The skeletal muscle L-type Ca2+ channel (CaV1.1) in the transverse tubules, the ryanodine receptor (RyR1) in the sarcoplasmic reticulum (SR), and calsequestrin (Casq1) in the lumen of junctional SR (jSR) are key components of a macromolecular complex termed the couplon which regulates excitation-contraction coupling (ECC). Mutations in RyR1, CaV1.1, and Casq1 underlie human myopathies with overlapping pathological features. With the exception of dantrolene for malignant hyperthermia, there are no FDA approved interventions for any of these myopathies. Mice with a mutations CaV1.1 (E1014K), RyR1 (I4895T) and Casq1 (D244G) develop myopathies that increase in severity with age and their muscles display Casq1 mislocalization and persistent ER stress. This application is designed to elucidate the mechanisms by which mutation-associated alterations in a CaMKII-dependent pathway lead to ER stress/UPR and muscle disease. We will test the general hypothesis that the similarities in couplon myopathies arising from mutations in different couplon proteins are due to highly cooperative, bidirectional functional coupling between CaV1.1, CaMKII, RyR1 and Casq1.
Our aims are to: 1. Define the roles of altered CaV1.1 functional state transitions and CaMKII activation in couplon myopathies. 2. Quantify the effects of couplon disease-associated mutations on RyR1 phosphorylation and the phosphorylation-mediated effects on CaV1.1 function and Casq1 retention at the jSR. 3. Define the roles of Casq1 mislocalization and ER stress in the couplon myopathies. We will also test the ability of 4PBA, which alleviates ER stress, to improve muscle function in myopathies that arise from mutations in couplon proteins.

Public Health Relevance

This application is designed to elucidate the mechanism of the decline in muscle function associated with mutations in proteins in the couplon that underlie human myopathies. Specifically we will determine how the couplon mutations drive ER stress and an unfolded protein response and determine if a chemical chaperone can reverse the symptoms of the disease. We are attempting to identify interventions that are effective for myopathies arising from any one of the couplon proteins (CaV1.1, RyR1 or calsequestrin).

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Research Project (R01)
Project #
5R01AR072602-03
Application #
9970200
Study Section
Skeletal Muscle and Exercise Physiology Study Section (SMEP)
Program Officer
Boyce, Amanda T
Project Start
2018-08-01
Project End
2023-06-30
Budget Start
2020-07-01
Budget End
2021-06-30
Support Year
3
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Baylor College of Medicine
Department
Physiology
Type
Schools of Medicine
DUNS #
051113330
City
Houston
State
TX
Country
United States
Zip Code
77030