Abstract
Differentiation of naive CD4+ T cells into helper T (Th) cells is controlled by a combination of several transcriptional factors. In this study, we examined the functional role of the Runx1 transcription factor in Th cell differentiation. Naive T cells from transgenic mice expressing a dominant interfering form of Runx1 exhibited enhanced interleukin 4 production and efficient Th2 differentiation. In contrast, transduction of Runx1 into wild-type T cells caused a complete attenuation of Th2 differentiation and was accompanied by the cessation of GATA3 expression. Furthermore, endogenous expression of Runx1 in naive T cells declined after T cell receptor stimulation, at the same time that expression of GATA3 increased. We conclude that Runx1 plays a novel role as a negative regulator of GATA3 expression, thereby inhibiting the Th2 cell differentiation.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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CD4-Positive T-Lymphocytes / physiology*
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Cell Differentiation
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Cell Lineage*
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Cells, Cultured
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Core Binding Factor Alpha 2 Subunit
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DNA-Binding Proteins / genetics*
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DNA-Binding Proteins / physiology*
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GATA3 Transcription Factor
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Interleukin-4 / genetics
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Mice
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Mice, Inbred BALB C
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Mice, Inbred C57BL
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Proto-Oncogene Proteins*
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Receptors, Antigen, T-Cell / physiology
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Receptors, Interleukin-4 / physiology
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Repressor Proteins / physiology*
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Th2 Cells / physiology*
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Trans-Activators / genetics*
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Transcription Factors / physiology*
Substances
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Core Binding Factor Alpha 2 Subunit
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DNA-Binding Proteins
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GATA3 Transcription Factor
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Gata3 protein, mouse
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Proto-Oncogene Proteins
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Receptors, Antigen, T-Cell
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Receptors, Interleukin-4
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Repressor Proteins
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Runx1 protein, mouse
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Trans-Activators
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Transcription Factors
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Interleukin-4