RELATIVE CYTOKINE-STIMULATING ACTIVITIES OF SURFACE COMPONENTS OF THE ORAL PERIODONTOPATHOGENIC BACTERIUM ACTINOBACILLUS-ACTINOMYCETEMCOMITANS

被引:31
作者
REDDI, K
WILSON, M
POOLE, S
MEGHJI, S
HENDERSON, B
机构
[1] UCL EASTMAN DENT INST ORAL HLTH CARE SCI, DEPT MICROBIOL, LONDON WC1X 8LD, ENGLAND
[2] NATL INST BIOL STAND & CONTROLS, POTTERS BAR EN6 3QG, HERTS, ENGLAND
关键词
LPS; CIPDS; A-ACTINOMYCETEMCOMITANS; IL-BETA; IL-6; TNF-ALPHA;
D O I
10.1006/cyto.1995.0072
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 purpose of this study was to determine whether bacterial surface components other than lipopolysaccharide (LPS) could stimulate pro-inflammatory cytokine synthesis by mesenchymal and myelomonocytic cells in vitro. LPS, lipid A-associated proteins (LAP) and saline-extractable surface-associated material (SAM) were isolated from the periodontopathogenic bacterium Actinobacillus actinomycetemcomitans and added to cultures of human gingival fibroblasts (HGFs), human PBMCs and the human myelomonocytic Mono-Mac-6 cell line, Pro-inflammatory cytokine release into culture supernatants was determined by two-site ELISAs. Contrary to expectation, the highly purified LPS extracted from this bacterium was significantly less potent than the other surface extracts in stimulating release of IL-1 beta, IL-6 and TNF-alpha by all three cell types, The SAM was the most potent cytokine-stimulating agent showing equivalent activity to highly purified E. coli LPS in stimulating IL-6 release by PBMCs, LAP also had cytokine-stimulating activity although it was generally significantly less potent than the SAM, Thus in the case of this organism, which is involved in the pathology of chronic inflammatory diseases the LPS does not appear to be the major cytokine-stimulating component. (C) 1995 Academic Press Limited.
引用
收藏
页码:534 / 541
页数:8
相关论文
共 27 条
[1]   INTERLEUKIN-1-BETA PRODUCTION INVIVO AND INVITRO IN RATS AND MICE MEASURED USING SPECIFIC IMMUNORADIOMETRIC ASSAYS [J].
BRISTOW, AF ;
MOSLEY, K ;
POOLE, S .
JOURNAL OF MOLECULAR ENDOCRINOLOGY, 1991, 7 (01) :1-7
[2]  
CAVAILLON J-M, 1990, Cytokine, V2, P313, DOI 10.1016/1043-4666(90)90061-W
[3]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[4]  
Dinarello CA, 1989, INTERLEUKIN 1 INFLAM, P17
[5]   DETERMINING THE VALUE OF A PERIODONTAL DIAGNOSTIC-TEST [J].
DOUGLASS, CW ;
FOX, CH .
JOURNAL OF PERIODONTOLOGY, 1991, 62 (12) :721-730
[6]   COLORIMETRIC METHOD FOR DETERMINATION OF SUGARS AND RELATED SUBSTANCES [J].
DUBOIS, M ;
GILLES, KA ;
HAMILTON, JK ;
REBERS, PA ;
SMITH, F .
ANALYTICAL CHEMISTRY, 1956, 28 (03) :350-356
[7]  
Goldman H.M, 1990, CONT PERIODONTICS
[8]  
HITCHCOCK PJ, 1984, HDB ENDOTOXIN, V1, P339
[9]   ENDOTOXIN-ASSOCIATED PROTEIN - INTERLEUKIN-1-LIKE ACTIVITY ON SERUM AMYLOID-A SYNTHESIS AND LYMPHOCYTE-T ACTIVATION [J].
JOHNS, MA ;
SIPE, JD ;
MELTON, LB ;
STROM, TB ;
MCCABE, WR .
INFECTION AND IMMUNITY, 1988, 56 (06) :1593-1601
[10]   MARGINAL PERIODONTITIS AND CYTOKINES - A REVIEW OF THE LITERATURE [J].
KJELDSEN, M ;
HOLMSTRUP, P ;
BENDTZEN, K .
JOURNAL OF PERIODONTOLOGY, 1993, 64 (11) :1013-1022