Statins downregulate myeloperoxidase gene expression in macrophages

被引:85
作者
Kumar, AP [1 ]
Reynolds, WF [1 ]
机构
[1] Sidney Kimmel Canc Ctr, San Diego, CA 92121 USA
关键词
myeloperoxidase; statins; simvastatin; oxidation inflammation; atherosclerosis; Alzheimer's disease; multiple sclerosis; macrophage; gene expression;
D O I
10.1016/j.bbrc.2005.03.204
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
Statins, inhibitors of HMG-CoA reductase. have pleiotropic benefits independent of cholesterol levels, including anti-oxidant and anti-inflammatory effects. Here, we investigate the effect of statins on myeloperoxidase (MPO) expression. MPO expressed in foam cell macrophages, was recently shown to oxidize the ApoA-1 component of HDL, impairing, ABCA-1 Mediated cholesterol efflux. High levels of serum MPO correlate with increased risk of CAD events. Findings here show that statins strongly inhibit MPO mRNA expression in human and murine monocyte-macrophages. Suppression was reversed by downstream intermediates of HMG-CoA reductase, mevalonate, and geranylgeranylpyrophosphate, but not farnesylpyrophosphate, An inhibitor of geranylgeranyltransferase, GGTI-286 mimics the effects of statins. indicating geranylgeranylation is key to MPO expression. Reduction of MPO mRNA levels was observed in vivo in leukocytes from statin-fed mice. correlating with reductions in MPO protein and enzyme activity. These findings suggest that the pleiotropic protections afforded by statins may be due in part to suppression of MPO expression. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:442 / 451
页数:10
相关论文
共 71 条
[1]   Nitric oxide is a physiological substrate for mammalian peroxidases [J].
Abu-Soud, HM ;
Hazen, SL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (48) :37524-37532
[2]   Myeloperoxidase polymorphism related to cardiovascular events in coronary artery disease [J].
Asselbergs, FW ;
Reynolds, WF ;
Cohen-Tervaert, JW ;
Jessurun, GAJ .
AMERICAN JOURNAL OF MEDICINE, 2004, 116 (06) :429-430
[3]   Myeloperoxidase serum levels predict risk in patients with acute coronary syndromes [J].
Baldus, S ;
Heeschen, C ;
Meinertz, T ;
Zeiher, AM ;
Eiserich, JP ;
Münzel, T ;
Simoons, ML ;
Hamm, CW .
CIRCULATION, 2003, 108 (12) :1440-1445
[4]   The myeloperoxidase product hypochlorous acid oxidizes HDL in the human artery wall and impairs ABCA1-dependent cholesterol transport [J].
Bergt, C ;
Pennathur, S ;
Fu, XY ;
Byun, J ;
O'Brien, K ;
McDonald, TO ;
Singh, P ;
Anantharamaiah, GM ;
Chait, A ;
Brunzell, J ;
Geary, RL ;
Oram, JF ;
Heinecke, JW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (35) :13032-13037
[5]   Increased atherosclerosis in myeloperoxidase-deficient mice [J].
Brennan, ML ;
Anderson, MM ;
Shih, DM ;
Qu, XD ;
Wang, XP ;
Mehta, AC ;
Lim, LL ;
Shi, WB ;
Hazen, SL ;
Jacob, JS ;
Crowley, JR ;
Heinecke, JW ;
Lusis, AJ .
JOURNAL OF CLINICAL INVESTIGATION, 2001, 107 (04) :419-430
[6]   Mice lacking myeloperoxidase are more susceptible to experimental autoimmune encephalomyelitis [J].
Brennan, ML ;
Gaur, A ;
Pahuja, A ;
Lusis, AJ ;
Reynolds, WF .
JOURNAL OF NEUROIMMUNOLOGY, 2001, 112 (1-2) :97-105
[7]   A screen of candidates from peaks of linkage: evidence for the involvement of myeloperoxidase in multiple sclerosis [J].
Chataway, J ;
Sawcer, S ;
Feakes, R ;
Coraddu, F ;
Broadley, S ;
Jones, HB ;
Clayton, D ;
Gray, J ;
Goodfellow, PN ;
Compston, A .
JOURNAL OF NEUROIMMUNOLOGY, 1999, 98 (02) :208-213
[8]  
Collins R, 2002, INT J CLIN PRACT, V56, P53
[9]   Association between Alzheimer's disease and a functional polymorphism in the myeloperoxidase gene [J].
Crawford, FC ;
Freeman, MJ ;
Schinka, JA ;
Morris, MD ;
Abdullah, LI ;
Richards, D ;
Sevush, S ;
Duara, R ;
Mullan, MJ .
EXPERIMENTAL NEUROLOGY, 2001, 167 (02) :456-459
[10]   MYELOPEROXIDASE, A CATALYST FOR LIPOPROTEIN OXIDATION, IS EXPRESSED IN HUMAN ATHEROSCLEROTIC LESIONS [J].
DAUGHERTY, A ;
DUNN, JL ;
RATERI, DL ;
HEINECKE, JW .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (01) :437-444