Scavenger receptors: Implications in atherothrombotic disorders

被引:37
作者
Ashraf, Mohammad Z. [1 ]
Gupta, Neha [1 ]
机构
[1] Def Inst Physiol & Allied Sci, Cellular Biochem & Genom Div, Delhi 110054, India
关键词
Scavenger receptors; Atherosclerosis; Thrombosis; Platelets; CD36; SR-BI; LOW-DENSITY-LIPOPROTEIN; B TYPE-I; ATHEROSCLEROTIC LESION DEVELOPMENT; MARROW-DERIVED CELLS; E-DEFICIENT MICE; SR-BI; OXIDIZED PHOSPHOLIPIDS; PLATELET ACTIVATION; CD36; EXPRESSION;
D O I
10.1016/j.biocel.2011.01.019
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
Scavenger receptors are modified lipoprotein binding receptors, expressed on the surface of a variety of cells including endothelial, macrophages and platelets. The most extensively studied class B scavenger receptors comprise of CD36 and SR-BI and have been found to bind to native and modified LDL Interaction of modified LDL to CD36 accelerates foam cell formation, the key step in atherosclerotic plaque deposition. Recently scavenger receptors have also been implicated in thrombosis. Platelet CD36 serves as a sensor of oxidative stress and modulator of platelet reactivity under hyperlipidemic conditions thus, inducing prothrombotic signals. In contrast, targeting platelet SR-BI corresponds to reduce platelet hyper-reactivity in hyperlipidemia suggesting that targeting these receptors could be a promising strategy for the treatment of atherothrombotic disorders. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:697 / 700
页数:4
相关论文
共 30 条
[1]  
ACTON SL, 1994, J BIOL CHEM, V269, P21003
[2]   Specific oxidized phospholipids inhibit scavenger receptor BI-mediated selective uptake of cholesteryl esters [J].
Ashraf, Mohammad Z. ;
Kar, Niladri S. ;
Chen, Xi ;
Choi, Jaewoo ;
Salomon, Robert G. ;
Febbraio, Maria ;
Podrez, Eugene A. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (16) :10408-10414
[3]   Loss of SR-BI expression leads to the early onset of occlusive atherosclerotic coronary artery disease, spontaneous myocardial infarctions, severe cardiac dysfunction, and premature death in apolipoprotein E-deficient mice [J].
Braun, A ;
Trigatti, BL ;
Post, MJ ;
Sato, K ;
Simons, M ;
Edelberg, JM ;
Rosenberg, RD ;
Schrenzel, M ;
Krieger, M .
CIRCULATION RESEARCH, 2002, 90 (03) :270-276
[4]   A specific CD36-dependent signaling pathway is required for platelet activation by oxidized low-density lipoprotein [J].
Chen, Kan ;
Febbraio, Maria ;
Li, Wei ;
Silverstein, Roy L. .
CIRCULATION RESEARCH, 2008, 102 (12) :1512-1519
[5]   CLA-1/SR-BI is expressed in atherosclerotic lesion macrophages and regulated by activators of peroxisome proliferator-activated receptors [J].
Chinetti, G ;
Gbaguidi, FG ;
Griglio, S ;
Mallat, Z ;
Antonucci, M ;
Poulain, P ;
Chapman, J ;
Fruchart, JC ;
Tedgui, A ;
Najib-Fruchart, J ;
Staels, B .
CIRCULATION, 2000, 101 (20) :2411-2417
[6]   Scavenger receptor class B type I-mediated protection against atherosclerosis in LDL receptor-negative mice involves its expression in bone marrow-derived cells [J].
Covey, SD ;
Krieger, M ;
Wang, W ;
Penman, M ;
Trigatti, BL .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2003, 23 (09) :1589-1594
[7]   Thrombocytopenia and platelet abnormalities in high-density lipoprotein receptor-deficient mice [J].
Dole, Vandana S. ;
Matuskova, Jana ;
Vasile, Eliza ;
Yesilaltay, Ayce ;
Bergmeier, Wolfgang ;
Bernimoulin, Michael ;
Wagner, Denisa D. ;
Krieger, Monty .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2008, 28 (06) :1111-1116
[8]  
ENDEMANN G, 1993, J BIOL CHEM, V268, P11811
[9]   Platelet CD36 mediates interactions with endothelial cell-derived microparticles and contributes to thrombosis in mice [J].
Ghosh, Arunima ;
Li, Wei ;
Febbraio, Maria ;
Espinola, Ricardo G. ;
McCrae, Keith R. ;
Cockrell, Erin ;
Silverstein, Roy L. .
JOURNAL OF CLINICAL INVESTIGATION, 2008, 118 (05) :1934-1943
[10]  
Hirano K, 1999, CIRC RES, V85, P108