Transcriptional regulation of the GLUT4 gene:: from PPAR-γ and FOXO1 to FFA and inflammation

被引:98
作者
Armoni, Michal
Harel, Chava
Karnieli, Eddy [1 ]
机构
[1] Technion Israel Inst Technol, Rambam Med Ctr, Inst Endocrinol Diabet & Metab, IL-31096 Haifa, Israel
[2] Technion Israel Inst Technol, B Rappaport Fac Med, IL-31096 Haifa, Israel
基金
以色列科学基金会;
关键词
D O I
10.1016/j.tem.2007.02.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The insulin-responsive glucose transporter 4 (GLUT4) has a major role in glucose uptake and metabolism in insulin target tissues (i.e. adipose and muscle cells). In these tissues, the peroxisome proliferator-activated receptor (PPAR) family of nuclear receptors and the winged-helix-forkhead box class O (FOXO) family of factors are two key families of transcription factors that regulate glucose homeostasis and insulin responsiveness. Type 2 diabetes mellitus and obesity are associated with impaired regulation of GLUT4 gene expression and elevated levels of free fatty acids and proinflammatory factors. Based on our studies of the interplay between PPAR-gamma, FOXO1 and free fatty acids, and inflammation in regulating GLUT4 transcription in sickness and in health, we suggest a novel paradigm to increase insulin sensitivity in bona fide insulin target cells.
引用
收藏
页码:100 / 107
页数:8
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