Heart failure is an increasingly prevalent disease syndrome with a poor long-term prognosis. As a result of progressive myocardial dysfunction, the adrenergic nervous system and the renin-angiotensin system are abnormally activated. One consequence of persistently elevated adrenergic drive is the activation of multiple compensatory physiological and cellular mechanisms producing down-regulation and desensitization of the myocardial beta-adrenergic receptor (AR) pathways. To investigate the mechanisms involved in beta-AR down-regulation, my previous work, and that of others, has focused on measuring the abundance of mRNAs encoding beta1- and beta2-ARs. Although mechanisms responsible for regulation of adrenergic receptor mRNAs have not been investigated extensively, it is becoming increasingly clear that analogous to protooncogenes and cytokines, up- and down-regulation of beta-AR mRNAs by stabilization/destabilization of the mRNA may be an important regulatory control point. Yet, only very preliminary data exist for the relationship between mRNA stability and any component of the G-protein linked receptor pathways. Recently, we have found that beta-AR mRNA interacts with an Mr 35,000 protein. This protein shares several important characteristics with other mRNA binding proteins that preferentially interact with AU-rich regions, and have been shown to be involved in the targeting of mRNA for rapid turnover. More importantly, the apparent abundance of this mRNA binding protein is highly regulated, being increased by stimulation of pathways that down-regulate beta-AR and decreased by stimulation of pathways that up-regulate or uncouple beta-AR. The essence of this proposal is to begin to explore, in depth, the cellular mechanisms by which adrenergic receptor mRNA abundance is controlled by the process of mRNA stability. To perform this objective, I will focus on: domain specificity of beta-AR mRNA binding proteins, map regions of beta-AR mRNA which may act as stabilizing or destabilizing elements, determine the effect of the extent of polyadenylation on beta-AR mRNA stability, develop a cell-free, in vitro, mRNA decay system, and begin to purify and characterize mRNA binding proteins that bind to beta- AR mRNA. The results of these studies should extend our knowledge in two important areas. First, understanding in greater detail the mechanisms of regulation of beta-AR mRNA stability will help more clearly define a major phenotype of heart failure at a molecular level. Second, what can be learned from beta-AR model systems often serves as a basis for extension to other G- protein coupled receptors.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
First Independent Research Support & Transition (FIRST) Awards (R29)
Project #
5R29HL051239-02
Application #
2227868
Study Section
Pharmacology A Study Section (PHRA)
Project Start
1994-01-01
Project End
1998-12-31
Budget Start
1995-01-01
Budget End
1995-12-31
Support Year
2
Fiscal Year
1995
Total Cost
Indirect Cost
Name
University of Colorado Denver
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
065391526
City
Aurora
State
CO
Country
United States
Zip Code
80045
Port, J David; Walker, Lori A; Polk, Jeremy et al. (2011) Temporal expression of miRNAs and mRNAs in a mouse model of myocardial infarction. Physiol Genomics 43:1087-95
Dockstader, Karen; Nunley, Karin; Karimpour-Fard, Anis et al. (2011) Temporal analysis of mRNA and miRNA expression in transgenic mice overexpressing Arg- and Gly389 polymorphic variants of the ?1-adrenergic receptor. Physiol Genomics 43:1294-306
David Gerecht, Pamela S; Taylor, Molly A; Port, J David (2010) Intracellular localization and interaction of mRNA binding proteins as detected by FRET. BMC Cell Biol 11:69
Port, J David; Sucharov, Carmen (2010) Role of microRNAs in cardiovascular disease: therapeutic challenges and potentials. J Cardiovasc Pharmacol 56:444-53