS AND MUSCLE-FIBER PROLIFERATION IN STRETCH-INDUCED ENLARGEMENT [J].
ALWAY, SE ;
WINCHESTER, PK ;
DAVIS, ME ;
GONYEA, WJ .
JOURNAL OF APPLIED PHYSIOLOGY, 1989, 66 (02) :771-781
[8]   Down-Regulation of Akt/Mammalian Target of Rapamycin Signaling Pathway in Response to Myostatin Overexpression in Skeletal Muscle [J].
Amirouche, Adel ;
Durieux, Anne-Cecile ;
Banzet, Sebastien ;
Koulmann, Nathalie ;
Bonnefoy, Regis ;
Mouret, Catherine ;
Bigard, Xavier ;
Peinnequin, Andre ;
Freyssenet, Damien .
ENDOCRINOLOGY, 2009, 150 (01) :286-294
[9]   Lack of myostatin results in excessive muscle growth but impaired force generation [J].
Amthor, Helge ;
Macharia, Raymond ;
Navarrete, Roberto ;
Schuelke, Markus ;
Brown, Susan C. ;
Otto, Anthony ;
Voit, Thomas ;
Muntoni, Francesco ;
Vrbova, Gerta ;
Partridge, Terence ;
Zammit, Peter ;
Bunger, Lutz ;
Patel, Ketan .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (06) :1835-1840
[10]  
ANJANA R, 1997, CELL, V15, P707