首页> 美国卫生研究院文献>Advanced Pharmaceutical Bulletin >The Effect of Mesenchymal Stem Cell-Derived Microvesicles on Erythroid Differentiation of Umbilical Cord Blood-Derived CD34+ Cells
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The Effect of Mesenchymal Stem Cell-Derived Microvesicles on Erythroid Differentiation of Umbilical Cord Blood-Derived CD34+ Cells

机译:间充质干细胞来源的微泡对脐血来源的CD34 +细胞红系分化的影响

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摘要

>Purpose: Mesenchymal stem cells (MSCs) play an important role in the proliferation and differentiation of hematopoietic stem cells (HSCs) in the bone marrow via cell-to-cell contact, as well as secretion of cytokines and microvesicles (MVs). In this study, we investigated the effect of mesenchymal stem cell-derived microvesicles (MSC-MVs) on erythroid differentiation of umbilical cord blood-derived CD34+ cells.>Methods: In this descriptive study, CD34+ cells were cultured with mixture of SCF (10 ng/ml) and rhEPO (5 U/ml) cytokines in complete IMDM medium as positive control group. Then, in MV1- and MV2-groups, microvesicles at 10 and 20 µg/ml concentration were added. After 72 hours, erythroid specific markers (CD71 and CD235a) and genes (HBG1, GATA1, FOG1 and NFE2) were assessed by flow cytometry and qRT-PCR, respectively.>Results: The expression of specific markers of the erythroid lineages (CD71 and GPA) in the presence of different concentration of microvesicles were lower than that of the control group (P<0.001). Also, the expression of specific genes of the erythroid lineages (NFE2, FOG1, GATA1, and HBG1) was investigated in comparison to the internal control (GAPDH). Among all of them, HBG1 and FOG1 genes were significantly decreased to the control group (P<0.0001) but GATA1 and NFE2 gene expressions was not significant.>Conclusion: The results of this study showed that MSC-MVs decrease the erythroid differentiation of umbilical cord blood-derived CD34+ cells. Therefore, MSC-MVs play a key role in the regulation of normal erythropoiesis.
机译:>目的:间充质干细胞(MSC)通过细胞间接触在骨髓中造血干细胞(HSC)的增殖和分化以及细胞因子和细胞因子的分泌中发挥重要作用。微泡(MVs)。在这项研究中,我们研究了间充质干细胞来源的微囊泡(MSC-MVs)对脐血CD34 + 细胞红系分化的影响。>方法:这项描述性研究将CD34 + 细胞与SCF(10 ng / ml)和rhEPO(5 U / ml)细胞因子的混合物一起在完全IMDM培养基中培养,作为阳性对照组。然后,在MV1-和MV2-组中,加入浓度为10和20 µg / ml的微泡。 72小时后,通过流式细胞术和qRT-PCR分别评估了类红细胞特异性标志物(CD71和CD235a)和基因(HBG1,GATA1,FOG1和NFE2)。>结果:存在不同浓度微泡的类红细胞谱系(CD71和GPA)低于对照组(P <0.001)。此外,与内部对照(GAPDH)相比,还研究了类红细胞谱系(NFE2,FOG1,GATA1和HBG1)的特定基因的表达。其中,HBG1和FOG1基因较对照组明显减少(P <0.0001),但GATA1和NFE2基因表达不明显。>结论:研究结果表明,MSC-MVs降低脐带血来源的CD34 + 细胞的红系分化。因此,MSC-MV在正常红细胞生成的调节中起关键作用。

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