Adiponectin accelerates reverse cholesterol transport by increasing high density lipoprotein assembly in the liver

被引:128
作者
Matsuura, Fumihiko
Oku, Hiroyuki
Koseki, Masahiro
Sandoval, Jose C.
Yuasa-Kawase, Miyako
Tsubakio-Yamamoto, Kazumi
Masuda, Daisaku
Maeda, Norikazu
Tsujii, Ken-ichi
Ishigami, Masato
Nishida, Makoto
Hirano, Ken-ichi
Kihara, Shinji
Hori, Masatsugu
Shimomura, Iichiro
Yamashita, Shizuya
机构
[1] Osaka Univ, Dept Cardiovasc Med, Grad Sch Med, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Dept Metab Med, Grad Sch Med, Suita, Osaka 5650871, Japan
[3] Osaka Univ, Dept Biomed Informat, Grad Sch Med, Div Hlth Sci, Suita, Osaka 5650871, Japan
[4] Osaka Univ, Hlth Care Ctr, Toyonaka, Osaka 5600043, Japan
关键词
ABCA1; ABCG1; adiponectin; apolipoprotein A-1; apolipoprotein B; HDL; liver; metabolic syndrome; reverse cholesterol transport; SR-BI;
D O I
10.1016/j.bbrc.2007.05.040
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
Plasma high density lipoprotein (HDL)-cholesterol levels are negatively correlated with the incidence of coronary artery disease. HDL plays an important role in protecting against atherosclerosis by removing cholesterol from atheroma and transporting it back to the liver. The ATP-binding cassette transporters (ABCA1 and ABCG1) and scavenger receptor BI (SR-BI) are thought to be one of the rate-limiting factors to generate HDL in the liver. Adiponectin (APN) secreted from adipocytes is also one of the important molecules to inhibit the development of atherosclerosis. Recently, it has been reported that plasma HDL-cholesterol levels are positively correlated with plasma APN concentrations in humans. Therefore, we investigated the association of APN with HDL assembly in the liver. Human hepatoma cell line, HepG2 cells, were incubated for 24 h in the culture medium with the indicated concentrations of recombinant APN. APN enhanced the mRNA level of apolipoprotein A-I (apoA-I) in HepG2 cells and increased the secretion of apoA-I from the cells to the medium. Furthermore, APN increased both mRNA and protein levels of ABCA 1, but not ABCG1 and SR-BI, in HepG2 cells. Taken together, the current study demonstrates that APN might protect against atherosclerosis by increasing HDL assembly through enhancing ABCA1 pathway and apoA-I synthesis in the liver. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:1091 / 1095
页数:5
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