Knockout of the l-pgds gene aggravates obesity and atherosclerosis in mice

被引:49
作者
Tanaka, Reiko [1 ,2 ]
Miwa, Yoshikazu [1 ]
Mou, Kin [1 ]
Tomikawa, Morimasa [3 ]
Eguchi, Naomi [4 ]
Urade, Yoshihiro [4 ]
Takahashi-Yanaga, Fumi [1 ]
Morimoto, Sachio [1 ]
Wake, Norio [2 ]
Sasaguri, Toshiyuki [1 ]
机构
[1] Kyushu Univ, Fac Med Sci, Dept Clin Pharmacol, Higashi Ku, Fukuoka 8128582, Japan
[2] Kyushu Univ, Fac Med Sci, Dept Obstet & Gynecol, Fukuoka 8128582, Japan
[3] Kyushu Univ, Fac Med Sci, Dept Future Med & Innovat Med Informat, Fukuoka 8128582, Japan
[4] Osaka Biosci Inst, Dept Mol Behav Biol, Suita, Osaka 565, Japan
关键词
Lipocalin-type prostaglandin D synthase; Apolipoprotein E; Knockout mice; Atherosclerosis; Interleukin-1; beta; Monocyte chemoattractant protein type-1; Obesity; PROSTAGLANDIN-D-SYNTHASE; ACTIVATED RECEPTOR-GAMMA; 15-DEOXY-DELTA(12,14)-PROSTAGLANDIN J(2); D-2; EXPRESSION; METABOLITE; INCREASE;
D O I
10.1016/j.bbrc.2008.11.152
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 designed to determine whether lipocalin type-prostaglandin D synthase (l-pgds) deficiency contributes to atherogenesis using gene knockout (KO) mice. A high-fat diet was given to 8-week-old C57BL/6 (wild type; WT). l-pgds KO (LKO), apolipoprotein E (apo E) KO (AKO) and l-pgds/apo E double KO (DKO) mice. The l-pgds deficient mice showed significantly increased body weight, which was accompanied by increased size of subcutaneous and visceral fat tissues. Fat deposition in the aortic: wall induced by the high-fat diet was significantly increased in LKO mice compared with WT mice, although there was no significant difference between AKO and DKO mice. In LKO mice, atherosclerotic plaque in the aortic root was also increased and, furthermore, macrophage cellularity and the expression of pro-inflammatory cytokines such as interleukin-1 beta and monocyte chemoattractant protein-1 were significant increased. In conclusion, l-pgds deficiency induces obesity and facilitates atherosclerosis, probably through the regulation of inflammatory responses. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:851 / 856
页数:6
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