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追溯桥粒的进化起源。

Tracing the Evolutionary Origin of Desmosomes.

机构信息

Departments of Pathology and Dermatology, Feinberg School of Medicine, Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, IL 60611, USA.

Departments of Pathology and Dermatology, Feinberg School of Medicine, Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, IL 60611, USA.

出版信息

Curr Biol. 2020 May 18;30(10):R535-R543. doi: 10.1016/j.cub.2020.03.047.

DOI:10.1016/j.cub.2020.03.047
PMID:32428495
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7310670/
Abstract

Cadherin-based cell-cell junctions help metazoans form polarized sheets of cells, which are necessary for the development of organs and the compartmentalization of functions. The components of the protein complexes that generate cadherin-based junctions have ancient origins, with conserved elements shared between animals as diverse as sponges and vertebrates. In invertebrates, the formation and function of epithelial sheets depends on classical cadherin-containing adherens junctions, which link actin to the plasma membrane through α-, β- and p120 catenins. Vertebrates also have a new type of cadherin-based intercellular junction called the desmosome, which allowed for the creation of more complex and effective tissue barriers against environmental stress. While desmosomes have a molecular blueprint that is similar to that of adherens junctions, desmosomal cadherins - called desmogleins and desmocollins - link intermediate filaments (IFs) rather than actin to the plasma membrane through protein complexes comprising relatives of β-catenin (plakoglobin) and p120 catenin (plakophilins). In turn, desmosomal catenins interact with members of the IF-binding plakin family to create the desmosome-IF linking complex. In this Minireview, we discuss when and how desmosomal components evolved, and how their ability to anchor the highly elastic and tough IF cytoskeleton endowed vertebrates with robust tissues capable of not only resisting but also properly responding to environmental stress.

摘要

基于钙黏蛋白的细胞-细胞连接有助于后生动物形成极化的细胞层,这对于器官的发育和功能的分隔是必要的。产生基于钙黏蛋白的连接的蛋白质复合物的组成部分具有古老的起源,在海绵和脊椎动物等多样化的动物之间共享保守元素。在无脊椎动物中,上皮层的形成和功能依赖于经典的含有钙黏蛋白的黏着连接,通过α-、β-和 p120 连环蛋白将肌动蛋白连接到质膜上。脊椎动物也有一种新的基于钙黏蛋白的细胞间连接,称为桥粒,这使得能够创建更复杂和有效的组织屏障来抵御环境压力。虽然桥粒具有与黏着连接相似的分子蓝图,但桥粒钙黏蛋白 - 称为桥粒芯糖蛋白和桥粒胶蛋白 - 通过包含β-连环蛋白(桥粒斑蛋白)和 p120 连环蛋白(桥粒斑蛋白)的亲属的蛋白复合物将中间丝 (IF) 而不是肌动蛋白连接到质膜上。反过来,桥粒连接蛋白与 IF 结合的 plakinin 家族成员相互作用,形成桥粒-IF 连接复合物。在这篇综述中,我们讨论了桥粒蛋白的组成部分是何时以及如何进化的,以及它们将高度弹性和坚韧的 IF 细胞骨架锚定的能力如何赋予脊椎动物具有强大的组织,不仅能够抵抗,而且能够正确应对环境压力。

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