Wolfe Margaret, Pochampally Radhika, Swaney William, Reger Roxanne L
Center for Gene Therapy, Tulane University Health Sciences Center, New Orleans, LA, USA.
Methods Mol Biol. 2008;449:3-25. doi: 10.1007/978-1-60327-169-1_1.
We have developed protocols whereby a total of 30-90 x 10(6) hMSCs with an average viability greater than 90% can be produced in a single multilevel Cell Factory from a relatively small (1-3 mL) bone marrow aspirate in 14-20 d. It is possible to generate as many as 5 x 10(8) multipotent stromal cells (MSCs) from a single sample, depending on the number of Cell Factories seeded from the initial isolated hMSCs. Briefly, mononuclear cells are collected from a bone marrow aspirate by density gradient centrifugation. The cells are cultured overnight and the adherent cells are allowed to attach to the flask. Nonadherent cells are removed and the culture expanded for 7-10 d with periodic feeding of the cells. The cells are then harvested and seeded at low density (60-100 cells/cm2) into Nunc Cell Factories. The cells are allowed to expand for an additional 7-10 d, and are then harvested.
我们已经开发出了相关方案,通过该方案,在14至20天内,可从相对少量(1至3毫升)的骨髓抽吸物中,在单个多层细胞工厂中生产出总计30 - 90×10⁶个平均活力大于90%的人间充质干细胞(hMSCs)。根据从最初分离的hMSCs接种的细胞工厂数量,从单个样本中最多可生成5×10⁸个多能间充质干细胞(MSCs)。简而言之,通过密度梯度离心从骨髓抽吸物中收集单核细胞。将细胞培养过夜,使贴壁细胞附着于培养瓶。去除未贴壁细胞,并通过定期给细胞喂食将培养物扩增7至10天。然后收获细胞,并以低密度(60 - 100个细胞/平方厘米)接种到Nunc细胞工厂中。让细胞再扩增7至10天,然后收获。