标题:Programmed cell death-4 deficiency prevents diet-induced obesity, adipose tissue inflammation, and insulin resistance
作者:Wang,Q.;Dong,Z.;Liu,X.;Song,X.;Song,Q.;Shang,Q.;Jiang,Y.;Guo,C.;Zhang,L.
作者机构:Department of Immunology, Shandong University School of Medicine, Jinan, Shangdong, China;Department of Immunology, Shandong Uni
通讯作者:Wang, Q
通讯作者地址:[Wang, Q]Shandong Univ, Sch Med, Dept Immunol, Jinan 250100, Shangdong, Peoples R China.
来源:Diabetes: A Journal of the American Diabetes Association
出版年:2013
卷:62
期:12
页码:4132-4143
DOI:10.2337/db13-0097
摘要:Programmed cell death-4 (PDCD4), a selective protein translation inhibitor, has shown proinflammatory effect in some inflammatory diseases, but its roles in obesity remain unestablished. This study aims to investigate the effects of PDCD4 on obesity, inflammation, and insulin resistance. Surprisingly, high-fat diet (HFD)-fed PDCD4-deficient (PDCD42/2) mice exhibited an absolutely lean phenotype together with improved insulin sensitivity. Compared with wild-type obese mice, HFD-fed PDCD42/2 mice showed higher energy expenditure, lower epididymal fat weight, and reduced macrophage infiltration inflammatory cytokine secretion in white adipose tissue (WAT). Alleviated hepatic steatosis along with decreased plasma levels of triglyceride and cholesterol was also observed in these mice. Importantly, PDCD4 appeared to disturb lipid metabolism via inhibiting the expression of liver X receptor (LXR)-a, a master modulator of lipid homeostasis, which was elevated in HFD-fed PDCD42/2 mice accompanied by upregulation of its target genes and relieved endoplasmic reticulum stress in WAT. These data demonstrate that PDCD4 deficiency protects mice against diet-induced obesity, WAT inflammation, and insulin resistance through restoring the expression of LXR-a, thereby proposing PDCD4 as a potential target for treating obesity-associated diseases.
收录类别:SCIE
WOS核心被引频次:15
资源类型:期刊论文
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