Van Straaten H W, Janssen H C, Peeters M C, Copp A J, Hekking J W
Department of Anatomy/Embryology, University of Limburg, Maastricht, Netherlands.
Dev Dyn. 1996 Nov;207(3):309-18. doi: 10.1002/(SICI)1097-0177(199611)207:3<309::AID-AJA8>3.0.CO;2-L.
Progression of neurulation in the chick embryo has not been well documented. To provide a detailed description, chick embryos were stained in ovo after the least manipulation possible to avoid distortion of the neural plate and folds. This allowed a morphological and morphometric description of the process of neurulation in relatively undisturbed chick embryos. Neurulation comprises several specific phases with distinct closure patterns and closure rates. The first closure event occurs, de novo, in the future mesencephalon at the 4-6 somite stage (sst 4-6). Soon afterwards, at sst 6-7, de novo closure is seen at the rhombocervical level in the form of multisite contacts of the neural folds. These contacts occur in register with the somites, suggesting that the somites may play a role in forcing elevation and apposition of the neural folds. The mesencephalic] and rhombocervical closure events define an intervening rhombencephalic neuropore, which is present for a brief period before it closes. The remaining pear-shaped posterior neuropore (PNP) narrows and displaces caudally, but its length remains constant in embryos with seven to ten somites, indicating that the caudal extension of the rhombocervical closure point and elongation of the caudal neural plate are keeping pace with each other. From sst 10 onward, the tapered cranial portion of the PNP closes fast in a zipper-like manner, and, subsequently, the wide caudal portion of the PNP closes rapidly as a result of the parallel alignment of its folds, with numerous button-like temporary contact points. A role for convergent extension in this closure event is suggested. The final remnant of the PNP closes at sst 18. Thus, as in mammals, chick neurulation involves multisite closure and probably results form several different development mechanisms at varying levels of the body axis.
鸡胚神经胚形成的过程尚未得到充分记录。为了提供详细描述,在尽可能少的操作下对鸡胚进行卵内染色,以避免神经板和褶皱变形。这使得能够对相对未受干扰的鸡胚神经胚形成过程进行形态学和形态计量学描述。神经胚形成包括几个具有不同闭合模式和闭合速率的特定阶段。第一次闭合事件在4 - 6体节期(sst 4 - 6)于未来的中脑从头开始发生。此后不久,在sst 6 - 7时,在菱颈水平以神经褶的多位点接触形式出现从头闭合。这些接触与体节对齐,表明体节可能在促使神经褶抬高和并置方面发挥作用。中脑和菱颈闭合事件界定了一个中间的菱脑神经管孔,它在闭合前短暂存在。剩余的梨形后神经管孔(PNP)变窄并向尾侧移位,但其长度在有七到十个体节的胚胎中保持恒定,这表明菱颈闭合点向尾侧的延伸和尾侧神经板的伸长相互同步。从sst 10开始,PNP逐渐变细的颅部以拉链样方式快速闭合,随后,PNP宽阔的尾侧部分由于其褶皱的平行排列以及众多纽扣样临时接触点而迅速闭合。这表明趋同延伸在这一闭合事件中发挥作用。PNP的最终残余部分在sst 18时闭合。因此,与哺乳动物一样,鸡的神经胚形成涉及多位点闭合,并且可能是由身体轴不同水平的几种不同发育机制导致的。