Interleukin-1 increases fibronectin production by cultured rat cardiac fibroblasts

被引:16
作者
Fernández, L
Mosquera, JA
机构
[1] Univ Zulia, Inst Invest Clin Dr Amer Negrette, Fac Med, Maracaibo, Venezuela
[2] Univ Zulia, Ctr Cirugia Expt, Maracaibo, Venezuela
关键词
fibronectin; fibrosis; cardiac fibroblast; interleukin-1; myocarditis;
D O I
10.1159/000069328
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Objectives: There is evidence of monocyte/macrophage infiltration and increased interleukin (IL)-1 expression, along with increased extracellular matrix (ECM) and fibrosis in the myocardial interstitium, during the course of parasitic, viral and idiopathic myocarditis. The aim of this study was to determine the effect of human and rat IL-1 on the production of fibronectin (FN) by rat cardiac fibroblast cultures. Methods:To test the role of IL-1 in the production of ECM, we determined the FN content in supernatants of rat myocardial fibroblast cultures incubated for 72 h with different doses of human recombinant IL-1 P or with supernatants from lipopolysaccharide (LPS)-stimulated rat macrophage cultures. The content of soluble FN was determined by ELISA. In addition, IL-1beta transcription was also investigated in controls and human recombinant IL-1beta-treated fibroblast cultures. Results:There was a significant, dose-dependent FN-stimulatory effect of recombinant human IL-1beta and LPS-stimulated macrophage-conditioned medium when they were used to stimulate fibroblast cultures. The stimulatory effect on FN production was found to be diminished after treatment of macrophage supernatants with an antibody against rat IL-1. Increased transcription of IL-1beta was found in human recombinant IL-1beta-treated cardiac fibroblasts. Conclusion: Our data suggest that the FN-stimulatory effect of IL-1 on cardiac fibroblasts could be responsible, in part, for interstitial ECM accumulation during the course of myocarditis. Copyright (C) 2003 S. Karger AG, Basel.
引用
收藏
页码:191 / 196
页数:6
相关论文
共 49 条
[1]  
ANDRADE S G, 1986, Memorias do Instituto Oswaldo Cruz, V81, P29, DOI 10.1590/S0074-02761986000100004
[2]   STIMULATION OF RAT MACROPHAGE INTERLEUKIN-1 SECRETION BY PLASMA FIBRONECTIN [J].
BEEZHOLD, DH ;
LAUSE, DB .
IMMUNOLOGICAL INVESTIGATIONS, 1987, 16 (05) :437-449
[3]   Wound repair [J].
Clark, R. A. F. .
CURRENT OPINION IN CELL BIOLOGY, 1989, 1 (05) :1000-1008
[4]   BIOLOGY OF INTERLEUKIN-1 [J].
DINARELLO, CA .
FASEB JOURNAL, 1988, 2 (02) :108-115
[5]  
DINARELLO CA, 1996, NEW ENGL J MED, V328, P106
[6]   REGULATION OF FIBROBLAST PROLIFERATION AND COLLAGEN-SYNTHESIS BY CYTOKINES [J].
FREUNDLICH, B ;
BOMALASKI, JS ;
NEILSON, E ;
JIMENEZ, SA .
IMMUNOLOGY TODAY, 1986, 7 (10) :303-307
[7]   ENZYME-LINKED IMMUNOSORBENT-ASSAY TO QUANTIFY FIBRONECTIN [J].
GOMEZLECHON, MJ ;
CASTELL, JV .
ANALYTICAL BIOCHEMISTRY, 1985, 145 (01) :1-8
[8]   Increased serum concentrations of interleukin-1 beta in patients with coronary artery disease [J].
Hasdai, D ;
Scheinowitz, M ;
Leibovitz, E ;
Sclarovsky, S ;
Eldar, M ;
Barak, V .
HEART, 1996, 76 (01) :24-28
[9]   ISOLATION AND CHARACTERIZATION OF CDNA FROM RENAL TUBULAR EPITHELIUM ENCODING MURINE RANTES [J].
HEEGER, P ;
WOLF, G ;
MEYERS, C ;
SUN, MJ ;
OFARRELL, SC ;
KRENSKY, AM ;
NEILSON, EG .
KIDNEY INTERNATIONAL, 1992, 41 (01) :220-225
[10]   INDUCTION OF INTERLEUKIN-1-BETA MESSENGER-RNA IN ADULT-RAT BRAIN [J].
HIGGINS, GA ;
OLSCHOWKA, JA .
MOLECULAR BRAIN RESEARCH, 1991, 9 (1-2) :143-148