Inserm U1242, University of Rennes, Rennes, France.
Inserm U1242, University of Rennes, Rennes, France; Centre de Lutte Contre le Cancer Eugène Marquis, Rennes, France.
Biochim Biophys Acta Mol Cell Res. 2021 May;1868(6):119001. doi: 10.1016/j.bbamcr.2021.119001. Epub 2021 Mar 9.
Endoplasmic Reticulum (ER) stress signaling is an adaptive mechanism triggered when protein folding demand overcomes the folding capacity of this compartment, thereby leading to the accumulation of improperly folded proteins. This stress signaling pathway is named the Unfolded Protein Response (UPR) and aims at restoring ER homeostasis. However, if this fails, mechanisms orienting cells towards death processes are initiated. Herein, we summarize the most recent findings connecting ER stress and the UPR with identified death mechanisms including apoptosis, necrosis, pyroptosis, ferroptosis, and autophagy. We highlight new avenues that could be investigated and controlled through actionable mechanisms in physiology and pathology.
内质网(ER)应激信号是一种适应性机制,当蛋白质折叠需求超过这个隔室的折叠能力时触发,从而导致错误折叠的蛋白质积累。这条应激信号通路被命名为未折叠蛋白反应(UPR),旨在恢复内质网的平衡。然而,如果这失败了,就会启动引导细胞走向死亡过程的机制。在此,我们总结了将 ER 应激和 UPR 与已确定的死亡机制(包括细胞凋亡、细胞坏死、细胞焦亡、铁死亡和自噬)联系起来的最新发现。我们强调了新的途径,这些途径可以通过生理学和病理学中的可行机制进行研究和控制。