Colas J F, Schoenwolf G C
Department of Neurobiology and Anatomy, University of Utah School of Medicine, 50 N. Medical Drive, Salt Lake City, UT 84132, USA.
Dev Dyn. 2001 Jun;221(2):117-45. doi: 10.1002/dvdy.1144.
Neurulation occurs during the early embryogenesis of chordates, and it results in the formation of the neural tube, a dorsal hollow nerve cord that constitutes the rudiment of the entire adult central nervous system. The goal of studies on neurulation is to understand its tissue, cellular and molecular basis, as well as how neurulation is perturbed during the formation of neural tube defects. The tissue basis of neurulation consists of a series of coordinated morphogenetic movements within the primitive streak (e.g., regression of Hensen's node) and nascent primary germ layers formed during gastrulation. Signaling occurs between Hensen's node and the nascent ectoderm, initiating neurulation by inducing the neural plate (i.e., actually, by suppressing development of the epidermal ectoderm). Tissue movements subsequently result in shaping and bending of the neural plate and closure of the neural groove. The cellular basis of the tissue movements of neurulation consists of changes in the behavior of the constituent cells; namely, changes in cell number, position, shape, size and adhesion. Neurulation, like any morphogenetic event, occurs within the milieu of generic biophysical determinants of form present in all living tissues. Such forces govern and to some degree control morphogenesis in a tissue-autonomous manner. The molecular basis of neurulation remains largely unknown, but we suggest that neurulation genes have evolved to work in concert with such determinants, so that appropriate changes occur in the behaviors of the correct populations of cells at the correct time, maximizing the efficiency of neurulation and leading to heritable species- and axial-differences in this process. In this article, we review the tissue and cellular basis of neurulation and provide strategies to determine its molecular basis. We expect that such strategies will lead to the identification in the near future of critical neurulation genes, genes that when mutated perturb neurulation in a highly specific and predictable fashion and cause neurulation defects, thereby contributing to the formation of neural tube defects.
神经胚形成发生在脊索动物胚胎发育早期,其结果是形成神经管,即一条背侧中空的神经索,它构成了整个成年中枢神经系统的雏形。神经胚形成研究的目标是了解其组织、细胞和分子基础,以及在神经管缺陷形成过程中神经胚形成是如何受到干扰的。神经胚形成的组织基础包括原条内一系列协调的形态发生运动(例如亨氏结的退缩)以及原肠胚形成过程中形成的新生初级胚层。信号在亨氏结和新生外胚层之间传递,通过诱导神经板(实际上是通过抑制表皮外胚层的发育)启动神经胚形成。随后的组织运动导致神经板的塑形、弯曲以及神经沟的闭合。神经胚形成组织运动的细胞基础包括组成细胞行为的变化,即细胞数量、位置、形状、大小和黏附性的变化。与任何形态发生事件一样,神经胚形成发生在所有活组织中普遍存在的形态的一般生物物理决定因素的环境中。这些力量以组织自主的方式支配并在一定程度上控制形态发生。神经胚形成的分子基础在很大程度上仍然未知,但我们认为神经胚形成基因已经进化到与这些决定因素协同工作,以便在正确的时间在正确的细胞群体行为中发生适当的变化,最大限度地提高神经胚形成的效率,并导致这一过程中可遗传的物种和轴向差异。在本文中,我们回顾了神经胚形成的组织和细胞基础,并提供了确定其分子基础的策略。我们预计,这些策略将在不久的将来导致关键神经胚形成基因的鉴定,这些基因在发生突变时会以高度特异性和可预测的方式干扰神经胚形成并导致神经胚形成缺陷,从而导致神经管缺陷的形成。