IRE1 prevents endoplasmic reticulum membrane permeabilization and cell death under pathological conditions
Department of Molecular, Cell and Cancer Biology
Cell Biology | Cellular and Molecular Physiology
The endoplasmic reticulum (ER) has emerged as a critical regulator of cell survival. IRE1 is a transmembrane protein with kinase and RNase activities that is localized to the ER and that promotes resistance to ER stress. We showed a mechanism by which IRE1 conferred protection against ER stress-mediated cell death. IRE1 signaling prevented ER membrane permeabilization mediated by Bax and Bak and cell death in cells experiencing ER stress. Suppression of IRE1 signaling triggered by its kinase activity led to the accumulation of the BH3 domain-containing protein Bnip3, which in turn triggered the oligomerization of Bax and Bak in the ER membrane and ER membrane permeabilization. Consequently, in response to ER stress, cells deficient in IRE1 were susceptible to leakage of ER contents, which was associated with the accumulation of calcium in mitochondria, oxidative stress in the cytosol, and ultimately cell death. Our results reveal a role for IRE1 in preventing a cell death-initializing step that emanates from the ER and provide a potential target for treating diseases characterized by ER stress, including diabetes and Wolfram syndrome.
DOI of Published Version
Sci Signal. 2015 Jun 23;8(382):ra62. doi: 10.1126/scisignal.aaa0341. Link to article on publisher's site
Kanekura K, Ma X, Murphy JT, Zhu LJ, Diwan A, Urano F. (2015). IRE1 prevents endoplasmic reticulum membrane permeabilization and cell death under pathological conditions. Molecular, Cell and Cancer Biology Publications. https://doi.org/10.1126/scisignal.aaa0341. Retrieved from https://escholarship.umassmed.edu/mccb_pubs/40