作者: H.R. Rodewald , K. Kretzschmar , S. Takeda , C. Hohl , M. Dessing
DOI: 10.1002/J.1460-2075.1994.TB06743.X
关键词: Molecular biology 、 Immunology 、 Thymocyte 、 Population 、 Haematopoiesis 、 Myeloid 、 Gene rearrangement 、 CD8 、 T cell 、 Biology 、 CD3
摘要: Phenotype and commitment of thymus-colonizing precursors are unknown. Here we report the identification T lineage-committed (designated prothymocytes) in murine fetal blood at day 15.5 development. Fetal pro-thymocytes Thy-1+c-kit(low)CD3- contrast to blood-derived pluripotent hematopoietic progenitors which Thy-1-c-kit+. Upon transfer into thymus, generate a single wave CD4+CD8+ thymocytes subsequently mature TCR alpha beta+ peripheral cells. However, lack multipotent progenitor potential since they fail reconstitute B lymphocytes myeloid erythroid lineages. In contrast, as well lineages reconstituted from progenitors. Pro-thymocytes equally present athymic mice, suggesting that this novel precursor population is prior thymus colonization represents earliest lineage identified.