Cardiovascular Research Institute.
Department of Molecular Physiology and Biophysics.
J Clin Invest. 2021 Oct 1;131(19). doi: 10.1172/JCI152185.
Loss of atrioventricular conduction system (AVCS) cells due to either inherited or acquired deficits leads to conduction diseases, which can deteriorate into fatal cardiac arrhythmias and sudden death. In this issue of the JCI, Wang et al. constructed a mouse model of atrioventricular block (AVB) by inducing AVCS cell-specific injury using the Cx30.2 enhancer to drive expression of diphtheria toxin fragment A. AVCS cell ablation in adult mice led to irreversible AVB. jkjkIn contrast, AVCS cell injury in neonatal mice was followed by spontaneous recovery in a subset of mice, revealing a limited postnatal time window during which the regeneration of AVCS cells can occur as a result of cellular plasticity. This exciting study paves the way for future research into biological or cellular treatment approaches for cardiac conduction diseases by exploiting the regenerative potential of AVCS cells.
由于遗传或获得性缺陷导致房室传导系统 (AVCS) 细胞丧失,会引发传导疾病,进而恶化为致命性心律失常和心源性猝死。在本期 JCI 中,Wang 等人构建了一种房室传导阻滞 (AVB) 的小鼠模型,通过使用 Cx30.2 增强子驱动白喉毒素片段 A 的表达,特异性损伤 AVCS 细胞。成年小鼠的 AVCS 细胞消融导致不可逆的 AVB。相比之下,新生小鼠的 AVCS 细胞损伤随后在一部分小鼠中自发恢复,这揭示了一个有限的出生后时间窗口,在此期间,由于细胞可塑性,AVCS 细胞可能发生再生。这项令人兴奋的研究为利用 AVCS 细胞的再生潜力,探索心脏传导疾病的生物或细胞治疗方法奠定了基础。