Effects of triglyceride on ER stress and insulin resistance

被引:45
|
作者
Kim, Do-Sung
Jeong, Seul-Ki
Kim, Hyung-Ryong
Kim, Dal-Sik
Chae, Soo-Wan
Chae, Han-Jung [1 ]
机构
[1] Chonbuk Natl Univ, Sch Med, Dept Pharmacol, Jeonju, Chonbuk, South Korea
[2] Chonbuk Natl Univ, Sch Med, Inst Cardiovasc Res, Jeonju, Chonbuk, South Korea
[3] Chonbuk Natl Univ, Sch Med, Dept Neurol, Jeonju, Chonbuk, South Korea
[4] Wonkwang Univ, Sch Dent, Dept Dent Pharmacol, Iksan, Chonbuk, South Korea
[5] Wonkwang Univ, Sch Dent, Wonkwang Biomat Implant Res Inst, Iksan, Chonbuk, South Korea
[6] Chonbuk Natl Univ, Sch Med, Dept Lab Med, Jeonju 560180, Chonbuk, South Korea
关键词
ER stress; triglyceride; insuline resistance; IRS-1; JNK;
D O I
10.1016/j.bbrc.2007.08.151
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This study was conducted to examine the mechanism by which triglyceride induces insulin resistance and ER stress in HepG2 cells. Using in vitro study models, we show that triglyceride causes insulin resistance through serine phosphorylation of insulin receptor substrate-1 (IRS-1). In addition, triglyceride induces the expression of endogenous endoplasmic reticulum, (ER) stress markers, including GRP 78, IRE-1alpha, XBP-1, p-eIF2alpha, CHOP, and p-JNK. ER stress, in turn, leads to the suppression of insulin receptor signaling through tyrosine dephosphorylation of IRS-1. The results of this study show that triglyceride is a central feature of peripheral insulin resistance, and also suggest that triglyceride-induced ER stress influences insulin resistance. These experiments may be used in the development of an in vitro acute obesity model. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:140 / 145
页数:6
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