Abstract
We have previously identified the STK receptor tyrosine kinase as a key regulator of macrophage activation and cell-mediated immune responses. Here we demonstrate that, although MSP activation of STK inhibits NO production by macrophages in response to heat-killed Listeria monocytogenes, STK-deficient mice exhibit increased susceptibility to infection with Listeria.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Animals
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Cells, Cultured
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Disease Susceptibility
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Growth Substances / pharmacology
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Hepatocyte Growth Factor*
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Interferon-gamma / pharmacology
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Listeria monocytogenes / metabolism
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Listeria monocytogenes / pathogenicity
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Listeriosis / enzymology*
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Listeriosis / microbiology
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Liver / microbiology
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Macrophages, Peritoneal / cytology
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Macrophages, Peritoneal / drug effects
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Mice
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Mice, Knockout
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Nitric Oxide / biosynthesis
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Proto-Oncogene Proteins*
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Receptor Protein-Tyrosine Kinases / genetics
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Receptor Protein-Tyrosine Kinases / metabolism
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Receptor Protein-Tyrosine Kinases / physiology*
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Receptors, Cell Surface / genetics
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Receptors, Cell Surface / metabolism
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Receptors, Cell Surface / physiology*
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Spleen / microbiology
Substances
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Growth Substances
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Proto-Oncogene Proteins
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Receptors, Cell Surface
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macrophage stimulating protein
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Nitric Oxide
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Hepatocyte Growth Factor
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Interferon-gamma
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RON protein
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Receptor Protein-Tyrosine Kinases