A role for Pref-1 and HES-1 in thymocyte development

被引:176
作者
Kaneta, M
Osawa, M
Osawa, M
Sudo, K
Nakauchi, H
Farr, AG
Takahama, Y
机构
[1] Univ Tokushima, Inst Genome Res, Div Expt Immunol, Tokushima 7708503, Japan
[2] Univ Tsukuba, Inst Basic Med Sci, Dept Immunol, Tsukuba, Ibaraki 305, Japan
[3] Kirin Brewery Pharmaceut Res Lab, Gunma, Japan
[4] Japan Sci & Technol Corp, Core Res Evolut Sci & Technol, Tsukuba, Ibaraki, Japan
[5] Univ Washington, Dept Biol Struct, Seattle, WA 98195 USA
[6] Univ Washington, Dept Immunol, Seattle, WA 98195 USA
[7] Japan Sci & Technol Corp, PRESTO, Tokushima, Japan
关键词
D O I
10.4049/jimmunol.164.1.256
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
T lymphocyte development requires a series of interactions between developing thymocytes and thymic epithelial (TE) cells, In this paper we show that TE cells in the developing thymus express Pref-1, a Delta-like cell-surface molecule. In fetal thymus organ cultures (FTOC), thymocyte cellularity was increased by the exogenous dimeric Pref-1 fusion protein, but was reduced by the soluble Pref-1 monomer or anti-Pref-1 Ab, Dimeric Pref-1 in FTOC also increased thymocyte expression of the HES-1 transcription factor. Thymocyte cellularity was increased in FTOC repopulated with immature thymocytes overexpressing HES-1, whereas FTOC from HES-l-deficient mice were hypocellular and unresponsive to the Pref-1 dimer, We detected no effects of either Pref-1 or HES-1 on developmental choice among thymocyte lineages. These results indicate that Pref-1 expressed by TE cells and HES-1 expressed by thymocytes are critically involved in supporting thymocyte cellularity.
引用
收藏
页码:256 / 264
页数:9
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