TRANSFORMING GROWTH-FACTOR-BETA OPPOSES THE STIMULATORY EFFECTS OF INTERLEUKIN-1 AND TUMOR-NECROSIS-FACTOR ON AMNION CELL PROSTAGLANDIN-E2 PRODUCTION - IMPLICATION FOR PRETERM LABOR

被引:46
作者
BRY, K [1 ]
HALLMAN, M [1 ]
机构
[1] UNIV HELSINKI, DEPT PEDIAT, SF-00100 HELSINKI 10, FINLAND
关键词
PRETERM LABOR; PROSTAGLANDINS; INTERLEUKIN-1; TUMOR NECROSIS FACTOR; TRANSFORMING GROWTH FACTOR-BETA; FETAL MEMBRANES;
D O I
10.1016/S0002-9378(11)91662-7
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
OBJECTIVE: In preterm labor increased concentrations of interleukin-1 and tumor necrosis factor are present in amniotic fluid. These cytokines may promote labor by stimulating the production of prostaglandins by intrauterine tissues. In many biologic processes, transforming growth factor-beta modifies the actions of cytokines. We studied the effect of transforming growth factor-beta on the cytokine-induced prostaglandin E2 production by amnion cells. STUDY DESIGN: Human amnion cells in monolayer culture were treated with interleukin-1, tumor necrosis factor, or vehicle in the presence or absence of transforming growth factor-beta. The prostaglandin E2 production was measured. RESULTS: Transforming growth factor-beta decreased the interleukin-1- or tumor necrosis factor-induced prostaglandin E2 production by 70% to 80% and the basal prostaglandin E2 synthesis by 27%. The synergistic stimulation of prostaglandin E2 production by the combination of interleukin-1 with tumor necrosis factor was inhibited by 80% in cells treated with transforming growth factor-beta. Transforming growth factor-beta-1, -beta-2, and -beta-1,2 were equipotent. CONCLUSION: Transforming growth factor-beta suppresses the cytokine-induced prostaglandin E2 production by amnion cells and may be an important factor in maintaining pregnancy in the face of labor-promoting cytokines.
引用
收藏
页码:222 / 226
页数:5
相关论文
共 29 条
[1]   EXTRACELLULAR-MATRIX COMPONENTS SYNTHESIZED BY HUMAN AMNIOTIC EPITHELIAL-CELLS IN CULTURE [J].
ALITALO, K ;
KURKINEN, M ;
VAHERI, A ;
KRIEG, T ;
TIMPL, R .
CELL, 1980, 19 (04) :1053-1062
[2]   A TRANSFORMING GROWTH-FACTOR-BETA-2 (TGF-BETA-2)-LIKE IMMUNOSUPPRESSIVE FACTOR IN AMNIOTIC-FLUID AND LOCALIZATION OF TGF-BETA-2 MESSENGER-RNA IN THE PREGNANT UTERUS [J].
ALTMAN, DJ ;
SCHNEIDER, SL ;
THOMPSON, DA ;
CHENG, HL ;
TOMASI, TB .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 172 (05) :1391-1401
[3]   TRANSFORMING GROWTH FACTOR-BETA INHIBITS PROSTAGLANDIN PRODUCTION IN AMNION AND A431 CELLS [J].
BERCHUCK, A ;
MACDONALD, PC ;
MILEWICH, L ;
CASEY, ML .
PROSTAGLANDINS, 1989, 38 (04) :453-464
[4]   SYNERGISTIC STIMULATION OF AMNION CELL PROSTAGLANDIN-E2 SYNTHESIS BY INTERLEUKIN-1, TUMOR-NECROSIS-FACTOR AND PRODUCTS FROM ACTIVATED HUMAN GRANULOCYTES [J].
BRY, K ;
HALLMAN, M .
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS, 1991, 44 (04) :241-245
[5]   CACHECTIN TUMOR NECROSIS FACTOR-ALPHA FORMATION IN HUMAN DECIDUA - POTENTIAL ROLE OF CYTOKINES IN INFECTION-INDUCED PRETERM LABOR [J].
CASEY, ML ;
COX, SM ;
BEUTLER, B ;
MILEWICH, L ;
MACDONALD, PC .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 83 (02) :430-436
[6]   CHARACTERIZATION OF PROSTAGLANDIN FORMATION BY HUMAN AMNION CELLS IN MONOLAYER-CULTURE [J].
CASEY, ML ;
MACDONALD, PC ;
MITCHELL, MD .
PROSTAGLANDINS, 1984, 27 (03) :421-427
[7]   BIOMOLECULAR PROCESSES IN THE INITIATION OF PARTURITION - DECIDUAL ACTIVATION [J].
CASEY, ML ;
MACDONALD, PC .
CLINICAL OBSTETRICS AND GYNECOLOGY, 1988, 31 (03) :533-552
[8]  
CLARK DA, 1990, J IMMUNOL, V144, P3008
[9]  
DIAZ A, 1989, J BIOL CHEM, V264, P11554
[10]   FLUOROMETRIC QUANTIFICATION OF DNA IN CELLS AND TISSUE [J].
DOWNS, TR ;
WILFINGER, WW .
ANALYTICAL BIOCHEMISTRY, 1983, 131 (02) :538-547