SOLUBLE PEPTIDOGLYCAN-INDUCED MONOKINE PRODUCTION CAN BE BLOCKED BY ANTI-CD14 MONOCLONAL-ANTIBODIES AND BY LIPID-A PARTIAL STRUCTURES

被引:159
作者
WEIDEMANN, B
BRADE, H
RIETSCHEL, ET
DZIARSKI, R
BAZIL, V
KUSUMOTO, S
FLAD, HD
ULMER, AJ
机构
[1] FORSCHUNGSINST BORSTEL, DEPT IMMUNOL & CELL BIOL, D-23845 BORSTEL, GERMANY
[2] FORSCHUNGSINST BORSTEL, DEPT IMMUNOCHEM & BIOCHEM MICROBIOL, D-23845 BORSTEL, GERMANY
[3] INDIANA UNIV, SCH MED, NW CTR MED EDUC, GARY, IN 46408 USA
[4] ACAD SCI CZECH REPUBL, INST MOLEC GENET, PRAGUE, CZECH REPUBLIC
[5] OSAKA UNIV, FAC SCI, DEPT CHEM, OSAKA, JAPAN
关键词
D O I
10.1128/IAI.62.11.4709-4715.1994
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We have investigated the interaction of soluble peptidoglycan (sPG), in comparison with lipopolysaccharide (LPS), with human mononuclear cells (MNC) by determining the capacity of sPG to induce interleukin-6 (IL-6) and IL-1 release. In addition, we investigated the modulation of their interaction by anti-CD14 monoclonal antibody and by partial structures of LPS. We found that sPG, like LPS, was able to induce IL-6 and IL-1 production by MNC. However, dose-response experiments revealed that at least 3,000 ng of sPG per mt was necessary for induction, whereas the optimal LPS concentration was 1 ng/ml. Anti-CD14 monoclonal antibody reduced sPG- and LPS-induced IL-6 and IL-1 production. Moreover, partial structures of LPS mere able to reduce monokine production induced by sPG and LPS. We conclude that sPG constitutes, like LPS, an inflammatory cytokine inducer and that CD14 is involved in the activation of human monocytes not only by LPS but also by sPG.
引用
收藏
页码:4709 / 4715
页数:7
相关论文
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