Interleukin-8 production by macrophages from atheromatous plaques

被引:139
作者
Apostolopoulos, J
Davenport, P
Tipping, PG
机构
[1] Centre for Inflammatory Diseases, Monash Univ. Department of Medicine, Monash Medical Centre, Victoria
[2] Department of Medicine, Monash Medical Centre, Clayton, Vic. 3168
关键词
interleukin-8; atherosclerosis; macrophage; human;
D O I
10.1161/01.ATV.16.8.1007
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Interleukin-8 (IL-8) is a chemotactic peptide produced by macrophages that may be involved in the recruitment of inflammatory cells into atherosclerotic plaques. In vitro, IL-8 production by macrophages isolated from carotid plaques (1240+/-510 pg . 10(5) cells(-1). 24 h(-1), mean+/-SEM, n=6) and noncarotid plaques (4312+/-1588 pg . 10(5) cells(-1). 24 h(-1), n=9) was significantly greater than IL-8 production by blood monocytes isolated from the same patients (526+/-278 pg . 10(5) cells(-1). 24 h(-1), n=6, P<.05 and 726+/-384 pg . 10(5) cells(-1). 24 h(-1), n=9, P<.01, respectively). IL-8 produced by atherosclerotic macrophages was demonstrated to be biologically active in a neutrophil chemotaxis assay. IL-8 mRNA was detectable in plaque macrophages and blood monocytes from these patients, but blood monocytes from normal donors did not exhibit detectable IL-8 mRNA. IL-8 mRNA was localized in macrophage-rich areas of atherosclerotic plaques by in situ hybridization. These studies demonstrate that macrophages from atherosclerotic plaques show an enhanced capacity to produce IL-8 compared with normal and patient blood monocytes and that macrophages are a major site of IL-8 mRNA production in atherosclerotic plaques. These results provide further evidence for a proinflammatory role for macrophages in atherosclerosis.
引用
收藏
页码:1007 / 1012
页数:6
相关论文
共 30 条
[1]  
APOSTOLOPOULOS JJ, 1987, J LIPID RES, V28, P642
[2]   NEUTROPHIL-ACTIVATING PEPTIDE-1 INTERLEUKIN-8, A NOVEL CYTOKINE THAT ACTIVATES NEUTROPHILS [J].
BAGGIOLINI, M ;
WALZ, A ;
KUNKEL, SL .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 84 (04) :1045-1049
[3]  
BARKER JNWN, 1991, AM J PATHOL, V139, P869
[4]   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
[5]  
BOYUM A, 1968, SCAND J CLIN LAB INV, VS 21, P77
[6]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[7]  
CROMWELL O, 1992, IMMUNOLOGY, V77, P330
[8]   A 48-WELL MICRO CHEMOTAXIS ASSEMBLY FOR RAPID AND ACCURATE MEASUREMENT OF LEUKOCYTE MIGRATION [J].
FALK, W ;
GOODWIN, RH ;
LEONARD, EJ .
JOURNAL OF IMMUNOLOGICAL METHODS, 1980, 33 (03) :239-247
[9]   A TECHNIQUE FOR RADIOLABELING DNA RESTRICTION ENDONUCLEASE FRAGMENTS TO HIGH SPECIFIC ACTIVITY [J].
FEINBERG, AP ;
VOGELSTEIN, B .
ANALYTICAL BIOCHEMISTRY, 1983, 132 (01) :6-13
[10]  
FRERING B, 1994, J THORAC CARDIOV SUR, V108, P636