Chronic over-nutrition and dysregulation of GSK3 in diseases

被引:24
|
作者
Liu, Xunxian [1 ]
Yao, Zemin [1 ]
机构
[1] Univ Ottawa, Ottawa Inst Syst Biol, Dept Biochem Microbiol & Immunol, 451 Smyth Rd, Ottawa, ON K1H 8M5, Canada
关键词
GLYCOGEN-SYNTHASE KINASE-3; DIFFERENTIATION-RELATED PROTEIN; PI3K/AKT SIGNALING PATHWAY; IMPROVES INSULIN SENSITIVITY; LIPID DROPLET FORMATION; INDUCED CELL-DEATH; P70; S6; KINASE; INDUCED APOPTOSIS; FATTY LIVER; PHOSPHATIDYLINOSITOL; 3-KINASE;
D O I
10.1186/s12986-016-0108-8
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Loss of cellular response to hormonal regulation in maintaining metabolic homeostasis is common in the process of aging. Chronic over-nutrition may render cells insensitive to such a hormonal regulation owing to overstimulation of certain signaling pathways, thus accelerating aging and causing diseases. The glycogen synthase kinase 3 (GSK3) plays a pivotal role in relaying various extracellular and intracellular regulatory signals critical to cell growth, survival, regeneration, or death. The main signaling pathway regulating GSK3 activity through serine-phosphorylation is the phosphoinositide 3-kinase (PI3K)/phosphoinositide-dependent kinase-1 (PDK1)/Akt relay that catalyzes serine-phosphorylation and thus inactivation of GSK3. In addition, perilipin 2 (PLIN2) has recently been shown to regulate GSK3 activation through direct association with GSK3. This review summarizes current understanding on environmental and nutritional factors contributing to GSK3 regulation (or dysregulation) through the PI3K/PDK1/Akt/GSK3 axis, and highlights the newly discovered role that PLIN2 plays in regulating GSK3 activity and GSK3 downstream pathways.
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页数:18
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