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房室结:起源、发育和遗传程序。

The atrioventricular node: origin, development, and genetic program.

机构信息

Heart Failure Research Center, Academic Medical Center, Amsterdam, The Netherlands.

出版信息

Trends Cardiovasc Med. 2010 Jul;20(5):164-71. doi: 10.1016/j.tcm.2011.02.001.

Abstract

The sinus node generates the electrical impulse, which spreads rapidly over both atria, causing them to contract simultaneously. In the normal heart, a layer of connective tissue electrically insulates the atria and ventricles. The only pathway that crosses this plane is the atrioventricular conduction axis, through which the impulse reaches the ventricles. Within the axis, the atrioventricular node delays the impulse, allowing the ventricles to be filled before their contraction is initiated. Moreover, the atrioventricular node protects the ventricles from rapid atrial arrhythmias and may take over pacemaker function when the sinus node fails. In pathological conditions, these complex physiological properties contribute to several types of arrhythmias that originate from the atrioventricular conduction system. One example is atrioventricular block, which requires electronic pacemaker implantation because there is currently no cure for this arrhythmia. Because conduction system defects may arise during embryonic development, the mechanisms of conduction system development have been intensively studied. Nevertheless, its developmental origin, molecular composition, and phenotype have remained fertile subjects of research and debate. Lineage and expressional analyses have indicated that the atrioventricular node develops from a subpopulation of precursor cells in the dorsal part of the embryonic atrioventricular canal. These cells become distinct early in development, are less well differentiated compared to the developing working myocardium, and, in addition to their cardiogenic gene program, activate and maintain a neurogenic gene program.

摘要

窦房结产生电脉冲,迅速传遍左右心房,使它们同时收缩。在正常心脏中,一层结缔组织将心房和心室电隔离。唯一穿过这个平面的通路是房室传导轴,冲动通过这个通路到达心室。在轴内,房室结延迟冲动,使心室在收缩前充盈。此外,房室结保护心室免受快速性房性心律失常的影响,当窦房结功能衰竭时,房室结可能会接管起博器的功能。在病理条件下,这些复杂的生理特性导致了几种起源于房室传导系统的心律失常。例如房室传导阻滞,需要植入电子起搏器,因为目前这种心律失常还没有治愈方法。由于传导系统缺陷可能在胚胎发育过程中出现,因此人们已经对传导系统的发育机制进行了深入研究。然而,其发育起源、分子组成和表型仍然是研究和争论的热门话题。谱系和表达分析表明,房室结由胚胎房室管背侧的一小部分前体细胞发育而来。这些细胞在发育早期就变得明显,与发育中的工作心肌相比,分化程度较低,除了具有心脏生成基因程序外,还激活并维持神经生成基因程序。

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