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首页> 外文期刊>American journal of clinical and experimental immunology >A protocol for isolation and culture of mesenchymal stem cells from human gingival tissue
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A protocol for isolation and culture of mesenchymal stem cells from human gingival tissue

机译:来自人牙龈组织的间充质干细胞分离和培养的方案

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Human gingiva-derived mesenchymal stem cells (GMSCs) have been considered to be a better source of MSCs for cell therapy in some immunological diseases. We describe a protocol for isolation and culture of mesenchymal stem cells (MSCs) from human gingival tissue in detail, which provides a methodology to help clinical researches and clinical trial. GMSCs are generally isolated from a remnant or discarded tissue following a routine dental procedure, then cultured in complete culture medium at 37°C in a humidified tissue culture incubator with 5% CO 2 and 95% O 2 . Non-adherent cells are removed after 48~72 h and the fresh medium is replaced. When primary cultures become 80%~90% confluent, the plastic-adherent cells are treated with 0.25% trypsin-EDTA and subcultured. A purified population of GMSCs can be obtained 2-3 weeks after the initiation of culture.
机译:人牙龈衍生的间充质干细胞(GMSCs)被认为是一些免疫疾病中细胞疗法的MSCs的更好来源。 我们详细描述了一种用于从人牙龈组织中分离和培养间充质干细胞(MSCs)的方案,这提供了有助于有助于临床研究和临床试验的方法。 在常规牙科手术后,GMSCs通常与残留或丢弃的组织分离,然后在37℃下在具有5%CO 2和95%O 2的加湿组织培养箱中在37℃下在完全培养基中培养。 在48〜72小时后除去非粘附细胞,并更换新鲜培养基。 当原发性培养物变为80%〜90%汇合时,用0.25%胰蛋白酶-EDTA和转培喂,塑性粘附细胞处理。 在发起培养后2-3周可以获得纯化的GMSC群。

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