| Literature DB >> 33685797 |
Eelco van Anken1, Anush Bakunts2, Chih-Chi Andrew Hu3, Sophie Janssens4, Roberto Sitia5.
Abstract
The biosynthesis of about one third of the human proteome, including membrane receptors and secreted proteins, occurs in the endoplasmic reticulum (ER). Conditions that perturb ER homeostasis activate the unfolded protein response (UPR). An 'optimistic' UPR output aims at restoring homeostasis by reinforcement of machineries that guarantee efficiency and fidelity of protein biogenesis in the ER. Yet, once the UPR 'deems' that ER homeostatic readjustment fails, it transitions to a 'pessimistic' output, which, depending on the cell type, will result in apoptosis. In this article, we discuss emerging concepts on how the UPR 'evaluates' ER stress, how the UPR is repurposed, in particular in B cells, and how UPR-driven counter-selection of cells undergoing homeostatic failure serves organismal homeostasis and humoral immunity.Entities:
Keywords: B cell development; RIDD; antibody production; endoplasmic reticulum; proteostasis; unfolded protein response
Mesh:
Year: 2021 PMID: 33685797 PMCID: PMC7611675 DOI: 10.1016/j.tcb.2021.02.004
Source DB: PubMed Journal: Trends Cell Biol ISSN: 0962-8924 Impact factor: 20.808