Studies will be directed toward learning more about the factors that regulate cardiac protein balance, using fetal mouse hearts in organ culture as the experimental model. The importance of changes in protein degradation as well as protein synthesis will be explored. The cellular mechanisms responsible for protein degradation will be studied, with special emphasis on the possible roles of the lysosomal apparatus and the microtubular apparatus of the cell. In recognition that the mechanisms and regulation of protein balance may be different for different proteins, attention will be focused on the separate assessment of changes in the synthesis and degradation of individual proteins (e.g., myosin) or classes of protein (e.g., organellar vs. cytosolic) during various interventions. Specific studies will include those designed to explore the effects of agents that disrupt the microtubular apparatus; lysosomotropic agents and proteinase inhibitors; hormones; and certain pharmacological agents. Other experiments will be concerned with the role of autophagic vacuole formation in the repair of sublethal cell injury and the changes in protein turnover that accompany this phenomenon. In all studies, correlations will be made between changes in net protein balance, the synthesis and degradation of total protein and of different subclasses of protein, and lysosomal properties as assessed biochemically and anatomically.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL014706-14
Application #
3334838
Study Section
Cardiovascular Study Section (CVA)
Project Start
1977-01-01
Project End
1986-12-31
Budget Start
1985-01-01
Budget End
1985-12-31
Support Year
14
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of Texas Sw Medical Center Dallas
Department
Type
Overall Medical
DUNS #
City
Dallas
State
TX
Country
United States
Zip Code
75390
Ridout, R M; Wildenthal, K; Decker, R S (1986) Lysosomal responses of fetal mouse hearts recovering from anoxia and substrate depletion. J Mol Cell Cardiol 18:853-65
Ridout, R M; Wildenthal, K; Decker, R S (1986) Influence of agents that alter lysosomal function on fetal mouse hearts recovering from anoxia and substrate depletion. J Mol Cell Cardiol 18:867-76
Clark, A F; Wildenthal, K (1986) Disproportionate reduction of actin synthesis in hearts of starved rats. J Biol Chem 261:13168-72
Wildenthal, K; Wakeland, J R (1985) The role of lysosomes in the degradation of myofibrillar and non-myofibrillar proteins in heart. Prog Clin Biol Res 180:511-20
Wildenthal, K; Crie, J S; Ord, J M et al. (1985) The role of lysosomes and microtubules in cardiac protein degradation. Adv Myocardiol 5:137-44