Männer J, Seidl W, Steding G
Abteilung Embryologie, Göttingen University, Germany.
Anat Embryol (Berl). 1993 Sep;188(3):269-85. doi: 10.1007/BF00188218.
The aim of the present study is to examine whether the formation of the cranial and cervical flexures is involved in the process of cardiac looping, and whether looping anomalies are causally involved in the development of cardiac malformations. For this purpose, the formation of the cranial and cervical flexures was experimentally suppressed in chick embryos by introducing a straight human hair into the neural tube. In the experimental embryos, the absence of the cervical flexure, alone or in combination with a reduced cranial flexure, was always associated with anomalies in the looping of the tubular heart. The convergence of the primary distant venous and arterial ends of the heart, as well as the normal movement of the ventricular region from its original position, cranial and ventral from the cardiac inflow, to its final position caudal to the presumptive atria, was suppressed to an extent related to the degree to which the formation of the flexures was prevented. Positional immaturity of the heart loop (increased distance between its inflow and outflow, and cranio-ventral position of the ventricular region) was associated with incomplete deformations (reduced angulations) of the cardiac wall at the atrioventricular or conoventricular junctional areas. Reduced angulations were associated with the hypoplasia of the anlagen of the cardiac septa at the level of the angulation (av-cushions, conal ridges). Hypoplasia of these anlagen was followed by incomplete or absent fusion of their opposite free edges, which finally resulted in atrioventricular or ventricular septal defects. These results show that the convergence of the venous and arterial ends of the tubular heart and the caudo-dorsal movement of its ventricular region are related to the formation of the cervical flexure, and that the mesenchymal septa of the heart seem to develop in response to deformations of the embryonic heart, which are generated by the process of cardiac looping. Therefore, the positional and morphological changes of the looping heart are regarded as playing a key role in the process of normal and abnormal morphogenesis of the heart.
本研究的目的是探讨颅曲和颈曲的形成是否参与心脏环化过程,以及环化异常是否与心脏畸形的发生有因果关系。为此,通过将一根直的人发插入神经管,在鸡胚中实验性地抑制颅曲和颈曲的形成。在实验胚胎中,颈曲缺失单独出现或与颅曲减小同时出现时,总是与管状心脏环化异常相关。心脏最初的远侧静脉端和动脉端的汇聚,以及心室区域从其原始位置(位于心脏流入端的颅侧和腹侧)向其最终位置(位于假定心房的尾侧)的正常移动,被抑制的程度与曲形成被阻止的程度相关。心脏环的位置不成熟(其流入端和流出端之间的距离增加,以及心室区域的颅腹位置)与房室或圆锥房室交界区域心脏壁的不完全变形(角度减小)相关。角度减小与角度水平处心脏间隔原基的发育不全相关(房室垫、圆锥嵴)。这些原基发育不全之后是其相对游离边缘的不完全融合或未融合,最终导致房室或室间隔缺损。这些结果表明,管状心脏的静脉端和动脉端的汇聚及其心室区域的尾背侧移动与颈曲的形成有关,并且心脏的间充质隔膜似乎是响应胚胎心脏的变形而发育的,这些变形是由心脏环化过程产生的。因此,环化心脏的位置和形态变化被认为在心脏正常和异常形态发生过程中起关键作用。