诱导多能干细胞
骨形态发生蛋白4
Wnt信号通路
房室传导阻滞
心脏传导系统
干细胞
房室瓣
移植
细胞生物学
心脏病学
内科学
骨形态发生蛋白
医学
解剖
生物
胚胎干细胞
信号转导
心电图
生物化学
基因
心室
作者
ruohui Du,Shuyun Bai,Ya Li Zhao,Yue Ma
标识
DOI:10.1016/j.bbrc.2023.05.104
摘要
Atrioventricular conduction cardiomyocytes (AVCCs) regulate the rate and rhythm of heart contractions. Dysfunction due to aging or disease can cause atrioventricular (AV) block, interrupting electrical impulses from the atria to the ventricles. Generation of functional atrioventricular conduction like cardiomyocytes (AVCLCs) from human pluripotent stem cells (hPSCs) provides a promising approach to repair damaged atrioventricular conduction tissue by cell transplantation. In this study, we put forward the generation of AVCLCs from hPSCs by stage-specific manipulation of the retinoic acid (RA), WNT, and bone morphogenetic protein (BMP) signaling pathways. These cells express AVCC-specific markers, including the transcription factors TBX3, MSX2 and NKX2.5, display functional electrophysiological characteristics and present low conduction velocity (0.07 ± 0.02 m/s). Our findings provide new insights into the understanding of the development of the atrioventricular conduction system and propose a strategy for the treatment of severe atrioventricular conduction block by cell transplantation in future.
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