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N-钙黏蛋白/连环蛋白介导的体节形成的形态调节

N-cadherin/catenin-mediated morphoregulation of somite formation.

作者信息

Linask K K, Ludwig C, Han M D, Liu X, Radice G L, Knudsen K A

机构信息

Department of Cell Biology, University of Medicine and Dentistry of New Jersey, Stratford, NJ 08084, USA.

出版信息

Dev Biol. 1998 Oct 1;202(1):85-102. doi: 10.1006/dbio.1998.9025.

Abstract

Somitogenesis during early stages in the chick and mouse embryo was examined in relation to N-cadherin-mediated adhesion. Previous studies indicated that N-cadherin localizes to the somite regions during their formation. Those observations were extended to include a spatiotemporal immunohistochemical analyses of beta-catenin and alpha-catenin, as well as a more detailed study of N-cadherin, during segmentation, compaction, and compartmentalization of the somite. N-cadherin and the catenins appear early within the segmental plate and are expressed as small patch-like foci throughout this tissue. The small foci of immunostaining coalesce into larger clusters of N-cadherin/catenin-expressing regions. The clusters subsequently coalesce into a region of centrally localized cells that express N-cadherin/catenins at their apical surfaces. The multiple clusters are spaced wide apart in the anterior segmental plates that form the first 6 somite pairs, as contrasted to segmental plates that form somites 7 and beyond. To examine the functional significance of N-cadherin, segmental plates were exposed to antibodies that perturb N-cadherin-mediated adhesion in the chick embryo. The multiple, anomalous somites that result in these experiments indicate that each N-cadherin/catenin-expressing cluster can give rise to a somitic structure. beta-Catenin involvement in somitogenesis suggests a role for Wnt-mediated signaling. Embryos treated with LiCl also show induction of similar anomalous somites indicating further the possibility that Wnt-mediated signaling may be involved in the clustering event. It is suggested that beta-catenin serves to initiate the adhesion process which is spread then by N-cadherin. Later during compartmentalization, N-cadherin/catenins remain expressed by the myotome compartment. Taken together, these results suggest that the Ca2+-dependent cell adhesion molecule N-cadherin and the intracellular catenins are important in segmentation and formation of the somite and myotome compartment. It is proposed that the N-cadherin-mediated adhesion process may serve as a common, evolutionarily conserved, link in the differentiation pathways of skeletal and cardiac muscle.

摘要

研究了鸡和小鼠胚胎早期阶段的体节发生与N-钙黏蛋白介导的黏附之间的关系。先前的研究表明,N-钙黏蛋白在体节形成过程中定位于体节区域。这些观察结果被扩展到包括对β-连环蛋白和α-连环蛋白的时空免疫组织化学分析,以及在体节的分割、压实和分隔过程中对N-钙黏蛋白更详细的研究。N-钙黏蛋白和连环蛋白在节段板内早期出现,并在整个组织中表现为小的斑块状病灶。免疫染色的小病灶合并成表达N-钙黏蛋白/连环蛋白区域的更大簇。这些簇随后合并成中央定位细胞的区域,这些细胞在其顶端表面表达N-钙黏蛋白/连环蛋白。与形成第7及以后体节的节段板相比,在前6对体节的前节段板中,多个簇间隔很远。为了研究N-钙黏蛋白的功能意义,将节段板暴露于干扰鸡胚胎中N-钙黏蛋白介导黏附的抗体。这些实验中产生的多个异常体节表明,每个表达N-钙黏蛋白/连环蛋白的簇都可以产生一个体节结构。β-连环蛋白参与体节发生提示Wnt介导的信号传导起作用。用LiCl处理的胚胎也显示出类似异常体节的诱导,进一步表明Wnt介导的信号传导可能参与聚集事件的可能性。有人提出,β-连环蛋白用于启动黏附过程,然后由N-钙黏蛋白传播。在后期的分隔过程中,N-钙黏蛋白/连环蛋白仍由肌节隔室表达。综上所述,这些结果表明,Ca2+依赖性细胞黏附分子N-钙黏蛋白和细胞内连环蛋白在体节和肌节隔室的分割和形成中很重要。有人提出,N-钙黏蛋白介导的黏附过程可能是骨骼肌和心肌分化途径中一个共同的、进化上保守的环节。

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