Martelli Fabrizio, Ghinassi Barbara, Lorenzini Rodolfo, Vannucchi Alessandro M, Rana Rosa Alba, Nishikawa Mitsuo, Partamian Sandra, Migliaccio Giovanni, Migliaccio Anna Rita
Hematology, Oncology and Molecular Medicine, Istituto Superiore Sanità, Rome, Italy.
Stem Cells. 2008 Apr;26(4):912-9. doi: 10.1634/stemcells.2007-0777. Epub 2008 Feb 14.
We have recently shown that Mpl, the thrombopoietin receptor, is expressed on murine mast cells and on their precursors and that targeted deletion of the Mpl gene increases mast cell differentiation in mice. Here we report that treatment of mice with thrombopoietin or addition of this growth factor to bone marrow-derived mast cell cultures severely hampers the generation of mature cells from their precursors by inducing apoptosis. Analysis of the expression profiling of mast cells obtained in the presence of thrombopoietin suggests that thrombopoietin induces apoptosis of mast cells by reducing expression of the transcription factor Mitf and its target antiapoptotic gene Bcl2.
我们最近发现,血小板生成素受体Mpl在小鼠肥大细胞及其前体上表达,并且Mpl基因的靶向缺失会增加小鼠肥大细胞的分化。在此我们报告,用血小板生成素处理小鼠或向骨髓来源的肥大细胞培养物中添加这种生长因子,会通过诱导凋亡严重阻碍其前体产生成熟细胞。对在血小板生成素存在下获得的肥大细胞表达谱分析表明,血小板生成素通过降低转录因子Mitf及其靶标抗凋亡基因Bcl2的表达来诱导肥大细胞凋亡。