Duband J L, Dufour S, Hatta K, Takeichi M, Edelman G M, Thiery J P
J Cell Biol. 1987 May;104(5):1361-74. doi: 10.1083/jcb.104.5.1361.
In avian embryos, somites constitute the morphological unit of the metameric pattern. Somites are epithelia formed from a mesenchyme, the segmental plate, and are subsequently reorganized into dermatome, myotome, and sclerotome. In this study, we used somitogenesis as a basis to examine tissue remodeling during early vertebrate morphogenesis. Particular emphasis was put on the distribution and possible complementary roles of adhesion-promoting molecules, neural cell adhesion molecule (N-CAM), N-cadherin, fibronectin, and laminin. Both segmental plate and somitic cells exhibited in vitro calcium-dependent and calcium-independent systems of cell aggregation that could be inhibited respectively by anti-N-cadherin and anti-N-CAM antibodies. In vivo, the spatio-temporal expression of N-cadherin was closely associated with both the formation and local disruption of the somites. In contrast, changes in the prevalence of N-CAM did not strictly accompany the remodeling of the somitic epithelium into dermamyotome and sclerotome. It was also observed that fibronectin and laminin were reorganized secondarily in the extracellular spaces after CAM-mediated contacts were modulated. In an in vitro culture system of somites, N-cadherin was lost on individual cells released from somite explants and was reexpressed when these cells reached confluence and established intercellular contacts. In an assay of tissue dissociation in vitro, antibodies to N-cadherin or medium devoid of calcium strongly and reversibly dissociated explants of segmental plates and somites. Antibodies to N-CAM exhibited a smaller disrupting effect only on segmental plate explants. In contrast, antibodies to fibronectin and laminin did not perturb the cohesion of cells within the explants. These results emphasize the possible role of cell surface modulation of CAMs during the formation and remodeling of some transient embryonic epithelia. It is suggested that N-cadherin plays a major role in the control of tissue remodeling, a process in which N-CAM is also involved but to a lesser extent. The substratum adhesion molecules, fibronectin and laminin, do not appear to play a primary role in the regulation of these processes but may participate in cell positioning and in the stabilization of the epithelial structures.
在鸟类胚胎中,体节构成了分节模式的形态学单位。体节是由一种间充质即节段板形成的上皮组织,随后会重新组织形成生皮节、生肌节和生骨节。在本研究中,我们以体节发生为基础,研究早期脊椎动物形态发生过程中的组织重塑。特别强调了促进黏附分子、神经细胞黏附分子(N-CAM)、N-钙黏蛋白、纤连蛋白和层粘连蛋白的分布及可能的互补作用。节段板和体节细胞在体外均表现出钙依赖性和非钙依赖性细胞聚集系统,它们分别可被抗N-钙黏蛋白抗体和抗N-CAM抗体抑制。在体内,N-钙黏蛋白的时空表达与体节的形成和局部破坏密切相关。相比之下,N-CAM含量的变化并未严格伴随体节上皮向皮肌节和生骨节的重塑过程。还观察到,在CAM介导的接触被调节后,纤连蛋白和层粘连蛋白在细胞外空间中会继发重组。在体节的体外培养系统中,从体节外植体释放的单个细胞上N-钙黏蛋白会丢失,而当这些细胞达到汇合并建立细胞间接触时,N-钙黏蛋白会重新表达。在体外组织解离试验中,抗N-钙黏蛋白抗体或无钙培养基能强烈且可逆地使节段板和体节的外植体解离。抗N-CAM抗体仅对节段板外植体表现出较小的破坏作用。相比之下,抗纤连蛋白和抗层粘连蛋白抗体不会干扰外植体内细胞的黏附。这些结果强调了在一些短暂胚胎上皮的形成和重塑过程中,细胞表面CAM调节可能发挥的作用。研究表明,N-钙黏蛋白在组织重塑的控制中起主要作用,N-CAM也参与这一过程,但程度较小。细胞外基质黏附分子纤连蛋白和层粘连蛋白似乎在这些过程的调节中不发挥主要作用,但可能参与细胞定位和上皮结构的稳定。