International Center for Biotechnology, Osaka University, 2-1, Yamada-oka, Suita, Osaka, 565-0871, Japan,
Cytotechnology. 2003 Nov;43(1-3):89-96. doi: 10.1023/b:cyto.0000039911.46200.61.
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 \times 10(5) nucleated cells/cm(2)) with DMEM medium containing 10% serum (FCS or donor serum) and basic fibroblast growth factor, and incubated at 37 degrees C under a 5% CO(2) 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.
开发了一种不使用胎牛血清 (FCS) 的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。不使用密度梯度离心,将骨髓抽吸物倒入含有 DMEM 培养基(含 10%血清(FCS 或供体血清)和碱性成纤维细胞生长因子)的培养皿中(6.0×10(5)个核细胞/cm(2)),并在 37 度下孵育。在 5% CO(2) 气氛中。用含有人血清和碱性成纤维细胞生长因子(10ng/ml)的培养基孵育的贴壁细胞的密度在 19 天几乎达到汇合,是仅含 FCS 的培养基中的 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 的培养基中的 0.1-0.6 倍。在含有人血清和碱性成纤维细胞生长因子的培养基中孵育 19 天后收获的细胞中 CD45(-) CD105(+) 细胞的含量高于 90%。即使在进一步传代至 17 个群体倍增水平的培养基中培养,这种高含量和软骨形成活性(通过微球培养和番红 O 染色证实)仍得以维持。因此,该方法可能适用于软骨再生的 MSC 体外扩增。