[Embryological and genetic mechanisms of cardiac great arteries malformations].

Journal de la Societe de biologie Pub Date : 2009-01-01 Epub Date: 2009-06-16 DOI:10.1051/jbio/2009019
Damien Bonnet, Stéphane Zaffran, Robert Kelly, Fanny Bajolle
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引用次数: 1

Abstract

Developmental genetics of congenital heart diseases have evolved from analysis of embryonic hearts towards molecular genetics of cardiac morphogenesis with a dynamic view of cardiac development. Ablation techniques, transgenic animal models and clonal analysis of the developing heart led to identification of different cardiac lineages and their respective roles. The mechanistic approach for great arteries anomalies has led to emerging concepts such as common embryological origin of anatomically different cardiac defects, phenotypic continuum of left heart obstructive defects, or developmental algorithms for cardiac isomerisms. Recent experiments that demonstrated the myocardial rotation of the outflow tract in mouse embryos led to a better understanding of the origin of transposition of the large arteries. This has also raised the hypothesis of a new group of congenital heart anomalies defined as laterality defects limited to a segment of the embryonic heart. These results confirm that genetic heterogeneity of congenital heart defects is related to the heterogeneity of the mechanisms that finally produce the same phenotype.

[心脏大动脉畸形的胚胎学和遗传机制]。
先天性心脏病的发育遗传学已经从胚胎心脏的分析发展到心脏形态发生的分子遗传学和心脏发育的动态观点。消融技术、转基因动物模型和发育中的心脏克隆分析鉴定了不同的心脏谱系及其各自的作用。大动脉异常的机制方法导致了一些新兴的概念,如解剖学上不同心脏缺陷的共同胚胎起源,左心阻塞性缺陷的表型连续体,或心脏异构体的发育算法。最近的实验证明了小鼠胚胎流出道的心肌旋转,从而更好地理解了大动脉转位的起源。这也提出了一种新的假设,即先天性心脏畸形被定义为局限于胚胎心脏的一部分的侧边缺陷。这些结果证实,先天性心脏缺陷的遗传异质性与最终产生相同表型的机制的异质性有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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