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首页> 外文期刊>Ciência Rural >Isolation and characterization of mesenchymal stem cells derived from bovine Wharton's jelly and their potential for use in cloning by nuclear transfer
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Isolation and characterization of mesenchymal stem cells derived from bovine Wharton's jelly and their potential for use in cloning by nuclear transfer

机译:牛沃顿氏胶冻来源的间充质干细胞的分离,鉴定及其在通过核转移克隆中的应用潜力

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Wharton's jelly is a source of mesenchymal stem cells (MSCs) that had not yet been tested for bovine embryo production by nuclear transfer (NT). Thus, the objective of this study was to isolate, characterize and test MSCs derived from Wharton's jelly for embryo and pregnancy production by NT in cattle. The umbilical cord was collected during calving and cells derived from Wharton's jelly (WJCs) were isolated by explant and cultured in Dulbecco's Modified Eagle Medium. Skin Fibroblasts (FB) were isolated after 6 months of life. Morphological analysis was performed by bright field and scanning electron microscopy (SEM) during cell culture. Phenotypic and genotypic characterization by flow cytometry, immunocytochemistry, RT-PCR and differentiation induction in cell lineages were performed for WJC. In the NT procedure, oocytes at the arrested metaphase II stage were enucleated using micromanipulators, fused with WJCs or FB and later activated artificially. SEM micrographs revealed that WJCs have variable shape under culture. Mesenchymal markers of MSCs (CD29 + , CD73 + , CD90 + and CD105 +) were expressed in bovine-derived WJC cultures, as evidenced by flow cytometry, immunocytochemistry and RT-PCR. When induced, these cells differentiated into osteocytes, chondrocytes and adipocytes. After classification, the WJCs were used in NT. Blastocyst formation rate by NT with WJCs at day 7 was 25.80?±0.03%, similar to blatocyst rate with NT using skin fibroblasts (19.00?±0.07%). Pregnancies were obtained and showed that WJCs constitute a new cell type for use in animal cloning.
机译:沃顿商学院的果冻是间充质干细胞(MSCs)的来源,该细胞尚未通过核移植(NT)进行牛胚生产测试。因此,本研究的目的是分离,鉴定和测试源自沃顿氏果冻的MSC,用于牛NT产生胚胎和产生妊娠。在产犊期间收集脐带,并通过外植体分离出沃顿胶冻(WJCs)衍生的细胞,并在Dulbecco改良的Eagle培养基中培养。六个月的生命后分离出皮肤成纤维细胞(FB)。在细胞培养期间通过明场和扫描电子显微镜(SEM)进行形态分析。 WJC通过流式细胞术,免疫细胞化学,RT-PCR和细胞系分化诱导进行表型和基因型表征。在NT程序中,使用微操纵器摘除处于停滞的II期中期的卵母细胞,将其与WJC或FB融合,然后进行人工激活。 SEM显微照片显示,WJC在培养下具有可变的形状。流式细胞术,免疫细胞化学和RT-PCR证实,MSCs的间充质标记(CD29 +,CD73 +,CD90 +和CD105 +)在牛来源的WJC培养物中表达。当被诱导时,这些细胞分化为骨细胞,软骨细胞和脂肪细胞。分类后,将WJC用于NT。 NT与WJCs在第7天的囊胚形成率是25.80±0.03%,与使用皮肤成纤维细胞的NT的囊胚形成率相似(19.00±0.07%)。获得了怀孕,表明WJC构成了一种用于动物克隆的新细胞类型。

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