Regulation of γδ Versus αß T Lymphocyte Differentiation by the Transcription Factor SOX13

Author:

Melichar Heather J.1234,Narayan Kavitha1234,Der Sandy D.1234,Hiraoka Yoshiki1234,Gardiol Noemie1234,Jeannet Gregoire1234,Held Werner1234,Chambers Cynthia A.1234,Kang Joonsoo1234

Affiliation:

1. Department of Pathology, Graduate Program in Immunology and Virology, University of Massachusetts Medical School, 55 Lake Avenue North, Worcester, MA 01655, USA.

2. Department of Laboratory Medicine and Pathobiology, Program in Proteomics and Bioinformatics, University of Toronto, Toronto, Canada.

3. Department of Anatomy, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan.

4. Ludwig Institute for Cancer Research, Lausanne Branch and University of Lausanne, Chemin Des Boveresses 155, 1066 Epalinges, Switzerland.

Abstract

αβ and γδ T cells originate from a common, multipotential precursor population in the thymus, but the molecular mechanisms regulating this lineage-fate decision are unknown. We have identified Sox13 as a γδ-specific gene in the immune system. Using Sox13 transgenic mice, we showed that this transcription factor promotes γδ T cell development while opposing αβ T cell differentiation. Conversely, mice deficient in Sox13 expression exhibited impaired development of γδ T cells but not αβ T cells. One mechanism of SOX13 function is the inhibition of signaling by the developmentally important Wnt/T cell factor (TCF) pathway. Our data thus reveal a dominant pathway regulating the developmental fate of these two lineages of T lymphocytes.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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