Abstract
We utilized gene targeting by homologous recombination to define the role that MEF, a transcriptional activating member of the ETS family of transcription factors, plays in lymphopoiesis. MEF-/- mice have a profound reduction in the number of NK-T and NK cells. Purified MEF-/- NK cells cannot lyse tumor cell targets and secrete only minimal amounts of IFNgamma. Perforin protein expression is severely impaired in MEF-deficient NK cells, likely accounting for the lack of tumor cell cytotoxicity. Promoter studies and chromatin immunoprecipitation analyses demonstrate that MEF and not ETS-1 directly regulates transcription of the perforin gene in NK cells. Our results uncover a specific role of MEF in the development and function of NK cells and in innate immunity.
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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B-Lymphocytes / immunology
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Cytotoxicity, Immunologic
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DNA-Binding Proteins / deficiency
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DNA-Binding Proteins / genetics
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DNA-Binding Proteins / physiology*
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Gene Expression Regulation
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In Vitro Techniques
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Killer Cells, Natural / immunology*
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Lymphocytes / pathology
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Lymphopoiesis
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Membrane Glycoproteins / genetics*
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Mice
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Mice, Knockout
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Perforin
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Pore Forming Cytotoxic Proteins
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Promoter Regions, Genetic
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T-Lymphocyte Subsets / immunology*
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Transcription Factors / deficiency
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Transcription Factors / genetics
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Transcription Factors / physiology*
Substances
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DNA-Binding Proteins
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Elf4 protein, mouse
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Membrane Glycoproteins
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Pore Forming Cytotoxic Proteins
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Transcription Factors
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Perforin