Mucosal Diseases Program, Mater Medical Research Institute, Mater Health Services, South Brisbane, Qld 4029, Australia.
Am J Physiol Gastrointest Liver Physiol. 2010 Jun;298(6):G820-32. doi: 10.1152/ajpgi.00063.2010. Epub 2010 Mar 25.
Endoplasmic reticulum (ER) stress is a phenomenon that occurs when excessive protein misfolding occurs during biosynthesis. ER stress triggers a series of signaling and transcriptional events known as the unfolded protein response (UPR). The UPR attempts to restore homeostasis in the ER but if unsuccessful can trigger apoptosis in the stressed cells and local inflammation. Intestinal secretory cells are susceptible to ER stress because they produce large amounts of complex proteins for secretion, most of which are involved in mucosal defense. This review focuses on ER stress in intestinal secretory cells and describes how increased protein misfolding could occur in these cells, the process of degradation of misfolded proteins, the major molecular elements of the UPR pathway, and links between the UPR and inflammation. Evidence is reviewed from mouse models and human inflammatory bowel diseases that ties ER stress and activation of the UPR with intestinal inflammation, and possible therapeutic approaches to ameliorate ER stress are discussed.
内质网(ER)应激是一种在生物合成过程中蛋白质错误折叠过多时发生的现象。ER 应激会引发一系列被称为未折叠蛋白反应(UPR)的信号转导和转录事件。UPR 试图恢复 ER 中的内稳态,但如果不成功,可能会引发应激细胞凋亡和局部炎症。肠分泌细胞容易受到 ER 应激的影响,因为它们产生大量用于分泌的复杂蛋白质,其中大多数涉及黏膜防御。本文综述了肠分泌细胞中的 ER 应激,并描述了这些细胞中蛋白质错误折叠如何增加、错误折叠蛋白质的降解过程、UPR 途径的主要分子成分以及 UPR 与炎症之间的联系。本文从小鼠模型和人类炎症性肠病的证据中综述了 ER 应激和 UPR 的激活与肠道炎症之间的关系,并讨论了改善 ER 应激的可能治疗方法。