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FEMS Immunol Med Microbiol ; 45(2): 159-69, 2005 Aug 01.
Article in English | MEDLINE | ID: mdl-16051068

ABSTRACT

We have previously shown that matrix metalloproteinase-9 (MMP-9) activity is greatly enhanced within the active chronic inflammation of Helicobacter pylori infected individuals, of which a major fraction derives from macrophages in the tissue. Here, we have investigated the ability of macrophages to secrete MMPs in response to H. pylori. Human macrophages secrete MMP-9 in response to live and inactivated H. pylori, as well as to specific bacterial products. Protein kinase C, phosphatiolylinositol 3-kinase and calcium uptake channels all play a role in MMP-9 secretion, whereas neither tumour necrosis factor alpha, interleukin-8, nor interleukin-1beta autocrine stimulation appear to contribute. We conclude that human macrophages have the ability to react directly against several H. pylori derived factors, utilising several signalling pathways.


Subject(s)
Helicobacter pylori/immunology , Helicobacter pylori/pathogenicity , Macrophages/enzymology , Macrophages/microbiology , Matrix Metalloproteinase 9/metabolism , Base Sequence , Cytokines/metabolism , Gene Expression , Helicobacter pylori/isolation & purification , Humans , In Vitro Techniques , Macrophage Activation , Macrophages/drug effects , Macrophages/immunology , Matrix Metalloproteinase 9/genetics , Matrix Metalloproteinase 9/immunology , Neutralization Tests , RNA/genetics , Signal Transduction/drug effects , Tissue Inhibitor of Metalloproteinases/immunology , Tissue Inhibitor of Metalloproteinases/metabolism
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