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摘要:
The signal transduction network in regulating lipid metabolism is a hot topic of biomedical research. Recent research endeavors reveal that intracellular stress signaling from a cellular organelle called endoplasmic reticulum (ER) is critically involved in lipid homeostasis and the development of metabolic disease. The ER is a site where newly-synthesized proteins are folded and assembled into their three-dimensional structures, modified and transported to their precise cellular destinations. A wide range of biochemical, physiological and pathological stimuli can interrupt the protein folding process in the ER and cause accumulation of unfolded or misfolded proteins in the ER lumen, a condition referred to as ER stress. To cope with this stress condition, the ER has evolved highly-specifi c signaling pathways collectively termed Unfolded Protein Response (UPR) or ER stress response. The UPR regulates transcriptionaland translational programs, affecting broad aspects of cellular metabolism and cell fate. Lipogenesis, the metabolic process of de novo lipid biosynthesis, occurs primarily in the liver where metabolic signals regulate expression of key enzymes in glycolytic and lipogenic pathways. Recent studies suggest that the UPR plays crucial roles in modulating lipogenesis under metabolic conditions. Here we address some of recent representative evidence regarding the role of the UPR in lipogenesis.
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篇名 在 lipogenesis 的展开的蛋白质反应的角色
来源期刊 世界肝病学杂志:英文版(电子版) 学科 医学
关键词 Endoplasmic reticulum stress Unfolded PROTEIN response LIPOGENESIS HEPATIC LIPID METABOLISM METABOLIC disease
年,卷(期) sjgbxzzywbdzb_2010,(6) 所属期刊栏目
研究方向 页码范围 203-207
页数 5页 分类号 R329
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Endoplasmic
reticulum
stress
Unfolded
PROTEIN
response
LIPOGENESIS
HEPATIC
LIPID
METABOLISM
METABOLIC
disease
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世界肝病学杂志:英文版(电子版)
月刊
1948-5182
北京市朝阳区东四环中路62号楼远洋国际中
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381
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