The role of Notch and IL-7 signaling in early thymocyte proliferation and differentiation

被引:76
作者
Balciunaite, G
Ceredig, R
Fehling, HJ
Zúñiga-Pflücker, JC
Rolink, AG
机构
[1] Univ Basel, Dept Clin & Biol Sci DKBW, CH-4058 Basel, Switzerland
[2] Univ Grenoble 1, INSERM, Unit 548, ICH DRDC,CEA G, Grenoble, France
[3] Univ Ulm, Fac Med, Dept Immunol, Ulm, Germany
[4] Univ Toronto, Dept Immunol, Sunnybrook & Womens Coll, Ctr Hlth Sci, Toronto, ON, Canada
关键词
notch; lymphopoiesis; progenitor cells; preTCR; IL-7;
D O I
10.1002/eji.200425822
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We have analyzed the roles of Notch and IL-7 signaling in the proliferation and differentiation of mouse progenitor thymocyte subpopulations cultured on Notch delta-like-1 ligand-expressing OP9 stromal cells. Using bulk and limiting dilution cultures, we show that DN1 and DN2 cells require both Notch and IL-7 signaling for efficient proliferation and differentiation into cytoplasmic TCRP and surface TCR alpha/beta and TCR gamma/delta expressing T cells. Selection for cytoplasmic TCRP-positive cells is dependent on preT alpha expression. Both gamma/delta and alpha/beta TCR expressing T cells arising in culture can be efficiently stimulated by anti-CD3 cross-linking, suggesting that they might be functional. The differentiation of adult, but not fetal, DN1 and DN2 thymocytes into CD4 and/or CD8 expressing cells is inhibited by IL-7. Finally, efficient proliferation and differentiation of DN3 cells requires Notch signaling and preTCR expression, but is independent of IL-7.
引用
收藏
页码:1292 / 1300
页数:9
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