High-methionine diets accelerate atherosclerosis by HHcy-mediated FABP4 gene demethylation pathway via DNMT1 in ApoE-/- mice

被引:54
|
作者
Yang, An-Ning [1 ]
Zhang, Hui-Ping [4 ]
Sun, Yue [1 ,4 ]
Yang, Xiao-Ling [1 ,4 ]
Wang, Nan [1 ]
Zhu, Guangrong [1 ]
Zhang, Hui [2 ]
Xu, Hua [1 ,4 ]
Ma, Sheng-Chao [2 ]
Zhang, Yue [3 ,4 ]
Li, Gui-Zhong [1 ,4 ]
Jia, Yue-Xia [1 ]
Cao, Jun [1 ]
Jiang, Yi-Deng [1 ,4 ]
机构
[1] Ningxia Med Univ, Sch Basic Med Sci, Dept Physiol & Pathophysiol, Yinchuan, Peoples R China
[2] Ningxia Med Univ, Dept Inspect Coll, Yinchuan, Peoples R China
[3] Ningxia Med Univ, Dept Foreign Language Teaching, Yinchuan, Peoples R China
[4] Ningxia Med Univ, Prenatal Diag Ctr, Gen Hosp, Yinchuan, Peoples R China
基金
中国国家自然科学基金;
关键词
Homocysteine; Atherosclerosis; Foam cell; Fatty acid-binding protein 4; DNA methylation; BINDING PROTEIN 4; DNA METHYLATION; PPAR-GAMMA; HYPERHOMOCYSTEINEMIA; EXPRESSION; DIFFERENTIATION; HOMOCYSTEINE; MACROPHAGES; DISEASE; ADIPOGENESIS;
D O I
10.1016/j.febslet.2015.11.010
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
Homocysteine (Hcy) is an independent risk factor for atherosclerosis, but the underlying molecular mechanisms are not known. We investigated the effects of Hcy on fatty acid-binding protein 4 (FABP4), and tested our hypothesis that Hcy-induced atherosclerosis is mediated by increased FABP4 expression and decreased methylation. The FABP4 expression and DNA methylation was assessed in the aorta of ApoE(-/-) mice fed high-methionine diet for 20 weeks. Over-expression of FABP4 enhanced accumulation of total cholesterol and cholesterol ester in foam cells. The upregulation of DNA methyltransferase 1 (DNMT1) promoted the methylation process and decreased FABP4 expression. These data suggest that FABP4 plays a key role in Hcy-mediated disturbance of lipid metabolism and that DNMT1 may be a novel therapeutic target in Hcy-related atherosclerosis. (C) 2015 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:3998 / 4009
页数:12
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