Eosinophil granule-derived major basic protein induces IL-8 expression in human intestinal myofibroblasts

被引:17
作者
Furuta, GT
Ackerman, SJ
Varga, J
Spiess, AM
Wang, MY
Wershil, BK
机构
[1] Childrens Hosp, Div Pediat Gastroenterol & Nutr, Combined Program Pediat Gastroenterol & Nutr, Boston, MA 02115 USA
[2] Massachusetts Gen Hosp, Boston, MA 02114 USA
[3] Beth Israel Deaconess Med Ctr, Div Expt Pathol, Boston, MA 02215 USA
[4] Univ Illinois, Coll Med, Dept Med, Rheumatol Sect, Chicago, IL USA
[5] Univ Illinois, Coll Med, Dept Biochem & Mol Biol, Chicago, IL USA
[6] SUNY Hlth Sci Ctr, Brooklyn, NY 11203 USA
关键词
eosinophil IL-8; major basic protein; gastrointestinal; fibroblast;
D O I
10.1046/j.1365-2249.2000.01337.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Eosinophil infiltration occurs in a variety of allergic and inflammatory diseases, The release of preformed mediators From eosinophils may contribute to inflammatory responses. We investigated the ability of eosinophil-derived major basic protein and eosinophil-derived neurotoxin to stimulate production of IL-8 from intestinal myofibroblasts. Intestinal myofibroblasts (18-Co cells) were incubated with major basic protein, eosinophil-derived neurotoxin, or a synthetic analogue of major basic protein, poly-L-arginine. Immunoreactive IL-g was measured by ELISA and IL-8 mRNA levels were analysed by Northern blot or reverse transcription-polymerase chain assay. Major basic protein induced IL-8 mRNA production and release of significant levels of IL-8 immunoreactive protein. By contrast, eosinophil-derived neurotoxin stimulated little IL-8 release. The induction of IL-8 mRNA by poly-L-arginine was significantly inhibited by actinomycin D. These findings demonstrate a novel interaction between eosinophils and intestinal fibroblasts that may be involved in the pathogenesis of diseases associated with tissue eosinophilia.
引用
收藏
页码:35 / 40
页数:6
相关论文
共 45 条
[1]  
ABUGHAZALEH RI, 1992, J MEMBRANE BIOL, V128, P153
[2]  
ABUGHAZALEH RI, 1989, J IMMUNOL, V142, P2393
[3]  
ACKERMAN SJ, 1983, J IMMUNOL, V131, P2977
[4]   ACIDIC POLYAMINO ACIDS INHIBIT HUMAN EOSINOPHIL GRANULE MAJOR BASIC-PROTEIN TOXICITY - EVIDENCE OF A FUNCTIONAL-ROLE FOR PROMBP [J].
BARKER, RL ;
GUNDEL, RH ;
GLEICH, GJ ;
CHECKEL, JL ;
LOEGERING, DA ;
PEASE, LR ;
HAMANN, KJ .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 88 (03) :798-805
[5]   HUMAN EOSINOPHILS STIMULATE DNA-SYNTHESIS AND MATRIX PRODUCTION IN DERMAL FIBROBLASTS [J].
BIRKLAND, TP ;
CHEAVENS, MD ;
PINCUS, SH .
ARCHIVES OF DERMATOLOGICAL RESEARCH, 1994, 286 (06) :312-318
[6]   Quantification of inflammatory mediators in stool samples of patients with inflammatory bowel disorders and controls [J].
Bischoff, SC ;
Grabowsky, J ;
Manns, MP .
DIGESTIVE DISEASES AND SCIENCES, 1997, 42 (02) :394-403
[7]  
BUTTERFIELD JH, 1990, LAB INVEST, V62, P77
[8]   ACTIVATED EOSINOPHILS IN ADULT CELIAC-DISEASE - EVIDENCE FOR A LOCAL RELEASE OF MAJOR BASIC-PROTEIN [J].
COLOMBEL, JF ;
TORPIER, G ;
JANIN, A ;
KLEIN, O ;
CORTOT, A ;
CAPRON, M .
GUT, 1992, 33 (09) :1190-1194
[9]   HUMAN EOSINOPHIL GRANULE MAJOR BASIC-PROTEIN AND SYNTHETIC POLYCATIONS INDUCE AIRWAY HYPERRESPONSIVENESS IN-VIVO DEPENDENT ON BRADYKININ GENERATION [J].
COYLE, AJ ;
ACKERMAN, SJ ;
BURCH, R ;
PROUD, D ;
IRVIN, CG .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (04) :1735-1740
[10]   CATIONIC PROTEIN-INDUCED SENSORY NERVE ACTIVATION - ROLE OF SUBSTANCE-P IN AIRWAY HYPERRESPONSIVENESS AND PLASMA-PROTEIN EXTRAVASATION [J].
COYLE, AJ ;
PERRETTI, F ;
MANZINI, S ;
IRVIN, CG .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (06) :2301-2306