Inhibition of tumour necrosis factor production in endotoxin-stimulated human mononuclear leukocytes by the prostacyclin analogue iloprost: Cellular mechanisms

被引:47
作者
Jorres, A
Dinter, H
Topley, N
Gahl, GM
Frei, U
Scholz, P
机构
[1] SCHERING AG, D-1000 BERLIN, GERMANY
[2] UNIV WALES COLL MED, INST NEPHROL, CARDIFF CF4 4XN, S GLAM, WALES
关键词
tumour necrosis factor alpha; TNF-alpha inhibition; iloprost; endotoxin;
D O I
10.1006/cyto.1996.0145
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The prostacyclin analogue iloprost has been shown to inhibit effectively TNF-alpha production in human peripheral blood mononuclear leukocytes (PBMC) stimulated with bacterial lipopolysaccharide (LPS). The current paper set out to analyse further the possible mechanisms involved in the regulation of TNF-alpha synthesis by iloprost, Healthy human PBMC were challenged with Escherichia coli LPS and assessed for TNF-alpha gene transcription, mRNA stability and protein secretion, Iloprost reduced both steady-state TNF-alpha mRNA expression and protein release as assessed by Northern blot analysis, polymerase chain reaction and enzyme immunoassay, This effect was related both to a reduction of TNF-alpha transcriptional activity (as evaluated by nuclear run-on transcription analysis) and a decrease in TNF-alpha mRNA stability (as assessed by serial Northern blot analysis of TNF-alpha mRNA content in PBMC blocked with actinomycin D). When collectively assessed, these data demonstrate that iloprost regulates TNF-alpha synthesis at both transcriptional and post-transcriptional level. (C) 1997 Academic Press Limited.
引用
收藏
页码:119 / 125
页数:7
相关论文
共 28 条
[1]   COMPARISON OF ILOPROST, CICAPROST AND PROSTACYCLIN EFFECTS ON CYCLIC-AMP METABOLISM IN INTACT PLATELETS [J].
ASHBY, B .
PROSTAGLANDINS, 1992, 43 (03) :255-261
[2]   PROTECTION AGAINST ENDOTOXIC-SHOCK BY A TUMOR-NECROSIS-FACTOR RECEPTOR IMMUNOADHESIN [J].
ASHKENAZI, A ;
MARSTERS, SA ;
CAPON, DJ ;
CHAMOW, SM ;
FIGARI, IS ;
PENNICA, D ;
GOEDDEL, DV ;
PALLADINO, MA ;
SMITH, DH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (23) :10535-10539
[3]   ASSAY OF A RIBONUCLEASE THAT PREFERENTIALLY HYDROLYSES MESSENGER-RNAS CONTAINING CYTOKINE-DERIVED UA-RICH INSTABILITY SEQUENCES [J].
BEUTLER, B ;
THOMPSON, P ;
KEYES, J ;
HAGERTY, K ;
CRAWFORD, D .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1988, 152 (03) :973-980
[4]   CONTROL OF CACHECTIN (TUMOR-NECROSIS-FACTOR) SYNTHESIS - MECHANISMS OF ENDOTOXIN RESISTANCE [J].
BEUTLER, B ;
KROCHIN, N ;
MILSARK, IW ;
LUEDKE, C ;
CERAMI, A .
SCIENCE, 1986, 232 (4753) :977-980
[5]  
BEUTLER B, 1989, ANNU REV IMMUNOL, V7, P625, DOI 10.1146/annurev.iy.07.040189.003205
[6]   IDENTIFICATION OF A COMMON NUCLEOTIDE-SEQUENCE IN THE 3'-UNTRANSLATED REGION OF MESSENGER-RNA MOLECULES SPECIFYING INFLAMMATORY MEDIATORS [J].
CAPUT, D ;
BEUTLER, B ;
HARTOG, K ;
THAYER, R ;
BROWNSHIMER, S ;
CERAMI, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (06) :1670-1674
[7]  
EMERSON TE, 1992, CIRC SHOCK, V38, P75
[8]  
ENDRES S, 1991, IMMUNOLOGY, V72, P56
[9]  
FRENDSCHO MH, 1994, J IMMUNOL, V152, P1347
[10]   INHIBITION OF ENDOTOXIN-INDUCED MACROPHAGE TUMOR-NECROSIS-FACTOR EXPRESSION BY A PROSTACYCLIN ANALOG AND ITS BENEFICIAL EFFECT IN EXPERIMENTAL LIPOPOLYSACCHARIDE INTOXICATION [J].
GRUNDMANN, HJ ;
HAHNLE, U ;
HEGENSCHEID, B ;
SAHLMULLER, G ;
BIENZLE, U ;
BLITSTEINWILLINGER, E .
JOURNAL OF INFECTIOUS DISEASES, 1992, 165 (03) :501-505