Role of virulence factors, cell components and adhesion in Helicobacter pylori-mediated iNOS induction in murine macrophages

被引:9
作者
Assmann, IA
Enders, GA
Püls, J
Rieder, G
Haas, R
Hatz, RA
机构
[1] Univ Munich, Klinikum Grosshadern, Dept Surg, D-81377 Munich, Germany
[2] Univ Munich, Klinikum Grosshadern, Inst Surg Res, D-81377 Munich, Germany
[3] Univ Munich, Max Von Petterkofer Inst Hyg & Med Microbiol, D-81377 Munich, Germany
[4] Howard Hughes Res Inst, Ann Arbor, MI USA
来源
FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY | 2001年 / 30卷 / 02期
关键词
Helicobacter pylori; inducible nitric oxide synthase; murine macrophage; adhesion;
D O I
10.1111/j.1574-695X.2001.tb01561.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
To investigate the mechanisms involved in Helicobacter pylori-mediated inducible nitric oxide synthase (iNOS) upregulation in mononuclear cells we cocultivated human THP-I acute monocytic leukemia cells and murine J774A.1 professional macrophages with different H. pylori wild-type strains and mutants. We have shown that H. pylori-mediated iNOS induction in J774A.1 is independent of established virulence factors but dependent on direct interaction between bacteria and cells. In J774A.1, iNOS was equally upregulated by the wild-type strains J99, 26695, P12. and P1 as well as by mutants lacking the cag pathogenicity island, vacA, katA, alpAB genes and the hp0043 gene taking part in lipopolysaccharide biosynthesis when direct cell contact was allowed but not when bacteria and cells were separated by protein-permeable filter membranes. In contrast, iNOS was not induced in THP-I. This indicates that H. pylori-mediated iNOS induction in J774A.1 is independent of important virulence factors whereas cell contact is crucial which suggests a role of adhesion or phagocytosis. (C) 2001 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:133 / 138
页数:6
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