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Ex vivo expansion of hematopoietic stem cells derived from umbilical cord blood in rotating wall vessel

机译:脐带血在旋转壁血管中的离体造血干细胞的体外扩增

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Expansion of umbilical cord blood mononuclear cells (UCB MNCs) was carried out in a rotating wall vessel (RWV) bioreactor and tissue culture flasks (T-flasks) in serum-containing medium supplemented with relatively low doses of purified recombinant human cytokines (5.33 ng/ml IL-3, 16 ng/ml SCF, 3.33 ng/ml G-CSF, 2.13 ng/ml GM-CSF, 7.47 ng/ml FL and 7.47 ng/ml TPO) for 8 days. The cell density, pH and osmolality of the culture medium in the two culture systems were measured every 24h. Flow cytometric assay for CD34+ cells was carried out at 0, 144 and 197 h and methylcellulose colony assays were performed at 0, 72, 144 and 197 h. The pH and osmolality of the medium in the two culture systems were maintained in the proper ranges for hematopoietic stem cells (HSCs) and progenitors culture. The RWV bioreactor, combined with a cell-dilution feeding protocol, was efficient to expand UCB MNCs. At the end of 200 h culture, the total cell number was multiplied by 435.5+/-87.6 times, and CD34+ cells 32.7+/-15.6 times, and colony-forming units of granulocyte-macrophage (CFU-GM) 21.7+/-4.9 times. While in T-flasks, however, total cells density changed mildly, CD34+ cells and CFU-GM decreased in number. It is demonstrated that the RWV bioreactor can provide a better environment for UCB MNCs expansion, enhance the contact between HSCs and accessory cells and make the utilization of cytokines more effective than T-flask.
机译:在旋转壁容器(RWV)生物反应器和组织培养瓶(T瓶)中,在含血清的培养基中扩增脐带血单核细胞(UCB MNC),该培养基中添加了相对低剂量的纯化重组人细胞因子(5.33 ng / ml IL-3、16 ng / ml SCF,3.33 ng / ml GM-CSF,2.13 ng / ml GM-CSF,7.47 ng / ml FL和7.47 ng / ml TPO),共8天。每24小时测量两个培养系统中培养基的细胞密度,pH和重量摩尔渗透压浓度。 CD34 +细胞的流式细胞术分析在0、144和197 h进行,甲基纤维素菌落分析在0、72、144和197 h进行。对于造血干细胞(HSC)和祖细胞培养,两种培养系统中培养基的pH和重量摩尔渗透压浓度均保持在适当的范围内。 RWV生物反应器与细胞稀释饲喂方案相结合,可以有效地扩展UCB MNC。在200 h培养结束时,总细胞数乘以435.5 +/- 87.6倍,CD34 +细胞乘以32.7 +/- 15.6倍,粒细胞巨噬细胞(CFU-GM)的菌落形成单位乘以21.7 +/- 4.9倍然而,在T瓶中,总细胞密度变化不大,CD34 +细胞和CFU-GM的数量减少。事实证明,RWV生物反应器可以为UCB MNCs的扩增提供更好的环境,增强HSC与辅助细胞之间的接触,并使细胞因子的利用比T烧瓶更有效。

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