Integrin beta 1D Deficiency-Mediated RyR2 Dysfunction Contributes to Catecholamine-Sensitive Ventricular Tachycardia in Arrhythmogenic Right Ventricular Cardiomyopathy

Article

关键词: CARDIAC RYANODINE RECEPTOR;    KINASE-A PHOSPHORYLATION;    HEART-FAILURE;    SUDDEN-DEATH;    ADRENERGIC RESPONSE;    HIGH PREVALENCE;    CALCIUM SPARKS;    1D INTEGRIN;    FOLLOW-UP;    PROTEIN;   

DOI  :  10.1161/CIRCULATIONAHA.119.043504

来源: SCIE

【 摘 要 】

Background: Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a hereditary heart disease characterized by fatty infiltration, life-threatening arrhythmias, and increased risk of sudden cardiac death. The guideline for management of ARVC in patients is to improve quality of life by reducing arrhythmic symptoms and to prevent sudden cardiac death. However, the mechanism underlying ARVC-associated cardiac arrhythmias remains poorly understood. Methods: Using protein mass spectrometry analyses, we identified that integrin beta 1 is downregulated in ARVC hearts without changes to Ca2+-handling proteins. As adult cardiomyocytes express only the beta 1D isoform, we generated a cardiac specific beta 1D knockout mouse model and performed functional imaging and biochemical analyses to determine the consequences of integrin beta 1D loss on function in the heart in vivo and in vitro. Results: Integrin beta 1D deficiency and RyR2 Ser-2030 hyperphosphorylation were detected by Western blotting in left ventricular tissues from patients with ARVC but not in patients with ischemic or hypertrophic cardiomyopathy. Using lipid bilayer patch clamp single channel recordings, we found that purified integrin beta 1D protein could stabilize RyR2 function by decreasing RyR2 open probability, mean open time, and increasing mean close time. Also, beta 1D knockout mice exhibited normal cardiac function and morphology but presented with catecholamine-sensitive polymorphic ventricular tachycardia, consistent with increased RyR2 Ser-2030 phosphorylation and aberrant Ca2+ handling in beta 1D knockout cardiomyocytes. Mechanistically, we revealed that loss of DSP (desmoplakin) induces integrin beta 1D deficiency in ARVC mediated through an ERK1/2 (extracellular signal-regulated kinase 1 and 2)-fibronectin-ubiquitin/lysosome pathway. Conclusions: Our data suggest that integrin beta 1D deficiency represents a novel mechanism underlying the increased risk of ventricular arrhythmias in patients with ARVC.

【 授权许可】

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