Prethymic T-cell development defined by the expression of paired immunoglobulin-like receptors

被引:62
作者
Masuda, K
Kubagawa, H
Ikawa, T
Chen, CC
Kakugawa, K
Hattori, M
Kageyama, R
Cooper, MD
Minato, N
Katsura, Y
Kawamoto, H [1 ]
机构
[1] RIKEN Res Ctr Allergy & Immunol, Lab Lymphocyte Dev, Yokohama, Kanagawa 2300045, Japan
[2] Kyoto Univ, Grad Sch Biostudies, Dept Immunol & Cell Biol, Kyoto, Japan
[3] Univ Alabama, Dept Pathol, Div Dev & Clin Immunol, Birmingham, AL 35294 USA
[4] Kyoto Univ, Inst Frontier Med Sci, Dept Immunol, Kyoto, Japan
[5] Kyoto Univ, Inst Virus Res, Lab Growth Regulat, Kyoto 606, Japan
[6] Nihon Univ, Sch Med, Adv Med Res Ctr, Div Cell Regenerat & Transplantat, Tokyo, Japan
关键词
clonal analysis; fetal liver; lineage commitment; T-cell development; thymus;
D O I
10.1038/sj.emboj.7600878
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
T cells are produced in the thymus from progenitors of extrathymic origin. As no specific markers are available, the developmental pathway of progenitors preceding thymic colonization remains unclear. Here we show that progenitors in murine fetal liver and blood, which are capable of giving rise to T cells, NK cells and dendritic cells, but not B cells, can be isolated by their surface expression of paired immunoglobulin-like receptors (PIR). PIR expression is maintained until the earliest intrathymic stage, then downregulated before the onset of CD25 expression. Unlike intrathymic progenitors, generation of prethymic PIR+ progenitors does not require Hes1-mediated Notch signaling. These findings disclose a prethymic stage of T-cell development programmed for immigration of the thymus, which is genetically separable from intrathymic stages.
引用
收藏
页码:4052 / 4060
页数:9
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