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Double labelling of human umbilical cord mesenchymal stem cells with Gd-DTPA and PKH26 and the influence on biological characteristics of hUCMSCs

机译:Gd-DTPA和PKH26双重标记人脐带间充质干细胞及其对hUCMSCs生物学特性的影响

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摘要

The aim of this study was to determine whether double labelling of human umbilical cord mesenchymal stem cells (hUCMSCs) with gadolinium-diethylene triamine penta-acetic acid (Gd-DTPA) and PKH26 influences their biological characteristics. A tissue adherence technique was used to separate and purify the hUCMSCs and flow cytometry was performed to detect the surface markers expressed on them. Gd-DTPA and PKH26 were used to label the stem cells and MRI and fluorescence microscopy were used to detect the double-labelled hUCMSCs. A MTT assay was used to delineate the growth curve. Transmission electron microscopy (TEM) and atomic force microscopy were used to demonstrate the ultrastructural features of the hUCMSCs. Flow cytometry showed that hUCMSCs highly expressed CD29, CD90, CD44 and CD105. No expression of CD31, CD34 and CD45 was detected. Very low expression of HLA-DR and CD40 was detected. Atomic force microscopy showed these cells were long, spindle shaped, and the cytoplasm and nucleus had clear boundaries. After double labelling, TEM showed Gd particles aggregated in the cytoplasm in a cluster pattern. The proliferation activity, cell cycle, apoptosis and differentiation of the stem cells were not influenced by double labelling. Thus a tissue adherence technique is helpful to separate and purify hUCMSCs effectively; and Gd-DTPA and PKH26 are promising tracers in the investigation of migration and distribution of hUCMSCs in vivo.
机译:这项研究的目的是确定用g二乙基三亚乙基五胺五乙酸(Gd-DTPA)和PKH26双重标记人脐带间充质干细胞(hUCMSCs)是否会影响其生物学特性。使用组织粘附技术分离和纯化hUCMSC,并进行流式细胞仪检测其上表达的表面标志物。用Gd-DTPA和PKH26标记干细胞,并用MRI和荧光显微镜检测双标记的hUCMSC。使用MTT测定法描绘生长曲线。透射电子显微镜(TEM)和原子力显微镜用于证明hUCMSCs的超微结构特征。流式细胞仪显示hUCMSCs高表达CD29,CD90,CD44和CD105。没有检测到CD31,CD34和CD45的表达。检测到HLA-DR和CD40的表达非常低。原子力显微镜检查显示这些细胞很长,呈纺锤形,细胞质和细胞核有清晰的边界。双重标记后,TEM显示Gd颗粒以团簇形式聚集在细胞质中。双重标记不影响干细胞的增殖活性,细胞周期,凋亡和分化。因此,组织粘附技术有助于有效地分离和纯化hUCMSC。 Gd-DTPA和PKH26在体内hUCMSC迁移和分布研究中是很有希望的示踪剂。

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