Identification and characterization of thymic epithelial progenitor cells

被引:215
作者
Bennett, AR
Farley, A
Blair, NF
Gordon, J
Sharp, L
Blackburn, CC
机构
[1] Univ Edinburgh, Ctr Genome Res, Edinburgh EH9 3JQ, Midlothian, Scotland
[2] Univ Edinburgh, Inst Cell Anim & Populat Biol, Edinburgh EH9 3JQ, Midlothian, Scotland
[3] Univ Edinburgh, Div Biomed & Clin Lab Sci, Edinburgh EH8 9XD, Midlothian, Scotland
基金
英国惠康基金; 英国医学研究理事会;
关键词
D O I
10.1016/S1074-7613(02)00321-7
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
T cell differentiation and repertoire selection depend critically on several distinct thymic epithelial cell types, whose lineage relationships are unclear. We have investigated these relationships via functional analysis of the epithelial populations within the thymic primordium. Here, we show that mAbs MTS20 and MTS24 identify a population of cells that, when purified and grafted ectopically, can differentiate into all known thymic epithelial cell types, attract lymphoid progenitors, and support CD4(+) and CD8(+) T cell development in nude mice. In contrast, other epithelial populations in the thymic primordium can fulfill none of these functions. These data establish that the MTS20(+)24(+) population is sufficient to generate a functional thymus in vivo and thus argue strongly that all thymic epithelial cell types derive from a common progenitor cell.
引用
收藏
页码:803 / 814
页数:12
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