Burns A J, Douarin N M
Institut d'Embryologie Cellulaire et Moléculaire, du CNRS et du Collège de France, Avenue de la Belle Gabrielle, France. Nicole.
Development. 1998 Nov;125(21):4335-47. doi: 10.1242/dev.125.21.4335.
The majority of the enteric nervous system is derived from vagal neural crest cells (NCC), which migrate to the developing gut, proliferate, form plexuses and differentiate into neurons and glia. However, for some time, controversy has existed as to whether cells from the sacral region of the neural crest also contribute to the enteric nervous system. The aim of this study was to investigate the spatiotemporal migration of vagal and sacral NCC within the developing gut and to determine whether the sacral neural crest contributes neurons and glia to the ENS. We utilised quail-chick chimeric grafting in conjunction with antibody labelling to identify graft-derived cells, neurons and glia. We found that vagal NCC migrated ventrally within the embryo and accumulated in the caudal branchial arches before entering the pharyngeal region and colonising the entire length of the gut in a proximodistal direction. During migration, vagal crest cells followed different pathways depending on the region of the gut being colonised. In the pre-umbilical intestine, NCC were evenly distributed throughout the splanchnopleural mesenchyme while, in the post-umbilical intestine, they occurred adjacent to the serosal epithelium. Behind this migration front, NCC became organised into the presumptive Auerbach's and Meissner's plexuses situated on either side of the developing circular muscle layer. The colorectum was found to be colonised in a complex manner. Vagal NCC initially migrated within the submucosa, internal to the circular muscle layer, before migrating outwards, adjacent to blood vessels, towards the myenteric plexus region. In contrast, sacral NCC, which also formed the entire nerve of Remak, were primarily located in the presumptive myenteric plexus region and subsequently migrated inwards towards the submucosal ganglia. Although present throughout the post-umbilical gut, sacral NCC were most numerous in the distal colorectum where they constituted up to 17% of enteric neurons, as identified by double antibody labelling using the quail-cell-specific marker, QCPN and the neuron-specific marker, ANNA-1. Sacral NCC were also immunopositive for the glial-specific antibody, GFAP, thus demonstrating that this region of the neural crest contributes neurons and glia to the enteric nervous system.
大多数肠神经系统起源于迷走神经嵴细胞(NCC),这些细胞迁移至发育中的肠道,增殖,形成神经丛,并分化为神经元和神经胶质细胞。然而,一段时间以来,关于神经嵴骶区的细胞是否也对肠神经系统有贡献一直存在争议。本研究的目的是调查迷走神经和骶神经NCC在发育中的肠道内的时空迁移情况,并确定骶神经嵴是否为肠神经系统贡献神经元和神经胶质细胞。我们利用鹌鹑 - 鸡嵌合移植结合抗体标记来识别移植来源的细胞、神经元和神经胶质细胞。我们发现,迷走神经NCC在胚胎内腹侧迁移,在进入咽部区域并沿近端到远端方向在整个肠道定植之前,先在尾鳃弓中积累。在迁移过程中,迷走神经嵴细胞根据所定植的肠道区域遵循不同的路径。在脐前肠,NCC均匀分布于整个脏壁中胚层,而在脐后肠,它们出现在浆膜上皮附近。在这个迁移前沿之后,NCC组织成位于发育中的环形肌层两侧的推定奥尔巴赫神经丛和迈斯纳神经丛。发现结肠直肠的定植方式较为复杂。迷走神经NCC最初在环形肌层内部的黏膜下层迁移,然后向外迁移,靠近血管,朝向肌间神经丛区域。相比之下,同样形成整个雷马克神经的骶神经NCC主要位于推定的肌间神经丛区域,随后向内迁移至黏膜下神经节。虽然在整个脐后肠都有骶神经NCC,但在远端结肠直肠中数量最多,通过使用鹌鹑细胞特异性标记物QCPN和神经元特异性标记物ANNA - 1的双抗体标记鉴定,它们在那里构成了高达17%的肠神经元。骶神经NCC对神经胶质特异性抗体GFAP也呈免疫阳性,因此表明神经嵴的这个区域为肠神经系统贡献了神经元和神经胶质细胞。