Parvalbumin Corrects Slowed Relaxation in Adult Cardiac Myocytes Expressing Hypertrophic Cardiomyopathy-Linked α-Tropomyosin Mutations

Abstract

Hypertrophic cardiomyopathy mutations A63V and E180G in α-tropomyosin (α-Tm) have been shown to cause slow cardiac muscle relaxation. In this study, we used two complementary genetic strategies, gene transfer in isolated rat myocytes and transgenesis in mice, to ascertain whether parvalbumin (Parv), a myoplasmic calcium buffer, could correct the diastolic dysfunction caused by these mutations. Sarcomere shortening measurements in rat cardiac myocytes expressing the α-Tm A63V mutant revealed a slower time to 50% relengthening (T50R: 44.2±1.4 ms in A63V, 36.8±1.0 ms in controls; n=96 to 108; P+/PV⁻) had slower sarcomere relengthening kinetics than the controls (T90R: 199±7 ms in E180G⁺/PV⁻, 130±4 ms in E180G⁻/PV⁻; n=71 to 72), but when coexpressed with Parv, cellular relaxation was faster (T90R: 36±4 ms in E180G⁺/PV⁺). Collectively, these findings show that slow relaxation caused by α-Tm mutants can be corrected by modifying calcium handling with Parv.