Notch signaling controls the generation and differentiation of early T lineage progenitors

被引:299
作者
Sambandam, A
Maillard, I
Zediak, VP
Xu, LW
Gerstein, RM
Aster, JC
Pear, WS
Bhandoola, A [1 ]
机构
[1] Univ Penn, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
[2] Univ Penn, Div Hematol Oncol, Philadelphia, PA 19104 USA
[3] Univ Penn, Abramson Family Canc Res Inst, Philadelphia, PA 19104 USA
[4] Univ Penn, Inst Med Engn, Philadelphia, PA 19104 USA
[5] Univ Massachusetts, Sch Med, Dept Mol Genet & Microbiol, Worcester, MA 01655 USA
[6] Harvard Univ, Sch Med, Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
关键词
D O I
10.1038/ni1216
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Signaling by the transmembrane receptor Notch is critical for T lineage development, but progenitor subsets that first receive Notch signals have not been defined. Here we identify an immature subset of early T lineage progenitors (ETPs) in the thymus that expressed the tyrosine kinase receptor Flt3 and had preserved B lineage potential at low progenitor frequency. Notch signaling was active in ETPs and was required for generation of the ETP population. Additionally, Notch signals contributed to the subsequent differentiation of ETPs. In contrast, multipotent hematopoietic progenitors circulated in the blood even in the absence of Notch signaling, suggesting that critical Notch signals during early T lineage development are delivered early after thymic entry.
引用
收藏
页码:663 / 670
页数:8
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