MicroRNA-758 Regulates Cholesterol Efflux Through Posttranscriptional Repression of ATP-Binding Cassette Transporter A1

被引:238
作者
Ramirez, Cristina M.
Davalos, Alberto
Goedeke, Leigh
Salerno, Alessandro G.
Warrier, Nikhil
Cirera-Salinas, Daniel
Suarez, Yajaira
Fernandez-Hernando, Carlos
机构
[1] NYU, Sch Med, Dept Med, Leon H Charney Div Cardiol, New York, NY USA
[2] NYU, Sch Med, Dept Cell Biol, Leon H Charney Div Cardiol, New York, NY 10016 USA
[3] NYU, Sch Med, Marc & Ruti Bell Vasc Biol & Dis Program, New York, NY USA
基金
美国国家卫生研究院;
关键词
ABC transporter; atherosclerosis; lipids; lipoproteins; macrophages; HIGH-DENSITY-LIPOPROTEIN; LEUCINE ZIPPER PROTEIN; CENTRAL-NERVOUS-SYSTEM; RECEPTOR LXR-ALPHA; IN-VIVO; ALZHEIMER-DISEASE; TANGIER-DISEASE; MOUSE MODEL; ABCA1; HDL;
D O I
10.1161/ATVBAHA.111.232066
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective-The ATP-binding cassette transporter A1 (ABCA1) is a major regulator of macrophage cholesterol efflux and protects cells from excess intracellular cholesterol accumulation; however, the mechanism involved in posttranscriptional regulation of ABCA1 is poorly understood. We previously showed that microRNA-33 (miR-33) is 1 regulator. Here, we investigated the potential contribution of other microRNAs (miRNAs) to posttranscriptional regulation of ABCA1 and macrophage cholesterol efflux. Methods and Results-We performed a bioinformatic analysis for identifying miRNA target prediction sites in ABCA1 gene and an unbiased genome-wide screen to identify miRNAs modulated by cholesterol excess in mouse peritoneal macrophages. Quantitative real-time reverse transcription-polymerase chain reaction confirmed that miR-758 is repressed in cholesterol-loaded macrophages. Under physiological conditions, high dietary fat excess in mice repressed miR-758 both in peritoneal macrophages and, to a lesser extent, in the liver. In mouse and human cells in vitro, miR-758 repressed the expression of ABCA1, and conversely, the inhibition of this miRNA by using anti-miR-758 increased ABCA1 expression. In mouse cells, miR-758 reduced cellular cholesterol efflux to apolipoprotein A1 (apoA1), and anti-miR-758 increased it. miR-758 directly targets the 3'-untranslated region of Abca1 as assessed by 3'-untranslated region luciferase reporter assays. Interestingly, miR-758 is highly expressed in the brain, where it also targets several genes involved in neurological functions, including Slc38a1, Ntm, Epha7, and Mytl1. Conclusion-We identified miR-758 as a novel miRNA that posttranscriptionally controls ABCA1 levels in different cells and regulates macrophage cellular cholesterol efflux to apoA1, opening new avenues to increase apoA1 and raise high-density lipoprotein levels. (Arterioscler Thromb Vasc Biol. 2011;31:2707-2714.)
引用
收藏
页码:2707 / 2714
页数:8
相关论文
共 37 条
[1]   The functions of animal microRNAs [J].
Ambros, V .
NATURE, 2004, 431 (7006) :350-355
[2]   MicroRNAs: Target Recognition and Regulatory Functions [J].
Bartel, David P. .
CELL, 2009, 136 (02) :215-233
[3]   Genetic connections between neurological disorders and cholesterol metabolism [J].
Bjorkhem, Ingemar ;
Leoni, Valerio ;
Meaney, Steve .
JOURNAL OF LIPID RESEARCH, 2010, 51 (09) :2489-2503
[4]   Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency [J].
Brooks-Wilson, A ;
Marcil, M ;
Clee, SM ;
Zhang, LH ;
Roomp, K ;
van Dam, M ;
Yu, L ;
Brewer, C ;
Collins, JA ;
Molhuizen, HOF ;
Loubser, O ;
Ouelette, BFF ;
Fichter, K ;
Ashbourne-Excoffon, KJD ;
Sensen, CW ;
Scherer, S ;
Mott, S ;
Denis, M ;
Martindale, D ;
Frohlich, J ;
Morgan, K ;
Koop, B ;
Pimstone, S ;
Kastelein, JJP ;
Genest, J ;
Hayden, MR .
NATURE GENETICS, 1999, 22 (04) :336-345
[5]   A proteolytic pathway that controls the cholesterol content of membranes, cells, and blood [J].
Brown, MS ;
Goldstein, JL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (20) :11041-11048
[6]   Age and residual cholesterol efflux affect HDL cholesterol levels and coronary artery disease in ABCA1 heterozygotes [J].
Clee, SM ;
Kastelein, JJP ;
van Dam, M ;
Marcil, M ;
Roomp, K ;
Zwarts, KY ;
Collins, JA ;
Roelants, R ;
Tamasawa, N ;
Stulc, T ;
Suda, T ;
Ceska, R ;
Boucher, B ;
Rondeau, C ;
DeSouich, C ;
Brooks-Wilson, A ;
Molhuizen, HOF ;
Frohlich, J ;
Genest, J ;
Hayden, MR .
JOURNAL OF CLINICAL INVESTIGATION, 2000, 106 (10) :1263-1270
[7]   Cholesterol metabolism in the central nervous system during early development and in the mature animal [J].
Dietschy, JM ;
Turley, SD .
JOURNAL OF LIPID RESEARCH, 2004, 45 (08) :1375-1397
[8]   LNA-mediated microRNA silencing in non-human primates [J].
Elmen, Joacim ;
Lindow, Morten ;
Schutz, Sylvia ;
Lawrence, Matthew ;
Petri, Andreas ;
Obad, Susanna ;
Lindholm, Marie ;
Hedtjarn, Maj ;
Hansen, Henrik Frydenlund ;
Berger, Urs ;
Gullans, Steven ;
Kearney, Phil ;
Sarnow, Peter ;
Straarup, Ellen Marie ;
Kauppinen, Sakari .
NATURE, 2008, 452 (7189) :896-U10
[9]   miR-122 regulation of lipid metabolism revealed by in vivo antisense targeting [J].
Esau, C ;
Davis, S ;
Murray, SF ;
Yu, XX ;
Pandey, SK ;
Pear, M ;
Watts, L ;
Booten, SL ;
Graham, M ;
McKay, R ;
Subramaniam, A ;
Propp, S ;
Lollo, BA ;
Freier, S ;
Bennett, CF ;
Bhanot, S ;
Monia, BP .
CELL METABOLISM, 2006, 3 (02) :87-98
[10]   Deficiency of ABCA1 impairs apolipoprotein E metabolism in brain [J].
Hirsch-Reinshagen, V ;
Zhou, S ;
Burgess, BL ;
Bernier, L ;
McIsaac, SA ;
Chan, JY ;
Tansley, GH ;
Cohn, JS ;
Hayden, MR ;
Wellington, CL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (39) :41197-41207