Myf 5 and MyoD play critical roles in the specification and/or maintenance of muscle progenitor cells during development. While """"""""knock out"""""""" mice provide a valuable tool for determining which functions of these factors are unique and the extent to which they might overlap, that Myf 5 null mice die at birth has limited the study of the maturation and regeneration of Myf 5 null muscles. By transplanting newborn Myf 5 null extensor digitorum longus (EDL) muscles into the bed of normal hosts (where these muscle regenerate and become innervated), we can compare these processes in Myf 5 and MyoD null mice. MyoD null muscles exhibits a regeneration deficit involving an inhibition of its satellite cells ability to undergo terminal differentiation; whereas, it is suggested that Myf 5 null myoblasts undergo precocious differentiation. Comparative studies of Myf 5 null, MyoD null and wild type muscle regeneration will be carried out with EM and morphometric analyses. The effect of the absence of Myf 5 on the number of satellite cell, satellite cell activation, proliferation and terminal differentiation will be assessed in regenerating muscle and in vitro. The effects of the absence of Myf 5 on muscle gene expression (e.g., genes encoding the MRFs, M cadhedrin, desmin, c met tyrosine kinase, etc.) in regenerating muscles and in cultures of myosatellite cells will be evaluated with competitive PCR and immunohistochemistry. Comparisons will be made with similar studies of normal and MyoD null regenerating muscle (Sabourin et al., 1999). The effect of the absence of Myf 5 on muscle phenotype will be evaluated with immunohistochemistry and gel electrophoresis. Muscle diseases are characterized by degeneration regeneration, with the regenerative effort being insufficient to keep pace with degeneration. These studies should provide clues to how it may be possible to increase muscle's regenerative response.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Research Project (R01)
Project #
5R01AR046479-03
Application #
6534490
Study Section
Cell Development and Function Integrated Review Group (CDF)
Program Officer
Lymn, Richard W
Project Start
2000-09-01
Project End
2005-08-31
Budget Start
2002-09-01
Budget End
2003-08-31
Support Year
3
Fiscal Year
2002
Total Cost
$274,115
Indirect Cost
Name
University of Pittsburgh
Department
Physiology
Type
Schools of Medicine
DUNS #
053785812
City
Pittsburgh
State
PA
Country
United States
Zip Code
15213
Washabaugh, Charles H; Ontell, Martin P; Shand, Stuart H et al. (2007) Neuronal control of myogenic regulatory factor accumulation in fetal muscle. Dev Dyn 236:732-45
Washabaugh, C H; Ontell, M P; Ontell, M (2004) Nonmuscle stem cells fail to significantly contribute to regeneration of normal muscle. Gene Ther 11:1724-8
Wang, Zuo-Zhong; Washabaugh, Charles H; Yao, Yun et al. (2003) Aberrant development of motor axons and neuromuscular synapses in MyoD-null mice. J Neurosci 23:5161-9
Washabaugh, C H; Ontell, M P; Kant, J A et al. (2001) Effect of chronic denervation and denervation-reinnervation on cytoplasmic creatine kinase transcript accumulation. J Neurobiol 47:194-206