The sinoatrial node (SAN), located in the right atrium, serves as the natural cardiac pacemaker and is responsible for initiating each normal heartbeat. SAN dysfunction, characterized by slow and/or irregular pacemaker activity, is common in cardiovascular disease and in the aging population and is a major indicator for cardiac pacemaker implantation. While defects in activity of multiple ion channels have been linked to abnormal SAN cell membrane excitability and SAN dysfunction, little is known about molecular pathways responsible for ion channel membrane targeting. Recent studies from our group have identified a novel role for the actin-associated polypeptide BetaIV spectrin in organizing local signaling domains for membrane ion channels in ventricular myocytes. However, the pathways responsible for organization of analogous domains in SAN cells remain largely unstudied. There is a need to elucidate the mechanisms by which ion channel membrane domains are coordinated to regulate cardiac pacemaking. The objective of this proposal is to define the role of the actin-associated polypeptide Beta-IV spectrin in ion channel targeting and regulation of membrane excitability in SAN cells, and to develop quantitative tools for analysis of SAN cell behavior and susceptibility to dysfunction. My central hypothesis is that Beta-IV spectrin determines normal membrane localization of the mechanosensitive background K+ channel TREK-1 to control SAN cell membrane excitability. Furthermore, I hypothesize that disruption of the Beta-IV spectrin/TREK-1 complex at the sinoatrial node membrane promotes abnormal cell membrane excitability and sinus node dysfunction. My hypotheses will be tested using an innovative combination of experimental and mathematical modeling techniques. I believe that the findings from these studies will identify a pathway for targeting TREK-1 to the sinoatrial node membrane, will develop new analytical/mathematical tools to understand SAN function, and will generate new directions for future research of cell excitability and cardiac pacemaking in normal and diseased hearts.

Public Health Relevance

The normal heartbeat (sinus rhythm) begins with an electrical impulse generated by the sinoatrial node, a specialized collection of cells located in the right atrium. Sinoatrial node dysfunction, results in irregular pacemaking and is a high indicator for permanent cardiac pacemaker implantation. This research seeks to discover the role of beta-IV spectrin, an actin-associated polypeptide, in control of normal cardiac pacemaking through membrane targeting of a recently discovered mechanosensitive background K+ channel, TREK-1. These studies will combine original experiments with novel quantitative analyses to determine the contribution of the spectrin/TREK-1 complex to sinoatrial node dysfunction. We anticipate that results from this study will uncover a novel molecular pathway for control of pacemaking and cell membrane excitability in the sinoatrial node, and will potentially identify new therapeuti targets for human heart disease patients with sinoatrial node dysfunction.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
1F31HL129766-01
Application #
8982512
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Meadows, Tawanna
Project Start
2015-08-17
Project End
2017-08-16
Budget Start
2015-08-17
Budget End
2016-08-16
Support Year
1
Fiscal Year
2015
Total Cost
Indirect Cost
Name
Ohio State University
Department
Engineering (All Types)
Type
Biomed Engr/Col Engr/Engr Sta
DUNS #
832127323
City
Columbus
State
OH
Country
United States
Zip Code
43210
Onal, Birce; Hund, Thomas J (2017) Integrative approaches for prediction of cardiotoxic drug effects and mitigation strategies. J Mol Cell Cardiol 102:1-2
Unudurthi, Sathya D; Wu, Xiangqiong; Qian, Lan et al. (2016) Two-Pore K+ Channel TREK-1 Regulates Sinoatrial Node Membrane Excitability. J Am Heart Assoc 5:e002865