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首页> 外文期刊>Journal of Cell Communication and Signaling >K562 chronic myeloid leukemia cells modify osteogenic differentiation and gene expression of bone marrow stromal cells
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K562 chronic myeloid leukemia cells modify osteogenic differentiation and gene expression of bone marrow stromal cells

机译:K562慢性粒细胞白血病细胞改变骨髓基质细胞的成骨分化和基因表达

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Bone marrow (BM) microenvironment plays an important role in normal and malignant hematopoiesis. As a consequence of interaction with the leukemic cells, the stromal cells of the bone marrow become deregulated in their normal function and gene expression. In our study, we found that mesenchymal stem cells (MSC) from BM of chronic myeloid leukemia (CML) patients have defective osteogenic differentiation and on interaction with K562 CML cells, the normal MSC showed reduced osteogenic differentiation. On interaction with K562 cells or its secreted factors, MSC acquired phenotypic abnormalities and secreted high levels of IL6 through NF?oB activation. The MSC derived secreted factors provided a survival advantage to CML cells from imatinib induced apoptosis. Thus, a therapy targeting stromal cells in addition to leukemia cells might be more effective in eliminating CML cells.
机译:骨髓(BM)微环境在正常和恶性造血过程中起着重要作用。与白血病细胞相互作用的结果是,骨髓基质细胞在其正常功能和基因表达中变得失调。在我们的研究中,我们发现来自慢性髓性白血病(CML)患者的BM的间充质干细胞(MSC)具有成骨分化不良,并且在与K562 CML细胞相互作用时,正常MSC显示出成骨分化降低。与K562细胞或其分泌因子相互作用后,MSC获得了表型异常,并通过NF?oB激活分泌了高水平的IL6。 MSC衍生的分泌因子为伊马替尼诱导的细胞凋亡为CML细胞提供了生存优势。因此,除白血病细胞外,针对基质细胞的疗法在消除CML细胞方面可能更有效。

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