Peeters M C, Viebahn C, Hekking J W, van Straaten H W
Department of Anatomy/Embryology, University of Maastricht, The Netherlands.
Anat Embryol (Berl). 1998 Mar;197(3):167-75. doi: 10.1007/s004290050128.
Among a broad range of factors and mechanisms involved in the complex process of neurulation a relationship between the curvature of the craniocaudal body axis and rate of neural tube closure has been proposed, but more examples and models are needed to further substantiate the existence of this relationship. This is particularly true for mammals, where marked differences in embryonic body curvature between species exist. The rabbit embryo has virtually no curvature during the main phase of neurulation and is therefore a suitable model, but neurulation is hardly documented in this species. In the present study, therefore, neural tube closure in the rabbit embryo is presented in detail by morphological and morphometrical parameters, as well as from scanning electron microscopic investigations. At the stages of 6-8 somites, the flat neural plate transforms into a V-shaped neural groove, beginning at the rhombo-cervical level. Between the stages of 8 and 9 somites, multiple closure sites occur simultaneously at three levels: at the incipient pros-mesencephalic transition, at the incipient mes-rhombencephalic transition, and at the level of the first pairs of somites. This results in four transient neuropores. The anterior and rhombencephalic neuropores close between the stages of 9-11 somites. The mesencephalic neuropore is very briefly present. The posterior neuropore is the largest and remains longest. Its tapered (cranial) portion closes fast within somite stages 9-10. Subsequently its wide (caudal) portion closes up to a narrow slit, but further closure slows down till full closure is achieved at the 22-somite stage. In comparing rabbit neurulation with that of chick and mouse, the sequence of multiple site closure resembles that of the mouse embryo, but other important aspects of neurulation resemble those of the chick embryo. In contrast to mouse and chick, no time lag between closure at the three closure sites in the rabbit was seen.
在神经胚形成这一复杂过程涉及的众多因素和机制中,有人提出颅尾身体轴的曲率与神经管闭合速率之间存在关联,但需要更多实例和模型来进一步证实这种关系的存在。对于哺乳动物而言尤其如此,因为不同物种的胚胎身体曲率存在显著差异。兔胚胎在神经胚形成的主要阶段几乎没有曲率,因此是一个合适的模型,但该物种的神经胚形成过程几乎没有文献记载。因此,在本研究中,通过形态学和形态测量参数以及扫描电子显微镜研究,详细呈现了兔胚胎的神经管闭合过程。在6 - 8体节阶段,扁平的神经板从菱脑 - 颈段水平开始转变为V形神经沟。在8 - 9体节阶段之间,在三个水平同时出现多个闭合位点:在前脑 - 中脑起始过渡处、中脑 - 菱脑起始过渡处以及第一对体节水平。这导致形成四个暂时的神经孔。前神经孔和菱脑神经孔在9 - 11体节阶段之间闭合。中脑神经孔存在的时间非常短暂。后神经孔最大且持续时间最长。其逐渐变细的(头侧)部分在9 - 10体节阶段迅速闭合。随后其宽阔的(尾侧)部分闭合至一条窄缝,但进一步的闭合速度减缓,直至在22体节阶段完全闭合。将兔的神经胚形成过程与鸡和小鼠的进行比较,多个位点闭合的顺序与小鼠胚胎相似,但神经胚形成的其他重要方面与鸡胚胎相似。与小鼠和鸡不同,在兔的三个闭合位点之间未观察到时间延迟。