The endoplasmic reticulum chaperone improves insulin resistance in type 2 diabetes

被引:170
作者
Ozawa, K
Miyazaki, M
Matsuhisa, M
Takano, K
Nakatani, Y
Hatazaki, M
Tamatani, T
Yamagata, K
Miyagawa, JI
Kitao, Y
Hori, O
Yamasaki, Y
Ogawa, S
机构
[1] Kanazawa Univ, Sch Med, Dept Neuroanat, Kanazawa, Ishikawa 9208640, Japan
[2] Dainippon Pharmaceut Co, Dept Discovery Pharmacol 2, Pharmacol & Microbiol Res Labs, Drug Res Dis, Suita, Osaka, Japan
[3] Osaka Univ, Grad Sch Med, Dept Internal Med & Therapeut, Suita, Osaka, Japan
[4] Kanazawa Univ, Grad Sch Nat Sci & Technol, Mol Pharmacol Lab, Kanazawa, Ishikawa, Japan
[5] Osaka Univ, Grad Sch Med, Dept Internal Med & Mol Sci, Suita, Osaka, Japan
关键词
D O I
10.2337/diabetes.54.3.657
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To determine the role of the endoplasmic reticulum (ER) in diabetes, Akita mice, a mouse model of type 2 diabetes, were mated with either heterozygous knockout mice or two types of transgenic mice of 150-kDa oxygen-regulated protein (ORP150), a molecular chaperone located in the ER. Systemic expression of ORP150 in Akita mice improves insulin intolerance, whereas the exclusive overexpression of ORP150 in pancreatic beta-cells of Akita mice did not change their glucose tolerance. Both an insulin tolerance test and hyperinsulinemiceuglycemic clamp revealed that ORP150 enhanced glucose uptake, accompanied by suppression of oxidized protein. Furthermore, ORP150 enhanced the insulin sensitivity of myoblast cells treated with hydrogen peroxide. These data suggest that ORP150 plays an important role in insulin sensitivity and is a potential target for the treatment of diabetes.
引用
收藏
页码:657 / 663
页数:7
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