Chen YiPing, Solursh Michael
Department of Biology, The University of Iowa, 52242, Iowa City, IA, USA.
Rouxs Arch Dev Biol. 1991 Aug;200(3):162-171. doi: 10.1007/BF00190236.
The time of determination of cartilage and skeletal muscle was studied by making chimeric grafts or explants of small tissue pieces from several stages of early chick or quail embryos. Chondrogenesis was assessed by histology or with antibodies directed against type II collagen or cartilage proteoglycan, while myogenesis was detected immunohistochemically with antibodies directed against 3 different muscle markers, including muscle myosin. Grafts from Hensen's node, primitive streak and segmental plate of donor embryos of Stage 3-5 (Hamburger and Hamilton) were transplanted under the ectoderm in the extraembryonic area of Stage 12 host embryos. In addition, explants and mesodermal cells were cultured on glass in DMEM+F12 medium supplemented with 10% FCS. The results showed that determined myogenic cells could first be detected in Hensen's node and the primitive streak at Stage 3-4 and that they developed from mesodermal cells located between the epiblast and hypoblast. Myogenic cells also appeared in grafted and explanted segmental plate with or without notochord from Stage 5 embryos. On the other hand, cartilage cells only formed in grafted and explanted segmental plate that also contained notochord. RA (1 ng/ml) could induce the formation of cartilage cells in the explanted primitive streak without Hensen's node or notochord taken from Stage 3-5 embryos and could also promote the differentiation of myogenic cells in primitive streak from Stage 3 embryo. Thus RA can substitute for Hensen's node or the notochord in the induction of cartilage cells and has some stimulatory effects on the differentiation of myogenic cells. Additional evidence indicates that the hypoblast might play an "inductive" role in the formation of the notochord which may subsequently promote the differentiation of cartilage cells.
通过制作来自早期鸡或鹌鹑胚胎几个阶段的小组织块的嵌合移植体或外植体,研究了软骨和骨骼肌的确定时间。通过组织学或使用针对II型胶原蛋白或软骨蛋白聚糖的抗体评估软骨形成,而通过使用针对3种不同肌肉标志物(包括肌肉肌球蛋白)的抗体进行免疫组织化学检测来检测肌发生。将第3 - 5阶段(汉堡和汉密尔顿)供体胚胎的亨氏结、原条和体节板的移植体移植到第12阶段宿主胚胎的胚外区域的外胚层下。此外,将外植体和中胚层细胞在补充有10%胎牛血清的DMEM + F12培养基中培养在玻璃上。结果表明,在第3 - 4阶段的亨氏结和原条中首先可以检测到确定的成肌细胞,并且它们由位于上胚层和下胚层之间的中胚层细胞发育而来。来自第5阶段胚胎的有或没有脊索的移植和外植体体节板中也出现了成肌细胞。另一方面,软骨细胞仅在也含有脊索的移植和外植体体节板中形成。视黄酸(1 ng/ml)可以诱导取自第3 - 5阶段胚胎的没有亨氏结或脊索的外植原条中软骨细胞的形成,并且还可以促进第3阶段胚胎原条中成肌细胞的分化。因此,视黄酸可以替代亨氏结或脊索来诱导软骨细胞的形成,并对成肌细胞的分化有一些刺激作用。额外的证据表明,下胚层可能在脊索的形成中起“诱导”作用,而脊索随后可能促进软骨细胞的分化。