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建立小鼠心室传导系统。

Establishment of the mouse ventricular conduction system.

机构信息

Developmental Biology Institute of Marseilles - Luminy, CNRS UMR6216 Université de la Méditerranée, Campus de Luminy, case 907, 13288 Marseille Cedex 9, France.

出版信息

Cardiovasc Res. 2011 Jul 15;91(2):232-42. doi: 10.1093/cvr/cvr069. Epub 2011 Mar 8.

Abstract

The ventricular conduction system represents the electrical wiring responsible for the co-ordination of cardiac contraction. Defects in the circuit produce a delay or conduction block and induce cardiac arrhythmias. Understanding how this circuit forms and identification of the factors important for its development thus provide insights into the origin of cardiac arrhythmias. Recent advances, using genetically modified mouse models, have contributed to our understanding of how the ventricular conduction system is established during heart development. Transgenic mice carrying different reporter genes have highlighted the conservation of the anatomy and development of the ventricular conduction system between mice and humans. Lineage tracing and retrospective clonal analysis have established the myogenic origin of the ventricular conduction system and determined properties of conductive progenitor cells. Finally, gene knock-out models reproducing human cardiac defects have led to the identification of transcription factors important for the development of the ventricular conduction system. These transcription factors operate at the levels of both conduction system morphogenesis and differentiation by controlling the expression of genes responsible for the electrical activity of the heart. In summary, defects in the ventricular conduction system are a major cause of arrhythmias, and deciphering the molecular pathways responsible for conduction system morphogenesis and the differentiation of conductive myocytes furthers our understanding of the mechanisms underlying heart disease.

摘要

心室传导系统代表了负责心脏收缩协调的电气布线。电路缺陷会导致延迟或传导阻滞,并引起心律失常。了解该电路如何形成以及确定对其发育重要的因素,从而深入了解心律失常的起源。最近,使用基因修饰的小鼠模型的进展有助于我们了解心室传导系统在心脏发育过程中是如何建立的。携带不同报告基因的转基因小鼠突出了小鼠和人类之间心室传导系统解剖结构和发育的保守性。谱系追踪和回溯性克隆分析确立了心室传导系统的肌源性起源,并确定了传导前体细胞的特性。最后,复制人类心脏缺陷的基因敲除模型导致了鉴定对心室传导系统发育重要的转录因子。这些转录因子通过控制负责心脏电活动的基因的表达,在传导系统形态发生和分化的水平上起作用。总之,心室传导系统缺陷是心律失常的主要原因,而阐明负责传导系统形态发生和传导性心肌细胞分化的分子途径,有助于我们深入了解心脏病的机制。

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