It has been known for many years that high resistance exercise results in the hypertrophy of skeletal muscle, however, to date very little is known about the signaling mechanisms regulating this growth response. Studies of exercise-induced hypertrophy in mammals have shown that an early response to one bout of exercise is a transient increase in protein synthesis followed by subsequent increases in muscle specific mRNAs. This pattern of change suggests a model in which the transient increase in protein synthesis produces specific factors important for muscle growth. The overall aims of this project are to elucidate the upstream signaling mechanism(s) necessary for protein synthesis changes following resistance exercise and to determine the role of translational activation in the development of skeletal muscle hypertrophy. We have modified an in vivo model to study the regulation of exercise-stimulated protein synthesis. With this model, the phosphorylation of p70s6k was identified a an acute marker of the hypertrophic growth response. This provides a critical starting point from which experiments have been designed to delineate the growth- related signaling pathways stimulated by exercise. We also have found that p70s6k is activated following stretch-induced growth of myotubes in vitro. The experiments proposed rely on the use of in vitro stretch system to screen for the critical factors and pathways activated. These factors and pathways will subsequently be tested for their physiological significance in vivo. The findings from this project are important for the basic understanding of how striated muscle cells regulate their size in response to increased loading. In addition, the results from these studies have tremendous application for the fields of aging and rehabilitation. Age-associated muscle atrophy is a debilitating condition that can decrease the quality of life as well as limit independent living for the elderly. Understanding the factors and pathways that regulate the growth response of skeletal muscle will be important for designing therapeutic treatments (pharmacological or exercise based) to attenuate or reverse losses in muscle mass.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Research Project (R01)
Project #
5R01AR045617-02
Application #
6149719
Study Section
Respiratory and Applied Physiology Study Section (RAP)
Program Officer
Lymn, Richard W
Project Start
1999-02-05
Project End
2004-01-31
Budget Start
2000-02-01
Budget End
2001-01-31
Support Year
2
Fiscal Year
2000
Total Cost
$220,002
Indirect Cost
Name
University of Illinois at Chicago
Department
Nutrition
Type
Schools of Allied Health Profes
DUNS #
121911077
City
Chicago
State
IL
Country
United States
Zip Code
60612
Chaillou, Thomas; Jackson, Janna R; England, Jonathan H et al. (2015) Identification of a conserved set of upregulated genes in mouse skeletal muscle hypertrophy and regrowth. J Appl Physiol (1985) 118:86-97
Chaillou, Thomas; Lee, Jonah D; England, Jonathan H et al. (2013) Time course of gene expression during mouse skeletal muscle hypertrophy. J Appl Physiol (1985) 115:1065-74
Srikuea, Ratchakrit; Zhang, Xiping; Park-Sarge, Ok-Kyong et al. (2012) VDR and CYP27B1 are expressed in C2C12 cells and regenerating skeletal muscle: potential role in suppression of myoblast proliferation. Am J Physiol Cell Physiol 303:C396-405
Drummond, Micah J; McCarthy, John J; Sinha, Mala et al. (2011) Aging and microRNA expression in human skeletal muscle: a microarray and bioinformatics analysis. Physiol Genomics 43:595-603
Miyazaki, Mitsunori; McCarthy, John J; Fedele, Mark J et al. (2011) Early activation of mTORC1 signalling in response to mechanical overload is independent of phosphoinositide 3-kinase/Akt signalling. J Physiol 589:1831-46
McCarthy, John J; Mula, Jyothi; Miyazaki, Mitsunori et al. (2011) Effective fiber hypertrophy in satellite cell-depleted skeletal muscle. Development 138:3657-66
Mavalli, Mahendra D; DiGirolamo, Douglas J; Fan, Yong et al. (2010) Distinct growth hormone receptor signaling modes regulate skeletal muscle development and insulin sensitivity in mice. J Clin Invest 120:4007-20
McCarthy, John J; Esser, Karyn A (2010) Anabolic and catabolic pathways regulating skeletal muscle mass. Curr Opin Clin Nutr Metab Care 13:230-5
Esser, Karyn A; McCarthy, John J; Miyazaki, Mitsunori (2010) Comments on Point:Counterpoint: IGF is/is not the major physiological regulator of muscle mass. IGF-1 is not key for adult skeletal muscle hypertrophy. J Appl Physiol 108:1830
Miyazaki, Mitsunori; McCarthy, John J; Esser, Karyn A (2010) Insulin like growth factor-1-induced phosphorylation and altered distribution of tuberous sclerosis complex (TSC)1/TSC2 in C2C12 myotubes. FEBS J 277:2180-91

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