CYTOKINE MESSENGER-RNA EXPRESSION IN INTESTINE FROM NORMAL AND INFLAMMATORY BOWEL-DISEASE PATIENTS

被引:79
作者
MCCABE, RP
SECRIST, H
BOTNEY, M
EGAN, M
PETERS, MG
机构
[1] Department of Medicine, Washington University School Medicine, St. Louis
来源
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY | 1993年 / 66卷 / 01期
关键词
D O I
10.1006/clin.1993.1007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Cytokines are involved in the regulation of normal immune events and may be important in the development or perpetuation of immune events in inflammatory bowel disease. We have previously shown that normal human mononuclear cells from tonsil, spleen, and peripheral blood exhibit tissue and stimulus-specific patterns of cytokine mRNA expression. The aim of this study was to determine if disease-dependent differences of cytokine mRNA expression could be found in the intestine. Total RNA was isolated from intestinal mucosa and lamina propria mononuclear cells from inflammatory bowel disease patients and controls. cDNA probes specific for interleukin (IL)-1, -4, -5, and -6 and transforming growth factor-β were used. IL-1β mRNA and TGF-β mRNA steady state expressions were higher in inflammatory bowel disease specimens than in normal intestine. In addition, mononuclear cell specimens had stronger cytokine mRNA expression than mucosal specimens. The steady state mRNA expression of proinflammatory cytokines is higher in inflammatory bowel disease, consistent with the ongoing inflammation seen. © 1993 Academic Press, Inc.
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收藏
页码:52 / 58
页数:7
相关论文
共 34 条
[1]   ACTIVATION OF MONOCYTES DURING INFLAMMATORY BOWEL-DISEASE [J].
ANDUS, T ;
GROSS, V ;
CASAR, I ;
KRUMM, D ;
HOSP, J ;
DAVID, M ;
SCHOLMERICH, J .
PATHOBIOLOGY, 1991, 59 (03) :166-170
[2]   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
[3]   TRANSFORMING GROWTH FACTOR-BETA-1 IS DECREASED IN REMODELING HYPERTENSIVE BOVINE PULMONARY-ARTERIES [J].
BOTNEY, MD ;
PARKS, WC ;
CROUCH, EC ;
STENMARK, K ;
MECHAM, RP .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 89 (05) :1629-1635
[4]   ISOLATION AND FUNCTIONAL CHARACTERIZATION OF HUMAN INTESTINAL MUCOSAL LYMPHOID-CELLS [J].
BULL, DM ;
BOOKMAN, MA .
JOURNAL OF CLINICAL INVESTIGATION, 1977, 59 (05) :966-974
[5]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[6]   TRANSFORMING GROWTH FACTOR-BETA SPECIFICALLY ENHANCES IGA PRODUCTION BY LIPOPOLYSACCHARIDE-STIMULATED MURINE LYMPHOCYTES-B [J].
COFFMAN, RL ;
LEBMAN, DA ;
SHRADER, B .
JOURNAL OF EXPERIMENTAL MEDICINE, 1989, 170 (03) :1039-1044
[7]   INTERLEUKIN-1 (IL-1) GENE-EXPRESSION, SYNTHESIS, AND EFFECT OF SPECIFIC IL-1 RECEPTOR BLOCKADE IN RABBIT IMMUNE-COMPLEX COLITIS [J].
COMINELLI, F ;
NAST, CC ;
CLARK, BD ;
SCHINDLER, R ;
LLERENA, R ;
EYSSELEIN, VE ;
THOMPSON, RC ;
DINARELLO, CA .
JOURNAL OF CLINICAL INVESTIGATION, 1990, 86 (03) :972-980
[8]   HUMAN TRANSFORMING GROWTH FACTOR-BETA COMPLEMENTARY-DNA SEQUENCE AND EXPRESSION IN NORMAL AND TRANSFORMED-CELLS [J].
DERYNCK, R ;
JARRETT, JA ;
CHEN, EY ;
EATON, DH ;
BELL, JR ;
ASSOIAN, RK ;
ROBERTS, AB ;
SPORN, MB ;
GOEDDEL, DV .
NATURE, 1985, 316 (6030) :701-705
[9]  
DINARELLO CA, 1991, BLOOD, V77, P1627
[10]   CLONING AND SEQUENCE-ANALYSIS OF CDNA FOR HUMAN CATHEPSIN-D [J].
FAUST, PL ;
KORNFELD, S ;
CHIRGWIN, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (15) :4910-4914