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首页> 外文期刊>Journal of stem cells. >Characterization of human adipose-derived stem cells cultured in autologous serum after subsequent passaging and long term cryopreservation.
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Characterization of human adipose-derived stem cells cultured in autologous serum after subsequent passaging and long term cryopreservation.

机译:随后传代和长期冷冻保存后,在自体血清中培养的人脂肪干细胞的特征。

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The aim of this study was to evaluate human adipose-derived stem cells (ASCs) from passage 2 (P2) to P8 cultured in medium containing 5% autologous serum (AS) after a long-term cryopreservation with regards to their surface marker expression, differentiation potential, and immunosuppressive effect in vitro. 8-color flow cytometry and real time PCR were used to determine mesenchymal stem cell (MSC) surface marker expression on ASCs from various passages. In vitro differentiation ability and immunomodulatory properties of ASCs were also tested. Flow cytometry showed that all ASCs express typical MSC markers CD29, CD44, CD73, CD90, CD105 simultaneously, but do not express such markers as HLA-DR, CD34, CD14, CD19, and CD45. Furthermore, median fluorescence intensity of positive cell surface markers increased with each subsequent passage indicating the accumulation of protein expression. The multilineage differentiation demonstrated the ability of ASCs from P6 to efficiently differentiate into adipocytes and chondrocytes, but their potential of osteogenic differentiation was diminished. Data from co-culture of ASCs and autologous peripheral blood mononuclear cells (PBMNCs) indicated that ASCs from P3, P6, and P9 significantly reduce the proliferation of PBMNCs at ASCs:PBMNCs ratio 1:1 and this suppression is dose dependent. This study demonstrated that ASCs from P2 to P8, cultured in the presence of AS, represent a highly homogeneous cell population with a peak accumulation of MSC surface proteins at P5 possessing multilineage differentiation ability and significant immunosuppressive properties after double freezing and more than 4 years of cryopreservation.
机译:这项研究的目的是评估经过长期低温保存后在含有5%自体血清(AS)的培养基中培养的第2代(P2)至P8的人类脂肪干细胞(ASC)的表面标志物表达,分化潜能和体外免疫抑制作用。使用8色流式细胞仪和实时PCR来确定来自不同传代的ASC上的间充质干细胞(MSC)表面标记表达。还测试了ASC的体外分化能力和免疫调节特性。流式细胞术表明,所有ASC同时表达典型的MSC标记CD29,CD44,CD73,CD90,CD105,但不表达诸如HLA-DR,CD34,CD14,CD19和CD45的标记。此外,阳性细胞表面标记的中值荧光强度随随后的每次传代而增加,表明蛋白质表达的积累。多谱系分化表明ASCs从P6有效分化为脂肪细胞和软骨细胞的能力,但其成骨分化的潜力却被削弱。来自ASC和自体外周血单个核细胞(PBMNC)共培养的数据表明,来自P3,P6和P9的ASC以1:1的比例将ASCs:PBMNCs的PBMNCs增殖显着降低,并且这种抑制是剂量依赖性的。这项研究表明,在AS存在下培养的从P2到P8的ASC代表了高度均一的细胞群,在P5处具有MSC表面蛋白的峰值积累,具有多系分化能力和双重冷冻后经过4年以上的显着免疫抑制特性。冷冻保存。

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