Shen Xiaohua, Zhang Kezhong, Kaufman Randal J
Howard Hughes Medical Institute, The University of Michigan Medical Center, 1150 W. Medical Center Drive, Ann Arbor, MI 48109, USA.
J Chem Neuroanat. 2004 Sep;28(1-2):79-92. doi: 10.1016/j.jchemneu.2004.02.006.
The endoplasmic reticulum (ER) is a factory for folding and maturation of newly synthesized transmembrane and secretory proteins. The ER provides stringent quality control systems to ensure that only correctly folded proteins exit the ER and unfolded or misfolded proteins are retained and ultimately degraded. A number of biochemical and physiological stimuli can change ER homeostasis, impose stress to the ER, and subsequently lead to accumulation of unfolded or misfolded proteins in the ER lumen. The ER has evolved stress response signaling pathways collectively called the unfolded protein response (UPR) to cope with the accumulation of unfolded or misfolded proteins. This review summarizes our understanding of the UPR signaling developed in the recent years.
内质网(ER)是新合成的跨膜蛋白和分泌蛋白折叠与成熟的工厂。内质网提供严格的质量控制系统,以确保只有正确折叠的蛋白质才能离开内质网,而未折叠或错误折叠的蛋白质则被保留并最终降解。许多生化和生理刺激可改变内质网的稳态,给内质网施加压力,随后导致内质网腔中未折叠或错误折叠蛋白质的积累。内质网进化出了统称为未折叠蛋白反应(UPR)的应激反应信号通路,以应对未折叠或错误折叠蛋白质的积累。本综述总结了我们对近年来发展的UPR信号的理解。