Prostaglandin E-2 synthesis and cyclooxygenase expression in abdominal aortic aneurysms

被引:90
作者
Holmes, DR
Wester, W
Thompson, RW
Reilly, JM
机构
[1] WASHINGTON UNIV, SCH MED, DEPT SURG, ST LOUIS, MO 63110 USA
[2] JOHN COCHORAN VET ADM MED CTR, ST LOUIS, MO USA
关键词
D O I
10.1016/S0741-5214(97)70210-6
中图分类号
R61 [外科手术学];
学科分类号
摘要
Purpose: The purpose of this study was to evaluate the expression of prostaglandin E-2 (PGE(2)) and the two cyclooxygenase isoforms (cox1 and cox2) in human abdominal aortic aneurysm (AAA) tissue. Methods: Ten specimens each of normal aortas and aneurysmal aortas were collected and used for histologic analysis and whole organ culture. An enzyme-linked immunosorbent assay for PGE(2) was performed on the media from the aortic explant whole organ culture. An immunohistochemical analysis for PGE(2) was performed, as was in situ hybridization for cox1 and cox2 on tissue sections. Results: PGE(2) production of AAA specimens was found to be 67,287 +/- 27,303 pg/ml as compared with 1698 +/- 858 pg/ml for normal aortic specimens (p < 0.001). PGE(2) was localized by immunohistochemical analysis to the inflammatory infiltrate in AAAs. Minimal expression was noted in normal aortas. Using in situ hybridization, little expression of cox1 was noted in either the normal or the AAA specimens. Cox2 was expressed by macrophage-like cells within the inflammatory infiltrate of the AAA specimens but was not significantly expressed in the normal aorta. Conclusion: The expression of PGE(2) is associated with the pathogenesis of human AAAs. Its expression is localized to macrophage-like cells within the inflammatory infiltrate and is controlled by the cox2 isoform of cyclooxygenase. Cox2 is, therefore, a potential target for pharmacotherapy of AAAs.
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页码:810 / 815
页数:6
相关论文
共 22 条
[1]   PROINFLAMMATORY CYTOKINES REGULATE CYCLOOXYGENASE-2, MESSENGER-RNA EXPRESSION IN HUMAN MACROPHAGES [J].
ARIASNEGRETE, S ;
KELLER, K ;
CHADEE, K .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 208 (02) :582-589
[2]  
Brophy C M, 1991, Ann Vasc Surg, V5, P229, DOI 10.1007/BF02329378
[3]   ELASTIN DEGRADATION IN ABDOMINAL AORTIC-ANEURYSMS [J].
CAMPA, JS ;
GREENHALGH, RM ;
POWELL, JT .
ATHEROSCLEROSIS, 1987, 65 (1-2) :13-21
[4]  
CORCORAN ML, 1992, J BIOL CHEM, V267, P515
[5]  
FLETCHER BS, 1992, J BIOL CHEM, V267, P4338
[6]   CONNECTIVE-TISSUE PROTEINASES AND INHIBITORS IN ABDOMINAL AORTIC-ANEURYSMS - INVOLVEMENT OF THE VASA VASORUM IN THE PATHOGENESIS OF AORTIC-ANEURYSMS [J].
HERRON, GS ;
UNEMORI, E ;
WONG, M ;
RAPP, JH ;
HIBBS, MH ;
STONEY, RJ .
ARTERIOSCLEROSIS AND THROMBOSIS, 1991, 11 (06) :1667-1677
[7]   HUMAN CYCLOOXYGENASE-2 CDNA [J].
HLA, T ;
NEILSON, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (16) :7384-7388
[8]   Indomethacin prevents elastase-induced abdominal aortic aneurysms in the rat [J].
Holmes, DR ;
Petrinec, D ;
Wester, W ;
Thompson, RW ;
Reilly, JM .
JOURNAL OF SURGICAL RESEARCH, 1996, 63 (01) :305-309
[9]  
JEANCLAUDE J, 1994, SURGERY, V116, P472
[10]  
LEE SH, 1992, J BIOL CHEM, V267, P25934