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Isolation and purification of rabbit mesenchymal stem cells using an optimized protocol

机译:使用优化方案分离和纯化兔间充质干细胞

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Mesenchymal stem cells were first isolated and grown in vitro by Friedenstein over 40 yr ago; however, their isolation remains challenging as they lack unique markers for identification and are present in very small quantities in mesenchymal tissues and bone marrow. Using whole marrow samples, common methods for mesenchymal stem cell isolation are the adhesion method and density gradient fractionation. The whole marrow sample adhesion method still results in the nonspecific isolation of mononuclear cells, and activation and/or potential loss of target cells. Density gradient fractionation methods are complicated, and may result in contamination with toxic substances that affect cell viability. In the present study, we developed an optimized protocol for the isolation and purification of mesenchymal stem cells based on the principles of hypotonic lysis and natural sedimentation.
机译:间充质干细胞最早是在40年前由Friedenstein分离并体外培养的;然而,它们的分离仍然具有挑战性,因为它们缺乏独特的鉴定标记,并且仅少量存在于间充质组织和骨髓中。使用全骨髓样品,分离间充质干细胞的常用方法是粘附法和密度梯度分级法。整个骨髓样品粘附方法仍然导致单核细胞的非特异性分离,以及靶细胞的活化和/或潜在损失。密度梯度分馏方法很复杂,并可能导致影响细胞生存能力的有毒物质污染。在本研究中,我们基于低渗裂解和自然沉降的原理,开发了分离和纯化间充质干细胞的优化方案。

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