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首页> 外文期刊>The journal of clinical investigation >MEIS1-mediated transactivation of synaptotagmin-like 1 promotes CXCL12/CXCR4 signaling and leukemogenesis
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MEIS1-mediated transactivation of synaptotagmin-like 1 promotes CXCL12/CXCR4 signaling and leukemogenesis

机译:MEIS1介导的突触素样1的反式激活促进CXCL12 / CXCR4信号传导和白血病发生。

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The TALE-class homeoprotein MEIS1 specifically collaborates with HOXA9 to drive myeloid leukemogenesis. Although MEIS1 alone has only a moderate effect on cell proliferation in vitro, it is essential for the development of HOXA9-induced leukemia in vivo. Here, using murine models of leukemogenesis, we have shown that MEIS1 promotes leukemic cell homing and engraftment in bone marrow and enhances cell-cell interactions and cytokine-mediated cell migration. We analyzed global DNA binding of MEIS1 in leukemic cells as well as gene expression alterations in MEIS1-deficent cells and identified synaptotagmin-like 1 ( Sytl1 , also known as Slp1 ) as the MEIS1 target gene that cooperates with Hoxa9 in leukemogenesis. Replacement of SYTL1 in MEIS1-deficent cells restored both cell migration and engraftment. Further analysis revealed that SYTL1 promotes cell migration via activation of the CXCL12/CXCR4 axis, as SYTL1 determines intracellular trafficking of CXCR4. Together, our results reveal that MEIS1, through induction of SYTL1, promotes leukemogenesis and supports leukemic cell homing and engraftment, facilitating interactions between leukemic cells and bone marrow stroma.
机译:TALE类同源蛋白MEIS1与HOXA9专门协同驱动髓样白血病的发生。尽管仅MEIS1对体外细胞增殖仅具有中等作用,但它对于HOXA9诱导的体内白血病的发展至关重要。在这里,使用白血病发生的小鼠模型,我们已经表明MEIS1促进白血病细胞归巢和骨髓移植,并增强细胞间相互作用和细胞因子介导的细胞迁移。我们分析了白血病细胞中MEIS1的全球DNA结合以及MEIS1缺陷细胞中的基因表达变化,并确定了突触结合素样蛋白1(Sytl1,也称为Slp1)作为与Hoxa9在白血病发生中协同作用的MEIS1目标基因。 MEIS1缺陷细胞中SYTL1的替换恢复了细胞的迁移和植入。进一步的分析表明,SYTL1通过激活CXCL12 / CXCR4轴来促进细胞迁移,因为SYTL1确定了CXCR4的细胞内运输。在一起,我们的结果表明,MEIS1,通过诱导SYTL1,促进白血病的发生并支持白血病细胞的归巢和植入,促进白血病细胞与骨髓基质之间的相互作用。

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