9 research outputs found

    Detection of a Functional Hybrid Receptor Îłc/GM-CSFRÎČ in Human Hematopoietic CD34+ Cells

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    A functional hybrid receptor associating the common Îł chain (Îłc) with the granulocyte/macrophage colony-stimulating factor receptor ÎČ (GM-CSFRÎČ) chain is found in mobilized human peripheral blood (MPB) CD34+ hematopoietic progenitors, SCF/Flt3-L primed cord blood (CB) precursors (CBPr CD34+/CD56−), and CD34+ myeloid cell lines, but not in normal natural killer (NK) cells, the cytolytic NK-L cell line or nonhematopoietic cells. We demonstrated, using CD34+ TF1ÎČ cells, which express an interleukin (IL)-15Rα/ÎČ/Îłc receptor, that within the hybrid receptor, the GM-CSFRÎČ chain inhibits the IL-15–triggered Îłc/JAK3-specific signaling controlling TF1ÎČ cell proliferation. However, the Îłc chain is part of a functional GM-CSFR, activating GM-CSF–dependent STAT5 nuclear translocation and the proliferation of TF1ÎČ cells. The hybrid receptor is functional in normal hematopoietic progenitors in which both subunits control STAT5 activation. Finally, the parental TF1 cell line, which lacks the IL-15RÎČ chain, nevertheless expresses both a functional hybrid receptor that controls JAK3 phosphorylation and a novel IL-15α/Îłc/TRAF2 complex that triggers nuclear factor ÎșB activation. The lineage-dependent distribution and function of these receptors suggest that they are involved in hematopoiesis because they modify transduction pathways that play a major role in the differentiation of hematopoietic progenitors

    The role of the extracellular matrix in primary myelofibrosis

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