AAV8-mediated delivery of FGF21 mitigated biventricular structural changes, decreased adrenergic arrhythmias, and rescued intracellular calcium imbalance in a PKP2-cKO mouse model of ACM.
Does AAV8-FGF21 gene therapy prevent catecholaminergic arrhythmias and rescue calcium regulation in a mouse model of PKP2 arrhythmogenic cardiomyopathy?
AAV8-FGF21 gene therapy mitigates structural changes, reduces adrenergic arrhythmias, and rescues intracellular calcium imbalance in a mouse model of PKP2 arrhythmogenic cardiomyopathy.
BACKGROUND Pathogenic variants in plakophilin-2 (PKP2) cause arrhythmogenic cardiomyopathy (ACM) with intracellular calcium dysregulation as a major component of its arrhythmia phenotype. Recent adeno-associated viral (AAV) based Pkp2 (AAV-PKP2) gene therapy has shown promising results in a few different PKP2-associated ACM models. Fibroblast growth factor 21 (FGF21) has multiple cardioprotective effects and has recently emerged as a promising therapeutic agent for cardiovascular disease. OBJECTIVES To assess the efficacy and impact on calcium regulation of a novel AAV8-based FGF21 gene therapy on adult cardiac-specific, tamoxifen-activated PKP2 knockout (PKP2-cKO) mice. METHODS Experiments were performed using a PKP2-cKO murine model. AAV8-FGF21 was delivered to adult mice by a single tail vein injection 7 days before tamoxifen-activated PKP2-cKO. Cardiac functions were monitored by echocardiography and electrocardiography. Intracellular calcium transients were investigated in acute isolated adult mouse cardiomyocytes and calcium fluorescent signals were acquired with the IonOptix system. RESULTS Loss of PKP2 expression caused cardiac mechanical dysfunction and pro-arrhythmic phenotype in adult mouse models. AAV-mediated delivery of FGF21 mitigated the progression of biventricular structural changes, decreased the occurrence of adrenergic arrhythmias, and rescued intracellular calcium imbalance in the setting of PKP2 haploinsufficiency. In contrast, acute in vitro FGF21 treatment for 1 hour had no effect on intracellular calcium transients. CONCLUSIONS These beneficial effects of AAV8-FGF21 on the PKP2-ACM phenotype suggest a therapeutic landscape for various targeted cardiomyopathies.
Lin et al. (Sun,) conducted a other in PKP2 arrhythmogenic cardiomyopathy. AAV8-FGF21 gene therapy was evaluated on Cardiac mechanical dysfunction, adrenergic arrhythmias, and intracellular calcium transients. AAV8-mediated delivery of FGF21 mitigated biventricular structural changes, decreased adrenergic arrhythmias, and rescued intracellular calcium imbalance in a PKP2-cKO mouse model of ACM.