Abolishing Myofibroblast Arrhythmogeneicity by Pharmacological Ablation of alpha-Smooth Muscle Actin Containing Stress Fibers

作者：Rosker Christian; Salvarani Nicolo; Schmutz Stephan; Grand Teddy; Rohr Stephan^*

来源：Circulation Research, 2011, 109(10): 1120-1131.

DOI：10.1161/CIRCRESAHA.111.244798

• arrhythmia
• conduction
• fibroblast
• gap junction
• myocardial structure

Rationale: Myofibroblasts typically appear in the myocardium after insults to the heart like mechanical overload and infarction. Apart from contributing to fibrotic remodeling, myofibroblasts induce arrhythmogenic slow conduction and ectopic activity in cardiomyocytes after establishment of heterocellular electrotonic coupling in vitro. So far, it is not known whether alpha-smooth muscle actin (alpha-SMA) containing stress fibers, the cytoskeletal components that set myofibroblasts apart from resident fibroblasts, are essential for myofibroblasts to develop arrhythmogenic interactions with cardiomyocytes.
Objective: We investigated whether pharmacological ablation of alpha-SMA containing stress fibers by actin-targeting drugs affects arrhythmogenic myofibroblast-cardiomyocyte cross-talk.
Methods and Results: Experiments were performed with patterned growth cell cultures of neonatal rat ventricular cardiomyocytes coated with cardiac myofibroblasts. The preparations exhibited slow conduction and ectopic activity under control conditions. Exposure to actin-targeting drugs (Cytochalasin D, Latrunculin B, Jasplakinolide) for 24 hours led to disruption of alpha-SMA containing stress fibers. In parallel, conduction velocities increased dose-dependently to values indistinguishable from cardiomyocyte-only preparations and ectopic activity measured continuously over 24 hours was completely suppressed. Mechanistically, antiarrhythmic effects were due to myofibroblast hyperpolarization (Cytochalasin D, Latrunculin B) and disruption of heterocellular gap junctional coupling (Jasplakinolide), which caused normalization of membrane polarization of adjacent cardiomyocytes.
Conclusions: The results suggest that alpha-SMA containing stress fibers importantly contribute to myofibroblast arrhythmogeneicity. After ablation of this cytoskeletal component, cells lose their arrhythmic effects on cardiomyocytes, even if heterocellular electrotonic coupling is sustained. The findings identify alpha-SMA containing stress fibers as a potential future target of antiarrhythmic therapy in hearts undergoing structural remodeling. (Circ Res. 2011;109:1120-1131.)

• 出版日期2011-10-28