Regulation of γδ versus αβ T lymphocyte differentiation by the transcription factor SOX13

被引:138
作者
Melichar, Heather J.
Narayan, Kavitha
Der, Sandy D.
Hiraoka, Yoshiki
Gardiol, Noemie
Jeannet, Gregoire
Held, Werner
Chambers, Cynthia A.
Kang, Joonsoo
机构
[1] Univ Massachusetts, Sch Med, Dept Pathol, Grad Program Immunol & Virol, Worcester, MA 01655 USA
[2] Univ Toronto, Dept Lab Med & Pathobiol, Program Proteom & Bioinformat, Toronto, ON, Canada
[3] Keio Univ, Sch Med, Dept Anat, Shinjuku Ku, Tokyo 1608582, Japan
[4] Ludwig Inst Canc Res, Lausanne Branch, CH-1066 Epalinges, Switzerland
[5] Univ Lausanne, CH-1066 Epalinges, Switzerland
关键词
D O I
10.1126/science.1135344
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
alpha beta and gamma delta 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 gamma delta-specific gene in the immune system. Using Sox13 transgenic mice, we showed that this transcription factor promotes gd T cell development while opposing ab T cell differentiation. Conversely, mice deficient in Sox13 expression exhibited impaired development of gd T cells but not ab 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.
引用
收藏
页码:230 / 233
页数:4
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