The Unfolded Protein Response: From Stress Pathway to Homeostatic Regulation

被引:4590
作者
Walter, Peter [1 ,2 ]
Ron, David [3 ,4 ]
机构
[1] Univ Calif San Francisco, Howard Hughes Med Inst, San Francisco, CA 94158 USA
[2] Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94158 USA
[3] Univ Cambridge, Metab Res Lab, Cambridge CB2 0QQ, England
[4] Addenbrookes Hosp, NIHR Cambridge Biomed Res Ctr, Cambridge CB2 0QQ, England
基金
英国惠康基金;
关键词
ENDOPLASMIC-RETICULUM STRESS; TRANSCRIPTION FACTOR ATF6; ER-STRESS; MESSENGER-RNA; SENSOR IRE1; FACTOR XBP-1; B-CELLS; ACTIVATION; KINASE; REVEALS;
D O I
10.1126/science.1209038
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The vast majority of proteins that a cell secretes or displays on its surface first enter the endoplasmic reticulum (ER), where they fold and assemble. Only properly assembled proteins advance from the ER to the cell surface. To ascertain fidelity in protein folding, cells regulate the protein-folding capacity in the ER according to need. The ER responds to the burden of unfolded proteins in its lumen (ER stress) by activating intracellular signal transduction pathways, collectively termed the unfolded protein response (UPR). Together, at least three mechanistically distinct branches of the UPR regulate the expression of numerous genes that maintain homeostasis in the ER or induce apoptosis if ER stress remains unmitigated. Recent advances shed light on mechanistic complexities and on the role of the UPR in numerous diseases.
引用
收藏
页码:1081 / 1086
页数:6
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