Oxidative stress increases the expression of the CD36 scavenger receptor and the cellular uptake of oxidized low-density lipoprotein in macrophages from atherosclerotic mice: protective role of antioxidants and of paraoxonase

被引:122
作者
Fuhrman, B
Volkova, N
Aviram, M [1 ]
机构
[1] Technion Israel Inst Technol, Rappaport Family Inst Res Med Sci, Lipid Res Lab, IL-31096 Haifa, Israel
[2] Rambam Med Ctr, IL-31096 Haifa, Israel
关键词
oxidative stress; macrophages; oxidized low-density lipoprotein; CD36 scavenger receptor; antioxidants;
D O I
10.1016/S0021-9150(01)00646-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Little is known about the effects of oxidative stress on macropbage lipid peroxidation and on their atherogenic consequences. Therefore, we questioned the causal relationship between cellular lipid peroxides content and macrophagc uptake of oxidized low-density lipoprotein (Ox-LDL). Lipid peroxide content in mouse peritoneal macrophages (MPMs) from E-deficient (E-0) mice increased progressively by up to 4.6 fold during mice aging, and this was accompanied by an age-dependent increase in the cellular uptake of Ox-LDL (90%), and in the expression of the scavenger receptor CD36 mRNA (41%). Inhibition or stimulation of cellular oxidative stress by administration of dietary potent antioxidants (vitamin E or glabridin) or by inducing cellular glutathione depletion (by using buthionine sulfoximine), respectively, resulted in a significant increment or inhibition of macropbage uptake of Ox-LDL and in cellular CD36) mRNA expression, respectively. Intraperitoneal injection of human serum paraoxonase (PON1) into E-0 mice, resulted in a 40-65% decrement in the lipid peroxide content in MPM harvested from E-0 mice at 2-5 months of age, which subsequently resulted in. a similar reduced uptake of Ox-LDL and expression of CD36 mRNA (by 30-40%). In conclusion, our results are the first to demonstrate that macropliage lipid peroxidation stimulates CD36 mRNA expression and enhances the cellular uptake of Ox-LDL. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:307 / 316
页数:10
相关论文
共 36 条
[1]  
ACTON SL, 1994, J BIOL CHEM, V269, P21003
[2]   LDL oxidation by arterial wall macrophages depends on the oxidative status in the lipoprotein and in the cells: Role of prooxidants vs. antioxidants [J].
Aviram, M ;
Fuhrman, B .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 1998, 188 (1-2) :149-159
[3]   PLASMA-LIPOPROTEIN SEPARATION BY DISCONTINUOUS DENSITY GRADIENT ULTRA-CENTRIFUGATION IN HYPERLIPOPROTEINEMIC PATIENTS [J].
AVIRAM, M .
BIOCHEMICAL MEDICINE, 1983, 30 (01) :111-118
[4]   Human serum paraoxonases (PON1) Q and R selectively decrease lipid peroxides in human coronary and carotid atherosclerotic lesions - PON1 esterase and peroxidase-like activities [J].
Aviram, M ;
Hardak, E ;
Vaya, J ;
Mahmood, S ;
Milo, S ;
Hoffman, A ;
Billicke, S ;
Draganov, D ;
Rosenblat, M .
CIRCULATION, 2000, 101 (21) :2510-2517
[5]  
Aviram M, 1996, EUR J CLIN CHEM CLIN, V34, P599
[6]   Activation of NADPH oxidase is required for macrophage-mediated oxidation of low-density lipoprotein [J].
Aviram, M ;
Rosenblat, M ;
Etzioni, A ;
Levy, R .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1996, 45 (09) :1069-1079
[7]   Paraoxonase inhibits high-density lipoprotein oxidation and preserves its functions - A possible peroxidative role for paraoxonase [J].
Aviram, M ;
Rosenblat, M ;
Bisgaier, CL ;
Newton, RS ;
Primo-Parmo, SL ;
La Du, BN .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (08) :1581-1590
[8]  
Aviram M, 2001, METHOD ENZYMOL, V335, P244
[9]  
Aviram M, 2000, FREE RADICAL RES, V33, pS85
[10]   Macrophage Foam Cell Formation During Early Atherogenesis Is Determined by the Balance Between Pro-Oxidants and Anti-Oxidants in Arterial Cells and Blood Lipoproteins [J].
Aviram, Michael .
ANTIOXIDANTS & REDOX SIGNALING, 1999, 1 (04) :585-594