Liu Yingying, Xu Chunling, Gu Renjun, Han Ruiqin, Li Ziyu, Xu Xianrong
Department of Aviation Clinical Medicine, Air Force Medical Center PLA Beijing China.
School of Pharmaceutical Sciences Tsinghua University Beijing China.
MedComm (2020). 2024 Aug 26;5(9):e701. doi: 10.1002/mco2.701. eCollection 2024 Sep.
The endoplasmic reticulum (ER) is a key organelle in eukaryotic cells, responsible for a wide range of vital functions, including the modification, folding, and trafficking of proteins, as well as the biosynthesis of lipids and the maintenance of intracellular calcium homeostasis. A variety of factors can disrupt the function of the ER, leading to the aggregation of unfolded and misfolded proteins within its confines and the induction of ER stress. A conserved cascade of signaling events known as the unfolded protein response (UPR) has evolved to relieve the burden within the ER and restore ER homeostasis. However, these processes can culminate in cell death while ER stress is sustained over an extended period and at elevated levels. This review summarizes the potential role of ER stress and the UPR in determining cell fate and function in various diseases, including cardiovascular diseases, neurodegenerative diseases, metabolic diseases, autoimmune diseases, fibrotic diseases, viral infections, and cancer. It also puts forward that the manipulation of this intricate signaling pathway may represent a novel target for drug discovery and innovative therapeutic strategies in the context of human diseases.
内质网(ER)是真核细胞中的关键细胞器,负责多种重要功能,包括蛋白质的修饰、折叠和运输,以及脂质的生物合成和细胞内钙稳态的维持。多种因素可破坏内质网的功能,导致未折叠和错误折叠的蛋白质在其内部聚集,并引发内质网应激。一种被称为未折叠蛋白反应(UPR)的保守信号事件级联反应已经进化出来,以减轻内质网内的负担并恢复内质网稳态。然而,当内质网应激在较长时间内持续且处于高水平时,这些过程可能最终导致细胞死亡。本综述总结了内质网应激和UPR在决定各种疾病(包括心血管疾病、神经退行性疾病、代谢疾病、自身免疫性疾病、纤维化疾病、病毒感染和癌症)中的细胞命运和功能方面的潜在作用。它还提出,在人类疾病的背景下,操纵这一复杂的信号通路可能代表药物发现和创新治疗策略的新靶点。