Janssens Sophie, Pulendran Bali, Lambrecht Bart N
1] Unit Immunoregulation and Mucosal Immunology, VIB Inflammation Research Centre, Ghent, Belgium. [2] Ghent Researchers on Unfolded Proteins in Inflammation and Disease Consortium, Ghent University and University Hospital, Ghent, Belgium. [3] Department of Respiratory Medicine, Ghent University, Ghent, Belgium.
Emory Vaccine Center, Yerkes National Primate Center, Department of Pathology, Emory University, Atlanta, Georgia.
Nat Immunol. 2014 Oct;15(10):910-9. doi: 10.1038/ni.2991.
The unfolded protein response (UPR) has traditionally been viewed as an adaptive response triggered by the accumulation of unfolded proteins in the endoplasmic reticulum (ER) and aimed at restoring ER function. The UPR can also be an anticipatory response that is activated well before the disruption of protein homeostasis. UPR signaling intersects at many levels with the innate and adaptive immune responses. In some types of cells of the immune system, such as dendritic cells (DCs) and B cells, particular sensors that detect the UPR seem to be constitutively active in the absence of induction of the traditional UPR gene program and are necessary for antigen presentation and immunoglobulin synthesis. The UPR also influences signaling via Toll-like receptors (TLRs) and activation of the transcription factor NF-κB, and some pathogens subvert the UPR. This Review summarizes these emerging noncanonical functions of the UPR in immunity.
未折叠蛋白反应(UPR)传统上被视为一种适应性反应,由内质网(ER)中未折叠蛋白的积累触发,旨在恢复内质网功能。UPR也可以是一种预期反应,在蛋白质稳态破坏之前就被激活。UPR信号在多个层面与先天性和适应性免疫反应相互作用。在免疫系统的某些类型细胞中,如树突状细胞(DCs)和B细胞,检测UPR的特定传感器在未诱导传统UPR基因程序的情况下似乎组成性激活,并且对抗抗原呈递和免疫球蛋白合成是必需的。UPR还通过Toll样受体(TLRs)影响信号传导以及转录因子NF-κB的激活,并且一些病原体破坏UPR。本综述总结了UPR在免疫中的这些新出现的非经典功能。