共 104 条
Regulation of basal cellular physiology by the homeostatic unfolded protein response
被引:310
作者:

Rutkowski, D. Thomas
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h-index: 0
机构:
Univ Iowa, Dept Anat & Cell Biol, Carver Coll Med, Iowa City, IA 52242 USA Univ Iowa, Dept Anat & Cell Biol, Carver Coll Med, Iowa City, IA 52242 USA

Hegde, Ramanujan S.
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h-index: 0
机构:
Eunice Kennedy Shriver Natl Inst Child Hlth & Hum, Cell Biol & Metab Program, NIH, Bethesda, MD 20892 USA Univ Iowa, Dept Anat & Cell Biol, Carver Coll Med, Iowa City, IA 52242 USA
机构:
[1] Univ Iowa, Dept Anat & Cell Biol, Carver Coll Med, Iowa City, IA 52242 USA
[2] Eunice Kennedy Shriver Natl Inst Child Hlth & Hum, Cell Biol & Metab Program, NIH, Bethesda, MD 20892 USA
基金:
美国国家卫生研究院;
关键词:
ENDOPLASMIC-RETICULUM STRESS;
TRANSCRIPTION FACTOR XBP1;
BOX-BINDING PROTEIN-1;
ER STRESS;
INSULIN-RESISTANCE;
TRANSLATIONAL CONTROL;
GLUCOSE-HOMEOSTASIS;
MESSENGER-RNA;
IN-VIVO;
B-CELLS;
D O I:
10.1083/jcb.201003138
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
The extensive membrane network of the endoplasmic reticulum (ER) is physically juxtaposed to and functionally entwined with essentially all other cellular compartments. Therefore, the ER must sense diverse and constantly changing physiological inputs so it can adjust its numerous functions to maintain cellular homeostasis. A growing body of new work suggests that the unfolded protein response (UPR), traditionally charged with signaling protein misfolding stress from the ER, has been co-opted for the maintenance of basal cellular homeostasis. Thus, the UPR can be activated, and its output modulated, by signals far outside the realm of protein misfolding. These findings are revealing that the UPR causally contributes to disease not just by its role in protein folding but also through its broad influence on cellular physiology.
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页码:783 / 794
页数:12
相关论文
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