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

نویسندگان

  • Okiru Komine
  • Keitaro Hayashi
  • Waka Natsume
  • Toshio Watanabe
  • Youichi Seki
  • Noriyasu Seki
  • Ryoji Yagi
  • Wataru Sukzuki
  • Hidekazu Tamauchi
  • Katsuto Hozumi
  • Sonoko Habu
  • Masato Kubo
  • Masanobu Satake
چکیده

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.

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عنوان ژورنال:
  • The Journal of Experimental Medicine

دوره 198  شماره 

صفحات  -

تاریخ انتشار 2003