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Ⅰ型和Ⅱ型角蛋白中间丝。

Types I and II Keratin Intermediate Filaments.

机构信息

Department of Biochemistry and Molecular Biology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland 21205.

Departments of Biological Chemistry, Dermatology, and Oncology, School of Medicine, and Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, Maryland 21205.

出版信息

Cold Spring Harb Perspect Biol. 2018 Apr 2;10(4):a018275. doi: 10.1101/cshperspect.a018275.

Abstract

Keratins-types I and II-are the intermediate-filament-forming proteins expressed in epithelial cells. They are encoded by 54 evolutionarily conserved genes (28 type I, 26 type II) and regulated in a pairwise and tissue type-, differentiation-, and context-dependent manner. Here, we review how keratins serve multiple homeostatic and stress-triggered mechanical and nonmechanical functions, including maintenance of cellular integrity, regulation of cell growth and migration, and protection from apoptosis. These functions are tightly regulated by posttranslational modifications and keratin-associated proteins. Genetically determined alterations in keratin-coding sequences underlie highly penetrant and rare disorders whose pathophysiology reflects cell fragility or altered tissue homeostasis. Furthermore, keratin mutation or misregulation represents risk factors or genetic modifiers for several additional acute and chronic diseases.

摘要

角蛋白类型 I 和 II 是上皮细胞中表达的中间丝形成蛋白。它们由 54 个进化上保守的基因(28 种类型 I,26 种类型 II)编码,并以成对的、组织类型、分化和上下文依赖的方式进行调节。在这里,我们回顾了角蛋白如何发挥多种稳态和应激触发的机械和非机械功能,包括维持细胞完整性、调节细胞生长和迁移以及防止细胞凋亡。这些功能受到翻译后修饰和角蛋白相关蛋白的严格调控。角蛋白编码序列的遗传改变是高度外显和罕见疾病的基础,其病理生理学反映了细胞脆弱性或组织稳态的改变。此外,角蛋白突变或失调代表了几种额外的急性和慢性疾病的危险因素或遗传修饰因子。

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