Anderson Robert H, Spicer Diane E, Brown Nigel A, Mohun Timothy J
Institute of Genetic Medicine, Newcastle University, Newcastle, United Kingdom.
Anat Rec (Hoboken). 2014 Aug;297(8):1414-29. doi: 10.1002/ar.22949. Epub 2014 May 27.
The past decades have seen immense progress in the understanding of cardiac development. Appreciation of precise details of cardiac anatomy, however, has yet to be fully translated into the more general understanding of the changing structure of the developing heart, particularly with regard to formation of the septal structures. In this review, using images obtained with episcopic microscopy together with scanning electron microscopy, we show that the newly acquired information concerning the anatomic changes occurring during separation of the cardiac chambers in the mouse is able to provide a basis for understanding the morphogenesis of septal defects in the human heart. It is now established that as part of the changes seen when the heart tube changes from a short linear structure to the looped arrangement presaging formation of the ventricles, new material is added at both its venous and arterial poles. The details of these early changes, however, are beyond the scope of our current review. It is during E10.5 in the mouse that the first anatomic features of septation are seen, with formation of the primary atrial septum. This muscular structure grows toward the cushions formed within the atrioventricular canal, carrying on its leading edge a mesenchymal cap. Its cranial attachment breaks down to form the secondary foramen by the time the mesenchymal cap has used with the atrioventricular endocardial cushions, the latter fusion obliterating the primary foramen. Then the cap, along with a mesenchymal protrusion that grows from the mediastinal mesenchyme, muscularizes to form the base of the definitive atrial septum, the primary septum itself forming the floor of the oval foramen. The cranial margin of the foramen is a fold between the attachments of the pulmonary veins to the left atrium and the roof of the right atrium. The apical muscular ventricular septum develops concomitant with the ballooning of the apical components from the inlet and outlet of the ventricular loop. Its apical part is initially trabeculated. The membranous part of the septum is derived from the rightward margins of the atrioventricular cushions, with the muscularizing proximal outflow cushions fusing with the muscular septum and becoming the subpulmonary infundibulum as the aorta is committed to the left ventricle. Perturbations of these processes explain well the phenotypic variants of deficient atrial and ventricular septation.
在过去几十年里,我们对心脏发育的理解取得了巨大进展。然而,对心脏解剖结构精确细节的认识尚未完全转化为对发育中心脏结构变化的更全面理解,特别是在间隔结构形成方面。在本综述中,我们利用通过体表显微镜和扫描电子显微镜获得的图像表明,关于小鼠心脏腔室分离过程中发生的解剖学变化的新信息能够为理解人类心脏间隔缺损的形态发生提供基础。现在已经确定,作为心脏管从短的线性结构转变为预示心室形成的环状排列时所见到变化的一部分,新物质在其静脉极和动脉极都有添加。然而,这些早期变化的细节超出了我们当前综述的范围。在小鼠胚胎第10.5天(E10.5)时,首次出现间隔形成的解剖学特征,即初级房间隔的形成。这个肌肉结构朝着房室管内形成的心垫生长,其前缘带有一个间充质帽。当间充质帽与房室心内膜垫融合时,其头端附着处分解形成继发孔,后者的融合使原发孔消失。然后,该帽连同从中纵隔间充质长出的间充质突起一起肌化,形成最终房间隔的底部,初级隔本身形成卵圆孔的底部。卵圆孔的头端边缘是肺静脉与左心房连接处和右心房顶部之间的褶皱。心尖肌性室间隔随着心室环入口和出口处心尖部分的膨出而同时发育。其心尖部分最初是小梁状的。室间隔的膜部源自房室垫的右侧边缘,随着主动脉与左心室相连,肌化的近端流出道垫与肌性间隔融合并成为肺动脉下漏斗部。这些过程的紊乱很好地解释了房间隔和室间隔缺损的表型变异。