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In vitro Proliferation of Human Bone Marrow Mesenchymal Stem Cells Employing Donor Serum and Basic Fibroblast Growth Factor

机译:利用供体血清和碱性成纤维细胞生长因子的人骨髓间充质干细胞的体外增殖

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摘要

A method for the in vitro proliferation of human bone marrow mesenchymal stem cells (MSCs) employing a medium not containing fetal calf serum (FCS) was developed for a regenerative medicine of cartilage using MSCs. Without using density-gradient centrifugation, the bone marrow aspirate was poured into a dish (6.0 imes 105 nucleated cells/cm2) with DMEM medium containing 10% serum (FCS or donor serum) and basic fibroblast growth factor, and incubated at 37 °C under a 5% CO2 atmosphere. The density of adhesive cells incubated with the medium containing human serum and basic fibroblast growth factor (10 ng/ml) almost reached confluence at 19d and was 1.4-2.7 times that in the medium containing only FCS. The density of cells incubated with the medium containing only human serum was 0.1-0.6 times that in the medium containing only FCS. The content of CD45- CD105+ cells among the cells harvested after a 19-d incubation in the medium containing human serum and basic fibroblast growth factor was higher than 90%. This high content and chondrogenic activity, which was confirmed by pellet cultivation and staining with Safranine O, were maintained even after further subcultivation in the medium to 17 population doubling levels. Consequently, this method might be applicable to in vitro proliferation of MSCs for the regeneration of cartilage.
机译:开发了一种使用不含胎牛血清(FCS)的培养基体外扩增人骨髓间充质干细胞(MSCs)的方法,用于使用MSCs进行软骨再生医学。在不使用密度梯度离心的情况下,将骨髓穿刺液倒入含有10%血清(10%的DMEM培养基)的培养皿中(6.0乘以10 5 有核细胞/ cm 2 )。 FCS或供体血清)和碱性成纤维细胞生长因子,并在5%CO2气氛下于37°C孵育。与含有人血清和碱性成纤维细胞生长因子(10 ng / ml)的培养基一起孵育的黏附细胞的密度在19天时几乎达到汇合,是仅含有FCS的培养基的1.4-2.7倍。用仅含人血清的培养基孵育的细胞密度是仅含FCS的培养基的0.1-0.6倍。在含人血清和碱性成纤维细胞生长因子的培养基中培养19天后,收获的细胞中CD45 - CD105 + 细胞的含量高于90%。这种高含量和成软骨活性,通过沉淀培养和用番红O染色得到证实,甚至在中度培养至17倍的种群倍增水平之后也得以保持。因此,该方法可能适用于MSCs的体外增殖以用于软骨的再生。

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