Isolation of the most immature population of murine fetal thymocytes that includes progenitors capable of generating T, B, and myeloid cells

被引:49
作者
Hattori, N [1 ]
Kawamoto, H [1 ]
Katsura, Y [1 ]
机构
[1] KYOTO UNIV,CHEST DIS RES INST,DEPT IMMUNOL,KYOTO 60601,JAPAN
关键词
D O I
10.1084/jem.184.5.1901
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Thymus cells of murine fetuses at day 12 of gestation are exclusively of the CD3(-)CD4(-)CD8(-)CD44(+)CD25(-) phenotype, which is known as a hallmark of the most immature subset of thymus cells. In the present study, we show that day 12 fetal thymus (FT) cells express Fc gamma RII/ III (FcR) at a broad range of levels on their surface. The FcR(+) FT cells seem to represent T lineage cells, because a large majority of them express the T Lineage specific transcription factors TCF-1 and GATA-3 as well as CD3 epsilon in the cytoplasm. Also shown is that the FcR(-) population contains progenitors capable of developing into not only T cells but also B and myeloid cells, whereas FcR(+) progenitors are mostly committed to the T lineage. These findings indicate that thymic T lineage cells express FcR on their surface at the earliest stage of differentiation, and thus FcR is a useful marker in isolating the most immature population of murine FT cells.
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页码:1901 / 1908
页数:8
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