Reciprocal myocardial-endocardial interactions pattern the delay in atrioventricular junction conduction

被引:29
作者
Bressan, Michael [1 ]
Yang, PoAn Brian [1 ]
Louie, Jonathan D. [1 ]
Navetta, Alicia M. [1 ]
Garriock, Robert J. [1 ]
Mikawa, Takashi [1 ]
机构
[1] Univ Calif San Francisco, Cardiovasc Res Inst, San Francisco, CA 94143 USA
来源
DEVELOPMENT | 2014年 / 141卷 / 21期
基金
美国国家卫生研究院;
关键词
Action potential; Atrioventricular junction; Conduction velocity diversification; Heart patterning; Optical mapping; ENDOTHELIN-CONVERTING ENZYME-1; CARDIAC-VALVE FORMATION; CONGENITAL HEART-DEFECTS; EMBRYONIC HEART; TRANSCRIPTION FACTORS; SYSTEM-DEVELOPMENT; PURKINJE-FIBERS; HYALURONIC-ACID; IN-SITU; DIFFERENTIATION;
D O I
10.1242/dev.110007
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Efficient blood flow depends on two developmental processes that occur within the atrioventricular junction (AVJ) of the heart: conduction delay, which entrains sequential chamber contraction; and valve formation, which prevents retrograde fluid movement. Defects in either result in severe congenital heart disease; however, little is known about the interplay between these two crucial developmental processes. Here, we show that AVJ conduction delay is locally assigned by the morphogenetic events that initiate valve formation. Our data demonstrate that physical separation from endocardial-derived factors prevents AVJ myocardium from becoming fast conducting. Mechanistically, this physical separation is induced by myocardial-derived factors that support cardiac jelly deposition at the onset of valve formation. These data offer a novel paradigm for conduction patterning, whereby reciprocal myocardial-endocardial interactions coordinate the processes of valve formation with establishment of conduction delay. This, in turn, synchronizes the electrophysiological and structural events necessary for the optimization of blood flow through the developing heart.
引用
收藏
页码:4149 / 4157
页数:9
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