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Role of mitochondria-associated spaces in the regulation of compartmentation of cAMP signaling

线粒体相关空间在 cAMP 信号传导调节中的作用

基本信息

批准号：
10077909
负责人：
Shailesh Agarwal
金额：
$ 20.77万
依托单位：
UNIVERSITY OF NEVADA RENO
依托单位国家：
美国
项目类别：
财政年份：
2019
资助国家：
美国
起止时间：
2019-01-01 至 2023-12-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/10077909
关键词：
A kinase anchoring protein Adopted Affect Anatomy Arrhythmia Biosensor Buffers Cardiac Cardiac Myocytes Cardiovascular Diseases Cardiovascular Physiology Cardiovascular system Cell Volumes Cells Centers of Research Excellence Computer Models Computing Methodologies Confocal Microscopy Cyclic AMP Cyclic AMP-Dependent Protein Kinases Cytoskeletal Proteins Cytosol Development Diffuse Diffusion Disease Enzymes Event Fluorescence Resonance Energy Transfer G-Protein-Coupled Receptors Goals Health Heart Heart Diseases Heart Hypertrophy Heart failure Human Hypertrophy Image Individual Lead Link Location Mathematics Measures Mediating Membrane Membrane Microdomains Microtubules Mitochondria Molecular Morphology Movement Muscle Cells Myofibrils Nevada Organelles Outcome Play Positioning Attribute Process Production Prostaglandin Receptor Protein Sortings Proteins Regulation Role Sarcoplasmic Reticulum Second Messenger Systems Signal Transduction Spectrum Analysis Structure Study models Subcellular Spaces Techniques Testing Therapeutic Ventricular base beta-adrenergic receptor computer studies enzyme activity glucose-regulated proteins heart function knock-down mathematical model muscle LIM protein novel therapeutic intervention overexpression patch clamp phosphoric diester hydrolase prevent protein expression receptor response segregation small hairpin RNA solute

项目摘要

Project Summary Various G-protein-coupled receptors elicit distinct functional responses within a cell, even though they use the common diffusible second messenger cAMP. For instance, while stimulation of either β-adrenergic receptors or E-type prostaglandin receptors leads to cAMP production, only β-adrenergic receptors regulate cardiac myocyte contractility. The ability of a cell to distinguish between cAMP produced in the same cell can only be explained if engagement of different receptors generates distinct receptor-specific pools of cAMP. However, the underlying mechanisms responsible for creating compartmentalized cAMP are not completely understood. Compartmentalized cAMP signaling regulates cardiac contractility and thus is essential for normal functioning of the heart. Consistent with this, dysregulation of cAMP compartmentalization has been linked to several cardiovascular diseases, including cardiac arrhythmias, hypertrophy, and heart failure. Most previous studies have focused on activities of phosphodiesterases, the enzymes that breakdown cAMP, to explain cAMP compartmentation. However, several mathematical studies have predicted that PDE activity alone is not sufficient. These studies have suggested that the mobility of cAMP must be slower than free diffusion to prevent cAMP from reaching non-specific target proteins. We have recently demonstrated that the intracellular mobility of cAMP is markedly hampered by buffering mediated by mitochondria-associated protein kinase A. Now, a new computational study has predicted that, in addition to slow diffusion of cAMP, anatomically restricted spaces within a cell are key to hindering cAMP movement. In cardiac myocytes, mitochondria occupy 30% of the cell volume and are associated with constrained spaces through interactions with the sarcoplasmic reticulum and cytoskeletal proteins. The overall aim of this proposal is to explore the concept that the tight spaces associated with mitochondria regulate cAMP compartmentation. The tethering of mitochondria to the sarcoplasmic reticulum by the proteins, mitofusin-2 (MFN2), glucose-regulated protein 75 (GRP75), and phosphofurin acidic cluster sorting protein 2 (PACS2), creates tight spaces between these organelles. In the FIRST AIM of this study, we will test the hypothesis that the anatomically restricted spaces between mitochondria and the sarcoplasmic reticulum hinder cAMP movement and contribute to cAMP compartmentation. In cardiac myocytes, mitochondrial arrangement is regulated by microtubules and muscle LIM protein (MLP). Disruption of microtubules or MLP causes disorganization of mitochondria and alters mitochondrial morphology, thereby changing the cytosolic spaces associated with mitochondria. Thus, in the SECOND AIM, we hypothesize that cAMP compartmentation is hampered following mitochondrial derangement in microtubule-disrupted cells. To test these hypotheses, we adopt multipronged and complementary approaches to study cAMP compartmentation. Using a variety of advanced techniques, we will measure cAMP mobility, changes in cAMP levels within specific intracellular locations, changes in Ca2+ channel currents and intracellular Ca2+ transients, and test changes in functional responses, such as cell shortening, following stimulation of individual receptors. The goal of this proposal is to elucidate the fundamental mechanisms responsible for facilitating cAMP compartmentation. We believe that this approach may ultimately lead to the development of potential therapeutic strategies to overcome the burden of cardiac diseases.

项目总结