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Expression of CD146 and Regenerative Cytokines by Human Placenta-Derived Mesenchymal Stromal Cells upon Expansion in Different GMP-Compliant Media

机译:人胎盘衍生的间充质细胞在不同GMP标准介质中膨胀后的CD146和再生细胞因子的表达

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Mesenchymal stromal cells (MSCs) have been successfully employed in clinical applications. In most studies, autologous MSCs from the bone marrow (bmMSCs) were used, and others employed autologous adipose tissue-derived stromal cells (ADSCs). Recently, clinical feasibility studies provided evidence that MSCs from human term placenta (pMSCs) can be used for homologous therapy facilitating access to regenerative cells in emergency situations, when autologous cells are not available or not suitable. We therefore investigated the expression of MSC stemness marker CD146 and the expression of neuro- and myoregenerative cytokines by human pMSCs after expansion in three different media compliant with good manufacturing protocols (GMP) in comparison to pMSCs expanded in a commercial MSC expansion media. To replace xenobiotic serum in the GMP-compliant media employed in this study, either human serum, human serum plus platelet lysate (PLL), or human plasma plus PLL was used. We report that enrichment of media with PLL accelerates pMSC proliferation but reduces the expression of the stemness marker CD146 significantly, while PLL deprivation enhanced the CD146 expression. In contrast, the reduced expression of CD146 by PLL deprivation was not observed on bmMSCs. The expression of the cytokines investigated was not modulated significantly by PLL. We conclude that accelerated expansion of pMSCs in GMP-compliant media enriched by PLL reduces the expression of stemness marker CD146, but does not influence the expression of neuro- and myoregenerative cytokines.
机译:在临床应用中已成功使用间充质基质细胞(MSCs)。在大多数研究中,使用来自骨髓(BMMSCs)的自体MSC,其他物质采用自体脂肪组织衍生的基质细胞(ADSC)。最近,临床可行性研究提供了胎盘(PMSCs)的MSCs可用于促进在急诊情况下促进进入再生细胞的同源治疗,当时自体细胞或不适合。因此,我们研究了MSC茎标志物CD146的表达,并在符合商业MSC膨胀介质中扩增的PMSCS扩增了良好的制造方案(GMP)后,人PMSCs在膨胀后,人PMSC的表达和神经和肌瘤细胞因子的表达。为了替换本研究中使用的GMP兼容介质中的Xenobiotic血清,使用人血清,人血清加血小板裂解物(PLL)或人血浆加pLL。我们报告称PLL的富集培养基加速PMSC增殖,但显着降低了茎秆标记CD146的表达,而PLL剥夺增强了CD146表达。相反,在BMMSC上未观察到通过PLL剥夺的CD146表达降低。研究的细胞因子的表达未通过PLL显着调节。我们得出结论,通过PLL富集的GMP标准培养基加速了PMSCs的扩增减少了茎秆标志物CD146的表达,但不会影响神经和肌瘤细胞因子的表达。

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