Senile muscle atrophy represents one of the major problems associated with aging and is characterized by loss of strength and muscle mass. These changes ultimately restrict mobility and, consequently, the independence of a growing segment of our society. The proposed research will probe cellular and molecular changes occurring in skeletal muscle during aging. These experiments will focus on the in vitro activity of skeletal muscle satellite cells, the cells responsible for muscle hypertrophy and regeneration. Satellite cells are muscle precursor cells that exist in postnatal muscle and have the ability to divide, differentiate and add new nuclei to existing fibers durng hypertrophy. They also have the ability to form entirely new fibers during regeneration. Because of the importance of these cells in muscle hypertrophy, the diminished capacity of satellite cells in old muscle to respond to normal physiological signals could play a major role in the inability of muscle in older individuals to maintain mass. In the proposed experiments, donor rats from three age groups, young, adult and old, will be used to investigate changes in the proliferative activity of satellite cells in response to a somatomedin-like protein, multiplication stimulating activity (MSA). In addition, age-related changes in the interaction of this hormone with satellite cells will be investigated by determining the affinity of MSA receptors on satellite cells for MSA, the number of receptors present per cell and the rate of internalization of the hormone receptor complex. This research program is designed to provide fundamental insights into the cellular and molecular mechanisms of muscle aging with the ultimate goal of contributing toward the alleviation of problems associated with senile muscle atrophy.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Project (R01)
Project #
5R01AG003393-04
Application #
3114712
Study Section
Pathobiochemistry Study Section (PBC)
Project Start
1982-05-01
Project End
1986-04-30
Budget Start
1985-05-01
Budget End
1986-04-30
Support Year
4
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of Arizona
Department
Type
Earth Sciences/Resources
DUNS #
City
Tucson
State
AZ
Country
United States
Zip Code
85722
Kumamoto, T; Kleese, W C; Cong, J Y et al. (1992) Localization of the Ca(2+)-dependent proteinases and their inhibitor in normal, fasted, and denervated rat skeletal muscle. Anat Rec 232:60-77
Allen, R E; Rankin, L L; Greene, E A et al. (1991) Desmin is present in proliferating rat muscle satellite cells but not in bovine muscle satellite cells. J Cell Physiol 149:525-35
Greene, E A; Allen, R E (1991) Growth factor regulation of bovine satellite cell growth in vitro. J Anim Sci 69:146-52
Allen, R E; Rankin, L L (1990) Regulation of satellite cells during skeletal muscle growth and development. Proc Soc Exp Biol Med 194:81-6
Johnson, S E; Allen, R E (1990) The effects of bFGF, IGF-I, and TGF-beta on RMo skeletal muscle cell proliferation and differentiation. Exp Cell Res 187:250-4
Allen, R E; Boxhorn, L K (1989) Regulation of skeletal muscle satellite cell proliferation and differentiation by transforming growth factor-beta, insulin-like growth factor I, and fibroblast growth factor. J Cell Physiol 138:311-5
Ito, M; Pierce, P R; Allen, R E et al. (1989) Effect of monoclonal antibodies on the properties of smooth muscle myosin. Biochemistry 28:5567-72
Thompson, S H; Boxhorn, L K; Kong, W Y et al. (1989) Trenbolone alters the responsiveness of skeletal muscle satellite cells to fibroblast growth factor and insulin-like growth factor I. Endocrinology 124:2110-7
Dodson, M V; Allen, R E; Shimizu, N et al. (1987) Interaction of ovine somatomedin and multiplication stimulating activity/rat insulin-like growth factor II with cultured skeletal muscle satellite cells. Acta Endocrinol (Copenh) 116:425-32
Allen, R E; Boxhorn, L K (1987) Inhibition of skeletal muscle satellite cell differentiation by transforming growth factor-beta. J Cell Physiol 133:567-72

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