首页> 外文期刊>Transplantation Proceedings >Correlation between the immature characteristics of umbilical cord blood-derived mesenchymal stem cells and engraftment of hematopoietic stem cells in NOD/SCID mice.
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Correlation between the immature characteristics of umbilical cord blood-derived mesenchymal stem cells and engraftment of hematopoietic stem cells in NOD/SCID mice.

机译:NOD / SCID小鼠脐带血间充质干细胞未成熟特性与造血干细胞植入之间的相关性。

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Umbilical cord blood (UCB)-derived mesenchymal stem cells (MSC) facilitate the engraftment of human (h) hematopoietic stem cells when transplanted simultaneously in animal and human studies. However, the type of MSCs that preferentially enhance the engraftment of HSCs is unknown. Recent studies have shown that MSCs derived from a single source are heterogeneous in terms of cell size, morphology, proliferation rate, and differentiation potential. This study was designed to investigate the properties of UCB-MSCs, which influence the engraftment of hHSCs in a NOD/SCID mouse model. We categorized MSCs as being the most effective (UCB-352 MSCs) or the least effective (UCB-156 MSCs) at promoting the homing and engraftment of HSCs, and compared the characteristics of these 2 MSC populations. We observed that the 2 populations showed differences in characteristics typical of immature MSCs, and related to proliferation potential. We showed that UCB-352 MSCs, which proliferate quickly, preferentially enhanced the engraftment of HSCs in NOD/SCID mice. In addition, we observed differences in the pattern of both PODXL and Oct4 expression, and in the levels of cytokines such as SDF-1 and SCF using flow cytometry and membrane arrays. The more effective UCB-352 MSCs expressed higher levels of PODXL and Oct4, which were associated with immaturity, than did the UCB-156 MSCs. Furthermore, UCB-352 cells secreted greater levels of SDF-1 and SCF, both of which are required for hematopoiesis. We propose that the proliferation potential of UCB-MSCs, coupled with their immature characteristics, may serve as a novel standard to promote the homing and engraftment of HSCs.
机译:当在动物和人类研究中同时移植时,脐带血(UCB)来源的间充质干细胞(MSC)有助于人类(h)造血干细胞的移植。然而,尚不清楚优先增强HSCs植入的MSC类型。最近的研究表明,从单一来源衍生的MSC在细胞大小,形态,增殖速率和分化潜能方面是异质的。这项研究旨在调查UCB-MSC的特性,这些特性会影响hHSC在NOD / SCID小鼠模型中的植入。我们将MSC归类为促进HSC归巢和植入的最有效(UCB-352 MSC)或最不有效(UCB-156 MSC),并比较了这两个MSC群体的特征。我们观察到,这两个种群在不成熟的MSC的典型特征上存在差异,并且与增殖潜能有关。我们显示,UCB-352 MSC增殖迅速,优先增强了NOC / SCID小鼠中HSC的植入。此外,我们使用流式细胞仪和膜阵列观察到PODXL和Oct4表达模式的差异,以及SDF-1和SCF等细胞因子的水平。与UCB-156 MSC相比,更有效的UCB-352 MSC表达更高水平的PODXL和Oct4,这与不成熟有关。此外,UCB-352细胞分泌更高水平的SDF-1和SCF,这两者都是造血作用所必需的。我们建议,UCB-MSCs的增殖潜能及其不成熟的特征,可以作为促进HSCs归巢和移植的新标准。

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