[Cartilage differentiation in the limb bud of the chick embryo. Ultrastructural observations, culture and grafting experiments].

M Gumpel-Pinot
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Abstract

Differentiation of cartilage from mesodermal cells of the chick embryo wing bud is controlled by the ectoderm. Transfilter cultures have shown that this interaction cannot take place at a distance but requires contact conditions as established between mesodermal cells outgrowths and the ectodermal basement membrane in vivo and in vitro. Induction does not pass from one cell to another: when cultured in vitro cartilage differentiating cells do not provoke chondrogenic differentiation of mesodermal cells incapable of autonomous differentiation. During in vitro culture, cartilage differentiation of limb mesodermal cells is obtained in the absence of ectoderm at stage 17 (H. and H.) and rarely at stages 15-16. Is the inductive contact established at these stages for all the cells concerned or is it a continuous phenomenon which lasts as long as condensation formation proceeds? Ultrastructural studies of the space between ectoderm and mesoderm show that at stage 13 (18 to 20 somites), all limb somatopleural cells are capable of establishing a contact with the ectodermal basement membrane. But numerous contacts are also observed up to late stages, when condensations develop. However, at the stages and at the levels of formation of precartilaginous condensations, no movement of cells is observed from the external mesodermal layers towards the condensations, in chimeric quail-chick limbs. It seems therefore that the inductive contact takes place early (24-32 somites, stages 15 to 17 H. and H.), possibly a little later, but long before the formation of precartilaginous condensations (stages 23 to 30 H. and H.). The time between inductive contact and differentiation of the cell differs greatly therefore according to the final localization of the chondrocyte among the proximo-distal axis. This conclusions is discussed in relation to the Progress Zone (P.Z) concept.

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鸡胚肢芽的软骨分化。超微结构观察,培养和嫁接实验]。
鸡胚翼芽中胚层细胞向软骨的分化受外胚层控制。跨滤培养表明,这种相互作用不能在一定距离内发生,而需要在体内和体外中中胚层细胞生长和外胚层基底膜之间建立接触条件。诱导作用不会从一个细胞传递到另一个细胞:在体外培养时,软骨分化细胞不会引起不能自主分化的中胚层细胞的软骨分化。在体外培养过程中,肢中胚层细胞的软骨分化在17期(h和h)没有外胚层的情况下出现,在15-16期很少出现。感应接触是在这些阶段为所有相关的细胞建立的,还是它是一个持续的现象,只要冷凝形成进行?外胚层和中胚层间隙的超微结构研究表明,在第13期(18至20体体),所有肢体体胸膜细胞都能够与外胚层基膜建立接触。但是在冷凝发展的后期,也观察到许多接触。然而,在不稳定凝析物形成的阶段和水平上,没有观察到细胞从外部中胚层向凝析物移动,在鹌鹑-鸡嵌合肢体中。因此,感应接触似乎发生得较早(24-32点,阶段15至17 h和h),可能稍晚,但早于不稳定凝聚的形成(阶段23至30 h和h)。因此,根据软骨细胞在近端-远端轴之间的最终定位,诱导接触和细胞分化之间的时间差异很大。这些结论是与进步区(P.Z)概念有关的。
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