Le Lièvre C S
J Embryol Exp Morphol. 1978 Oct;47:17-37.
The differentiation of cephalic neural crest cells into skeletal tissue in birds has been observed using the quail-chick nuclear marking system, which is based on specific differences in the distribution of the nuclear DNA. Chimaeras were formed by replacing a fragment of cephalic neural primordium of a 2- to 12-somite chicken embryo by the corresponding fragment isolated from an equivalent quail embryo. The participation of the graft-derived cells in the formation of the skull of these embryos was studied on histological sections after Feulgen and Rossenbeck staining. Cells from the prosencephalic neural crest migrate into the frontal nasal process and mix with the mesencephalic neural crest cells in the lateral nasal processes, around the optic cupule and beneath the diencephalon. In addition, the mesencephalic neural crest cells form the bulk of the mesenchyme of the maxillary processes and mandibular arch, whereas the rhombencephalic neural crest cells become located in the branchial arches. The origin of cartilages of the chondrocranium and bones of the neurocranium and viscerocranium has been shown in the chimaeric embryos: the basal plate cartilages, occipital bones, sphenoid bones and the cranial vault are mainly of mesodermal origin. However some parts have a dual origin: rhombo-mesencephalic neural crest cells are found in the otic capsule, and the frontal bone, the rostrum of parasphenoid and the orbital cartilages contain diverse amounts of prosencephalo-mesencephalic neural crest cells. The squamosals and the columella auris are formed from mesectodermic cells as are the nasal skeleton, the palatines and the maxillar bones. The mesectodermal origin of mandibular and hyoid bones and cartilages was already known. From these results it appears that the cephalic neural crest is particularly important in the formation of the facial part of the skull, while the vault and dorsal part are mesodermal and cartilages and bones found in the intermediary region are of mixed origin. The presence of mixed structures implies that the mesoderm and the mesectoderm are equally competent towards the specific inducers of these bones and cartilages. This correlates with the equivalence in differentiation capacities already shown for cephalic mesodermal and mesectodermal mesenchymes.
利用鹌鹑 - 鸡细胞核标记系统,已观察到鸟类头部神经嵴细胞向骨骼组织的分化,该系统基于核DNA分布的特定差异。通过用从等效鹌鹑胚胎分离的相应片段替换2至12体节鸡胚胎头部神经原基的片段来形成嵌合体。在福尔根和罗森贝克染色后的组织切片上研究了移植来源的细胞在这些胚胎颅骨形成中的参与情况。前脑神经嵴的细胞迁移到额鼻突,并在外侧鼻突、视杯周围和间脑下方与中脑神经嵴细胞混合。此外,中脑神经嵴细胞构成上颌突和下颌弓间充质的大部分,而菱脑神经嵴细胞位于鳃弓中。在嵌合胚胎中已显示出软骨颅的软骨以及脑颅和脏颅的骨骼的起源:基板软骨、枕骨、蝶骨和颅顶主要起源于中胚层。然而,有些部分有双重起源:耳囊中发现菱 - 中脑神经嵴细胞,额骨、蝶骨体的喙和眶软骨含有不同数量的前脑 - 中脑神经嵴细胞。鳞骨和耳柱骨由中ectodermic细胞形成,鼻骨架、腭骨和上颌骨也是如此。下颌骨和舌骨及其软骨的中ectodermic起源早已为人所知。从这些结果看来,头部神经嵴在颅骨面部部分的形成中特别重要,而颅顶和背部是中胚层起源,中间区域发现的软骨和骨骼则是混合起源。混合结构的存在意味着中胚层和中ectoderm对这些骨骼和软骨的特定诱导物具有同等的能力。这与头部中胚层和中ectoderm间充质已显示出的分化能力的等效性相关。