Unfolded protein response

• Published in: Current biology Vol. 22; no. 16; pp. R622 - R626
• Main Authors: Cao, Stewart Siyan, Kaufman, Randal J.
• Format: Journal Article
• Language: English
• Published: England Elsevier Inc 21.08.2012
• Subjects: Activating Transcription Factor 6 - metabolism; Animals; DNA-Binding Proteins - metabolism; eIF-2 Kinase - metabolism; Endoplasmic Reticulum Stress; Endoribonucleases - metabolism; Humans; Protein-Serine-Threonine Kinases - metabolism; Regulatory Factor X Transcription Factors; Transcription Factor CHOP - metabolism; Transcription Factors - metabolism; Unfolded Protein Response
• ISSN: 0960-9822; 1879-0445
• DOI: 10.1016/j.cub.2012.07.004

In eukaryotic cells, the endoplasmic reticulum (ER) is a membrane-enclosed interconnected organelle responsible for the synthesis, folding, modification, and quality control of numerous secretory and membrane proteins. The processes of protein folding and maturation are highly assisted and scrutinized but are also sensitive to changes in ER homeostasis, such as Ca2+ depletion, oxidative stress, hypoxia, energy deprivation, metabolic stimulation, altered glycosylation, activation of inflammation, as well as increases in protein synthesis or the expression of misfolded proteins or unassembled protein subunits. Only properly folded proteins can traffic to the Golgi apparatus, whereas those that misfold are directed to ER-associated degradation (ERAD) or to autophagy. The accumulation of unfolded/misfolded proteins in the ER activates signaling events to orchestrate adaptive cellular responses. This unfolded protein response (UPR) increases the ER protein-folding capacity, reduces global protein synthesis, and enhances ERAD of misfolded proteins.