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鸡胚体节发生的基于牵引的机制。

A traction-based mechanism for somitogenesis in the chick.

作者信息

Bard Jonathan B L

机构信息

MRC Clinical & Population Cytogenetics Unit, Western General Hospital, EH 4 2XU, Edinburgh, Scotland.

出版信息

Rouxs Arch Dev Biol. 1988 Jan;197(8):513-517. doi: 10.1007/BF00385686.

Abstract

This paper suggests that chick somites form because presomitic cells exert tractional forces on one another. These forces derive from the increase in cell adhesion and density that occurs as N-CAM and N-cadherin are laid down by the motile cells of the presomitic mesoderm, well before the somites form. Harris et al. (1984) have shown that adhesive and motile cells in an appropriate environment in vitro can spontaneously form aggregates under the influence of the tractional forces that they exert. Presomitic mesodermal cells may behave similarly: as CAM production increases local adhesivity, the tractional forces between the cells should become sufficiently strong for groups of cells to segment off the mesenchyme as somites. The successive expression of CAMs down the presomitic mesoderm will thus lead to the formation of an anterior-posterior sequence of somites. This mechanism can explain several aspects of somitogenesis that models generating a repetitive pre-pattern through gating cohorts of cells find hard to explain: first, mesodermal segregation occurs among highly adherent cells; second, that multiple rows of somites can form in embryos cultured on highly adherent substrata; third, that stirred mesoderm will still form normal somites; and, fourth, how somite size can be altered in heat-shocked embryos and elsewhere. Suggestions are given as to how the mechanism may be tested and where else in the embryo it could apply.

摘要

本文提出,鸡胚体节的形成是因为前体节细胞相互施加牵引力。这些力源于细胞黏附力和密度的增加,这是在体节形成之前,由前体节中胚层的运动细胞沉积N-CAM和N-钙黏蛋白时发生的。哈里斯等人(1984年)已经表明,在体外合适的环境中,具有黏附性和运动性的细胞在它们所施加的牵引力的影响下可以自发形成聚集体。前体节中胚层细胞可能表现得类似:随着细胞黏附分子的产生增加局部黏附性,细胞之间的牵引力应该会变得足够强大,使得细胞群从间充质中分割出来形成体节。因此,沿着前体节中胚层依次表达细胞黏附分子将导致形成前后序列的体节。这种机制可以解释体节发生的几个方面,而那些通过对细胞群体进行门控来产生重复预模式的模型很难解释这些方面:第一,中胚层分离发生在高度黏附的细胞之间;第二,在高度黏附的基质上培养的胚胎中可以形成多排体节;第三,搅拌的中胚层仍然会形成正常的体节;第四,热休克胚胎和其他地方的体节大小如何改变。文中还给出了关于如何测试该机制以及它在胚胎其他部位可能适用的建议。

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