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桥粒芯蛋白家族的桥粒斑蛋白

The desmosomal plaque proteins of the plakophilin family.

作者信息

Neuber Steffen, Mühmer Mario, Wratten Denise, Koch Peter J, Moll Roland, Schmidt Ansgar

机构信息

Institute of Pathology, Philipps University of Marburg, Baldingerstrasse, 35033 Marburg, Germany.

出版信息

Dermatol Res Pract. 2010;2010:101452. doi: 10.1155/2010/101452. Epub 2010 Apr 21.

Abstract

Three related proteins of the plakophilin family (PKP1_3) have been identified as junctional proteins that are essential for the formation and stabilization of desmosomal cell contacts. Failure of PKP expression can have fatal effects on desmosomal adhesion, leading to abnormal tissue and organ development. Thus, loss of functional PKP 1 in humans leads to ectodermal dysplasia/skin fragility (EDSF) syndrome, a genodermatosis with severe blistering of the epidermis as well as abnormal keratinocytes differentiation. Mutations in the human PKP 2 gene have been linked to severe heart abnormalities that lead to arrhythmogenic right ventricular cardiomyopathy (ARVC). In the past few years it has been shown that junctional adhesion is not the only function of PKPs. These proteins have been implicated in cell signaling, organization of the cytoskeleton, and control of protein biosynthesis under specific cellular circumstances. Clearly, PKPs are more than just cell adhesion proteins. In this paper we will give an overview of our current knowledge on the very distinct roles of plakophilins in the cell.

摘要

桥粒芯蛋白家族的三种相关蛋白(PKP1_3)已被确定为连接蛋白,它们对于桥粒细胞连接的形成和稳定至关重要。PKP表达缺失会对桥粒黏附产生致命影响,导致组织和器官发育异常。因此,人类功能性PKP 1缺失会导致外胚层发育不良/皮肤脆性(EDSF)综合征,这是一种遗传性皮肤病,表现为表皮严重水疱形成以及角质形成细胞分化异常。人类PKP 2基因的突变与严重的心脏异常有关,可导致致心律失常性右室心肌病(ARVC)。在过去几年中,研究表明连接黏附并非PKP的唯一功能。这些蛋白还参与细胞信号传导、细胞骨架组织以及特定细胞环境下蛋白质生物合成的调控。显然,PKP不仅仅是细胞黏附蛋白。在本文中,我们将概述目前对桥粒芯蛋白在细胞中非常独特作用的认识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d52/2879962/dfae46c7559a/DRP2010-101452.001.jpg

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