Gu Li-Hong, Coulombe Pierre A
Department of Biological Chemistry, Johns Hopkins University School of Medicine, 725 N. Wolfe St., Baltimore, MD 21205, USA.
Curr Opin Cell Biol. 2007 Feb;19(1):13-23. doi: 10.1016/j.ceb.2006.12.007. Epub 2006 Dec 18.
Keratins make up the largest subgroup of intermediate filament (IF) proteins and form a dynamic network of 10-12 nm filaments, built from type I/type II heterodimers, in the cytoplasm of epithelial cells. A major function of keratin IFs is to protect epithelial cells from mechanical and non-mechanical stresses that cause cell rupture and death. Interference with this role is the root cause of a large number of inherited epithelial fragility conditions. Additional functions, non-mechanical in nature, are manifested in a way that depends on the specific keratin and on the epithelial context. The recent discovery of unusual mutations affecting keratin proteins has uncovered a novel dimension of their mechanical support function, and has synergized with mouse genetics to reveal a role in skin pigmentation. Other studies extended the role of keratin proteins in regulating the response to pro-apoptotic signals, and revealed their ability to modulate protein synthesis and cell size in epithelial cells challenged to grow.
角蛋白构成中间丝(IF)蛋白的最大亚组,并在上皮细胞的细胞质中形成由I型/II型异二聚体构建的10 - 12纳米细丝的动态网络。角蛋白中间丝的主要功能是保护上皮细胞免受导致细胞破裂和死亡的机械和非机械应力。干扰这一作用是大量遗传性上皮脆弱病症的根本原因。其他非机械性质的功能以取决于特定角蛋白和上皮环境的方式表现出来。最近发现影响角蛋白的异常突变揭示了其机械支撑功能的新维度,并与小鼠遗传学协同作用,揭示了其在皮肤色素沉着中的作用。其他研究扩展了角蛋白在调节对促凋亡信号的反应中的作用,并揭示了它们在受挑战生长的上皮细胞中调节蛋白质合成和细胞大小的能力。