Abstract
The NFAT family of transcription factors are key regulators of inducible gene expression in the immune system. We examined the function of two NFAT proteins after naïve T helper (T(H)) cell activation. We found that naïve T(H) precursors that are doubly deficient in NFATc2 and NFATc3 intrinsically differentiate into TH(2)-secreting cells, even in the absence of interleukin 4 (IL-4) production. We also found that lack of NFATc2 and NFATc3 obviates the necessity for engagement of CD28 on naïve cells and controls the time required to reach the first cell division upon activation. These results demonstrate a key role for NFATc2 and NFATc3 in modulating T cell receptor responsiveness and regulating subsequent cell division and T(H)2 differentiation.
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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CD28 Antigens / immunology
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Cell Differentiation / drug effects
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Cell Division
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Cell Lineage
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DNA-Binding Proteins / physiology*
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Female
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Interleukin-12 / genetics
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Interleukin-12 / pharmacology
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Interleukin-4 / deficiency
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Interleukin-4 / genetics
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Interleukin-4 / pharmacology
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Lymph Nodes / cytology
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Lymphocyte Activation
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Male
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Mice
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Mice, Inbred BALB C
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Mice, Knockout
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NFATC Transcription Factors
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Nuclear Proteins*
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Receptors, Antigen, T-Cell / immunology*
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Recombinant Proteins / pharmacology
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Specific Pathogen-Free Organisms
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Th2 Cells / cytology*
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Th2 Cells / immunology
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Th2 Cells / metabolism
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Time Factors
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Transcription Factors / physiology*
Substances
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CD28 Antigens
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DNA-Binding Proteins
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NFATC Transcription Factors
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Nfatc2 protein, mouse
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Nfatc3 protein, mouse
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Nuclear Proteins
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Receptors, Antigen, T-Cell
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Recombinant Proteins
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Transcription Factors
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transcription factor NF-AT c3
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Interleukin-12
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Interleukin-4