Rutkowski D Thomas, Kaufman Randal J
Howard Hughes Medical Institute and Department of Biological Chemistry, University of Michigan Medical Center, Ann Arbor, MI 48109-0650, USA.
Trends Cell Biol. 2004 Jan;14(1):20-8. doi: 10.1016/j.tcb.2003.11.001.
The accumulation of unfolded proteins in the lumen of the endoplasmic reticulum (ER) induces a coordinated adaptive program called the unfolded protein response (UPR). The UPR alleviates stress by upregulating protein folding and degradation pathways in the ER and inhibiting protein synthesis. With a basic conceptual framework for the UPR, including the identification of key mediators of the response, now in place, recent work has turned towards investigating how the response is regulated and how its effects radiate beyond the immediate realm of protein secretion. This review highlights advances in these areas and attempts to forecast important issues that must be addressed soon.
内质网(ER)腔内未折叠蛋白的积累会引发一种名为未折叠蛋白反应(UPR)的协调适应性程序。UPR通过上调内质网中的蛋白质折叠和降解途径并抑制蛋白质合成来减轻应激。随着UPR基本概念框架的建立,包括对该反应关键介质的识别,目前的研究工作已转向探究该反应是如何被调控的,以及其影响如何扩散到蛋白质分泌的直接领域之外。本综述重点介绍了这些领域的进展,并试图预测一些亟待解决的重要问题。