Coordinating Organismal Metabolism During Protein Misfolding in the ER Through the Unfolded Protein Response

被引:7
作者
Chandrahas, Vishwanatha K. [1 ]
Han, Jaeseok [2 ]
Kaufman, Randal J. [1 ]
机构
[1] Sanford Burnham Prebys Med Discovery Inst, Degenerat Dis Program, La Jolla, CA 92037 USA
[2] Soonchunhyang Univ, Soonchunhyang Inst Med Bio Sci SIMS, Cheonan Si 31151, Chungcheongnam, South Korea
来源
COORDINATING ORGANISMAL PHYSIOLOGY THROUGH THE UNFOLDED PROTEIN RESPONSE | 2018年 / 414卷
关键词
ENDOPLASMIC-RETICULUM STRESS; THIOREDOXIN-INTERACTING PROTEIN; PANCREATIC BETA-CELLS; SKELETAL-MUSCLE; FATTY-ACID; EXTRACELLULAR VESICLES; INSULIN-RESISTANCE; GENE-EXPRESSION; ADIPOSE-TISSUE; GLUCOSE-HOMEOSTASIS;
D O I
10.1007/82_2017_41
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The endoplasmic reticulum (ER) is a cellular organelle responsible for folding of secretory and membrane proteins. Perturbance in ER homeostasis caused by various intrinsic/extrinsic stimuli challenges the protein-folding capacity of the ER, leading to an ER dysfunction, called ER stress. Cells have developed a defensive response to adapt and/or survive in the face of ER stress that may be detrimental to cell function and survival. When exposed to ER stress, the cell activates a complex and elaborate signaling network that includes translational modulation and transcriptional induction of genes. In addition to these autonomous responses, recent studies suggest that the stressed tissue secretes peptides or unknown factors that transfer the signal to other cells in the same or different organs, leading the organism as a whole to cope with challenges in a non-autonomous manner. In this review, we discuss the mechanisms by which cells adapt to ER stress challenges autonomously and transfer the stress signal to non-stressed cells in different organs.
引用
收藏
页码:103 / 130
页数:28
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