CYTOKINE GENE-EXPRESSION IN AORTIC ADVENTITIAL INFLAMMATION ASSOCIATED WITH ADVANCED ATHEROSCLEROSIS (CHRONIC PERIAORTITIS)

被引:72
作者
RAMSHAW, AL
ROSKELL, DE
PARUMS, DV
机构
[1] HAMMERSMITH HOSP, ROYAL POSTGRAD MED SCH, DEPT HISTOPATHOL, LONDON W12 0NN, ENGLAND
[2] JOHN RADCLIFFE HOSP, NUFFIELD DEPT PATHOL & BACTERIOL, OXFORD OX3 9DU, ENGLAND
关键词
D O I
10.1136/jcp.47.8.721
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Aims-To determine whether aortic adventitial chronic inflammation associated with advanced atherosclerosis (''chronic periaortitis'') is associated with any detectable cytokine gene expression. Methods-RNA was extracted from six fresh surgical specimens of atherosclertic aortic aneurysm wall showing a spectrum of chronic periaortitis. Controls included four normal aortas and an HUT 78 T cell line. Reverse transcriptase and the polymerase chain reaction (PCR) were used to amplify mRNA for interleukins-1 alpha (IL-1 alpha), -2 (IL-2), -4 (IL-4), IL-2 receptor-alpha (IL-2R-alpha), tumour necrosis factor alpha (TNF-alpha) and gamma interferon (IFN-gamma) with beta-actin as an internal control. Results-No TNF-alpha mRNA was detected in any of the inflamed aortic tissue samples, in contrast to the aortic T lymphocytes propagated in culture in IL-2 conditioned medium (aortic cultured T cells) and peripheral blood mononuclear cells from these patients. In contrast, IFN-gamma, IL-1 alpha, IL-2, IL-2 receptor and IL-4 PCR products were detected for each inflamed aortic tissue RNA sample with IFN-gamma mRNA expression increasing with increasing degrees of adventitial inflammation. Only beta-actin mRNA was present in the normal aorta. Conclusions-These findings indicate the active nature of aortic adventitial chronic inflammation associated with human advanced atherosclerosis (''chronic periaortitis'') and show its possible progressive potential to the clinically important diseases termed ''idiopathic retroperitoneal fibrosis'' and ''inflammatory aneurysm''.
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页码:721 / 727
页数:7
相关论文
共 46 条
[1]   CYTOKINES - COORDINATORS OF IMMUNE AND INFLAMMATORY RESPONSES [J].
ARAI, K ;
LEE, F ;
MIYAJIMA, A ;
MIYATAKE, S ;
ARAI, N ;
YOKOTA, T .
ANNUAL REVIEW OF BIOCHEMISTRY, 1990, 59 :783-836
[2]  
Balkwill F.R., 1991, CYTOKINES PRACTICAL
[3]  
BRENNAN F M, 1991, British Journal of Rheumatology, V30, P76
[4]  
BRENNER CA, 1989, BIOTECHNIQUES, V7, P1096
[5]  
BROWN KA, 1988, BRIT J RHEUMATOL, V27, P150
[6]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[7]  
CLINTON SK, 1992, ARCH PATHOL LAB MED, V116, P1292
[8]   IMMUNOENZYMATIC LABELING OF MONOCLONAL-ANTIBODIES USING IMMUNE-COMPLEXES OF ALKALINE-PHOSPHATASE AND MONOCLONAL ANTI-ALKALINE PHOSPHATASE (APAAP COMPLEXES) [J].
CORDELL, JL ;
FALINI, B ;
ERBER, WN ;
GHOSH, AK ;
ABDULAZIZ, Z ;
MACDONALD, S ;
PULFORD, KAF ;
STEIN, H ;
MASON, DY .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1984, 32 (02) :219-229
[9]   DIFFERENTIATION OF T-CELL LYMPHOKINE GENE-EXPRESSION - THE INVITRO ACQUISITION OF T-CELL MEMORY [J].
EHLERS, S ;
SMITH, KA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 173 (01) :25-36
[10]  
ERBER WN, 1984, LANCET, V1, P1042