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The Runx1 Transcription Factor Inhibits the Differentiation of Naive CD4(+) T Cells into the Th2 Lineage by Repressing GATA3 Expression

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 in...

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Detalles Bibliográficos
Autores principales: Komine, Okiru, Hayashi, Keitaro, Natsume, Waka, Watanabe, Toshio, Seki, Youichi, Seki, Noriyasu, Yagi, Ryoji, Sukzuki, Wataru, Tamauchi, Hidekazu, Hozumi, Katsuto, Habu, Sonoko, Kubo, Masato, Satake, Masanobu
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2196077/
https://www.ncbi.nlm.nih.gov/pubmed/12835475
http://dx.doi.org/10.1084/jem.20021200
Descripción
Sumario: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.