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多种钙黏着蛋白和连环蛋白在鸡视顶盖中的表达

Expression of multiple cadherins and catenins in the chick optic tectum.

作者信息

Miskevich F, Zhu Y, Ranscht B, Sanes J R

机构信息

Department of Anatomy and Neurobiology, Washington University School of Medicine, 660 S. Euclid Avenue, St. Louis, Missouri, 63110, USA.

出版信息

Mol Cell Neurosci. 1998 Nov;12(4-5):240-55. doi: 10.1006/mcne.1998.0718.

Abstract

Cadherins form a large family of homophilic cell adhesion molecules that are involved in numerous aspects of neural development. The best-studied neural cadherin, N-cadherin, is concentrated at synapses made by retinal axons in the chick optic tectum and is required for the arborization of retinal axons in their target (retinorecipient) laminae. By analogy, other cadherins might mediate arborization or synaptogenesis in other tectal laminae. Here we consider which cadherins are expressed in tectum, which cells express them, and how their expression is regulated. First, using N-cadherin as a model, we show that synaptic input regulates both cadherin gene expression and the subcellular distribution of cadherin protein. Second, we demonstrate that N-, R-, and T-cadherin are each expressed in distinct laminar patterns during retinotectal synaptogenesis and that N- and R- are enriched in nonoverlapping synaptic subsets. Third, we show that over 20 cadherin superfamily genes are expressed in the tectum during the time that synapses are forming and that many of them are expressed in restricted groups of cells. Finally, we report that both beta-catenin and gamma-catenin (plakoglobin), cytoplasmic proteins required for cadherin signaling, are enriched at synapses and associated with N-cadherin. However, beta- and gamma-catenins are differentially distributed and regulated, and form mutually exclusive complexes. This result suggests that cadherin-based specificity involves multiple cadherin-dependent signaling pathways as well as multiple cadherins.

摘要

钙黏着蛋白构成了一个庞大的同嗜性细胞黏附分子家族,参与神经发育的诸多方面。研究最为深入的神经钙黏着蛋白N-钙黏着蛋白,集中在鸡视顶盖中视网膜轴突形成的突触处,是视网膜轴突在其靶(视网膜接受)层进行分支所必需的。以此类推,其他钙黏着蛋白可能介导其他顶盖层中的分支或突触形成。在这里,我们探讨哪些钙黏着蛋白在顶盖中表达,哪些细胞表达它们,以及它们的表达是如何调控的。首先,以N-钙黏着蛋白为模型,我们表明突触输入调节钙黏着蛋白基因表达以及钙黏着蛋白的亚细胞分布。其次,我们证明在视网膜顶盖突触形成过程中,N-、R-和T-钙黏着蛋白各自以独特的分层模式表达,并且N-和R-在不重叠的突触亚群中富集。第三,我们表明在突触形成期间,超过20个钙黏着蛋白超家族基因在顶盖中表达,并且它们中的许多在特定的细胞群中表达。最后,我们报告β-连环蛋白和γ-连环蛋白(桥粒斑蛋白),这两种钙黏着蛋白信号传导所需的细胞质蛋白,在突触处富集并与N-钙黏着蛋白相关联。然而,β-连环蛋白和γ-连环蛋白的分布和调节存在差异,并形成相互排斥的复合物。这一结果表明基于钙黏着蛋白的特异性涉及多种钙黏着蛋白依赖性信号通路以及多种钙黏着蛋白。

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