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

Author:

Komine Okiru1,Hayashi Keitaro2,Natsume Waka2,Watanabe Toshio2,Seki Youichi1,Seki Noriyasu1,Yagi Ryoji1,Sukzuki Wataru1,Tamauchi Hidekazu3,Hozumi Katsuto4,Habu Sonoko4,Kubo Masato1,Satake Masanobu2

Affiliation:

1. Research Institute for Biological Sciences, Tokyo University of Science, 2669 Yamazaki, Noda 278-0022, Japan

2. Department of Molecular Immunology, Institute of Development, Aging and Cancer, Tohoku University, Sendai 980-8575, Japan

3. Department of Microbiology plus Parasitology, School of Medicine, Kitasato University, Sagamihara 228-8555, Japan

4. Department of Immunology, Tokai University School of Medicine, Boseidai, Isehara 259-1193, Japan

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.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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