Endothelial responses to oxidized lipoproteins determine genetic susceptibility to atherosclerosis in mice

被引:154
作者
Shi, WB
Haberland, ME
Jien, ML
Shih, DM
Lusis, AJ
机构
[1] Univ Calif Los Angeles, Sch Med, Dept Med, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Microbiol & Mol Genet, Los Angeles, CA 90024 USA
[3] Univ Calif Los Angeles, Dept Physiol Sci, Los Angeles, CA 90024 USA
关键词
endothelium; cells; atherosclerosis; lipoproteins; mice;
D O I
10.1161/01.CIR.102.1.75
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-Oxidized LDL has been found within the subendothelial space, and it exhibits numerous atherogenic properties, including induction of inflammatory genes. We examined the possibility that variations in endothelial response to minimally modified LDL (MM-LDL) constitute one of the genetic components in atherosclerosis, Methods and Results-By a novel explant technique, endothelial cells (ECs) were isolated from the aorta of inbred mouse strains with different susceptibilities to diet-induced atherosclerosis. Responses to MM-LDL were evaluated by examining the expression of inflammatory genes involved in atherosclerosis, including monocyte chemotactic protein-1 (MCP-1) and macrophage-colony-stimulating factor (M-CSF), an oxidative stress gene, heme oxygenase-1 (HO-1), and other, noninflammatory, genes. ECs from the susceptible mouse strain C57BL/6J exhibited dramatic induction of MCP-1, M-CSF, and HO-1, whereas ECs from the resistant strain C3H/HeJ showed little or no induction. In contrast, ECs from the 2 strains responded similarly to lipopolysaccharide. Conclusions-These data provide strong evidence that genetic factors in atherosclerosis act at the level of the vessel wall.
引用
收藏
页码:75 / 81
页数:7
相关论文
共 46 条
[1]   HUMAN MACROPHAGE METABOLISM OF LOW-DENSITY-LIPOPROTEIN OXIDIZED BY STIMULATED NEUTROPHILS AND FERRITIN [J].
ABDALLA, DSP ;
COSTAROSA, LFBP ;
MONTEIRO, HP ;
CAMPA, A ;
CURI, R .
ATHEROSCLEROSIS, 1994, 107 (02) :157-163
[2]   ATHEROSCLEROSIS - BASIC MECHANISMS - OXIDATION, INFLAMMATION, AND GENETICS [J].
BERLINER, JA ;
NAVAB, M ;
FOGELMAN, AM ;
FRANK, JS ;
DEMER, LL ;
EDWARDS, PA ;
WATSON, AD ;
LUSIS, AJ .
CIRCULATION, 1995, 91 (09) :2488-2496
[3]   MINIMALLY MODIFIED LOW-DENSITY-LIPOPROTEIN STIMULATES MONOCYTE ENDOTHELIAL INTERACTIONS [J].
BERLINER, JA ;
TERRITO, MC ;
SEVANIAN, A ;
RAMIN, S ;
KIM, JA ;
BAMSHAD, B ;
ESTERSON, M ;
FOGELMAN, AM .
JOURNAL OF CLINICAL INVESTIGATION, 1990, 85 (04) :1260-1266
[4]   Decreased lesion formation in CCR2-/- mice reveals a role for chemokines in the initiation of atherosclerosis [J].
Boring, L ;
Gosling, J ;
Cleary, M ;
Charo, IF .
NATURE, 1998, 394 (6696) :894-897
[6]  
Chisolm GM, 1991, CLIN CARDIOL, V14, P125
[7]  
CLINTON SK, 1992, AM J PATHOL, V140, P301
[8]   MINIMALLY MODIFIED LOW-DENSITY-LIPOPROTEIN INDUCES MONOCYTE CHEMOTACTIC PROTEIN-1 IN HUMAN ENDOTHELIAL-CELLS AND SMOOTH-MUSCLE CELLS [J].
CUSHING, SD ;
BERLINER, JA ;
VALENTE, AJ ;
TERRITO, MC ;
NAVAB, M ;
PARHAMI, F ;
GERRITY, R ;
SCHWARTZ, CJ ;
FOGELMAN, AM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (13) :5134-5138
[9]   Association between serum amyloid a proteins and coronary artery disease - Evidence from two distinct arteriosclerotic processes [J].
Fyfe, AI ;
Rothenberg, LS ;
DeBeer, FC ;
Cantor, RM ;
Rotter, JI ;
Lusis, AJ .
CIRCULATION, 1997, 96 (09) :2914-2919
[10]   Analysis of macrophage scavenger receptor (SR-A) expression in human aortic atherosclerotic lesions [J].
Gough, PJ ;
Greaves, DR ;
Suzuki, H ;
Hakkinen, T ;
Hiltunen, MO ;
Turunen, M ;
Herttuala, SY ;
Kodama, T ;
Gordon, S .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1999, 19 (03) :461-471