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- W2165424802 endingPage "2956" @default.
- W2165424802 startingPage "2948" @default.
- W2165424802 abstract "Abstract In this study, the finding that a significant proportion of all dendritic cells (DCs) resident in vivo in the human postnatal thymus displayed a myeloid-related phenotype prompted us to re-examine the developmental origin of thymic DCs, a cell type hitherto considered to represent a homogeneous lymphoid-derived population. We show here that these novel intrathymic DCs are truly myeloid, as they arise from CD34+ early thymic progenitors through CD34lointermediates which have lost the capacity to generate T cells, but display myelomonocytic differentiation potential. We also demonstrate that phenotypically and functionally equivalent myeloid precursors devoid of T-cell potential do exist in vivo in the postnatal thymus. Moreover, although interleukin 7 (IL-7) supports the generation of such myeloid intermediates, we show that their developmental branching from the main intrathymic T-cell pathway is linked to the up-regulation of the myelomonocytic granulocyte macrophage–colony-stimulating factor (GM-CSF) receptor, to the down-regulation of the IL-7 receptor and to the lack of pre–T-cell receptor α (pTα) gene transcriptional activation. Taken together, these data challenge the current view that the thymus is colonized by a lymphoid-restricted progenitor and provide evidence that a more immature precursor population with lymphoid and myelomonocytic potential is actually seeding the human postnatal thymus." @default.
- W2165424802 created "2016-06-24" @default.
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- W2165424802 date "2002-04-15" @default.
- W2165424802 modified "2023-10-01" @default.
- W2165424802 title "Identification of a myeloid intrathymic pathway of dendritic cell development marked by expression of the granulocyte macrophage–colony-stimulating factor receptor" @default.
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- W2165424802 doi "https://doi.org/10.1182/blood.v99.8.2948" @default.
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