OBJECTIVE:The intracellular signals that contribute to granulocyte colony-stimulating factor (G-CSF) receptor induced stem cell mobilization are poorly characterized. METHODS:We show enhanced G-CSF induced mobilization of stem cells in mice deficient in expression of Src family kinases (SFK-/-), which is associated with hypersensitivity of SFK-/- bone marrow cells to G-CSF as well as sustained activation of signal transducer and activator of transcription-3. RESULTS:A proteome map of the bone marrow fluid derived from wild-type and SFK-/- mice revealed a significant global reduction in the number of proteins in SFK-/- mice compared to controls, which was associated with elevated matrix metalloproteinase-9 levels, reduced stromal-derived factor-1 expression, and enhanced breakdown of vascular cell adhesion molecule-1. Transplantation of wild-type or SFK-/- stem cells into wild-type mice and treatment with G-CSF recapitulated the G-CSF-induced increase in stem cell mobilization noted in SFK-/- nontransplanted mice; however, the increase was significantly less. G-CSF treatment of SFK-/- mice engrafted with wild-type stem cells also demonstrated a modest increase in stem cell mobilization compared to controls, however, the observed increase was greatest in mice completely devoid of SFKs. CONCLUSIONS:These data suggest an involvement of both hematopoietic intrinsic and microenvironmental factors in Src kinase-mediated mobilization of stem cells and identify Src kinases as potential targets for modulating stem cell mobilization.

译文

目的:促成粒细胞集落刺激因子(G-CSF)受体诱导干细胞动员的细胞内信号的特征较差。
方法:我们显示了增强的G-CSF诱导缺乏Src家族激酶(SFK-/-)表达的小鼠干细胞动员,这与SFK-/-骨髓细胞对G-CSF的超敏性以及持续性有关激活信号转导子和转录激活子3。
结果:从野生型和SFK-/-小鼠中提取的骨髓液的蛋白质组图谱显示,与对照组相比,SFK-/-小鼠中蛋白质的数量总体上显着减少,这与基质金属蛋白酶9升高有关水平,减少基质衍生因子1表达,并增强血管细胞粘附分子1的分解。将野生型或SFK-/-干细胞移植到野生型小鼠中并进行G-CSF处理,概括了G-CSF诱导的SFK-/-非移植小鼠中干细胞动员的增加;但是,增加幅度明显较小。对植入野生型干细胞的SFK-/-小鼠进行G-CSF处理,与对照组相比,干细胞动员也有适度的增加,但是,观察到的这种增加在完全没有SFK的小鼠中最大。
结论:这些数据表明造血的内在因素和微环境因素都参与了Src激酶介导的干细胞动员,并确定Src激酶是调节干细胞动员的潜在靶标。

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