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Clumping and Viability of Bone Marrow Derived Mesenchymal Stromal Cells under Different Preparation Procedures: A Flow Cytometry-Based In Vitro Study

机译:不同制剂手术下骨髓衍生间充质基质细胞的块和活力:流式细胞术基体外研究

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Complications of microocclusions have been reported after intra-arterial delivery of mesenchymal stromal cells. Hence, quantification and efficient limitation of cell clumps in suspension before transplantation is important to reduce the risk. We used a flow cytometry-based pulse-width assay to assess the effects of different cell suspension concentrations (0.2-2.0 x 10(6)/mL), storage solutions (complete growth medium, Dulbecco's phosphate-buffered saline, and normal saline), storage time in suspension (0-9 h), and freeze-thawing procedure on the clumping of rat bone marrow derived mesenchymal stromal cells (BMMSCs) and also evaluated cell viability at the same time. Surprisingly, increasing the cell concentration did not result in more cell clumps in vitro. Freshly harvested (fresh) cells in normal saline had significantly fewer cell clumps and also displayed high viability (>90%). A time-dependent reduction in viability was observed for cells in all three storage solutions, without any significant change in the clumping tendency except for cells in medium. Fresh cells were more viable than their frozen-thawed counterparts, and fresh cells in normal saline had fewer cell clumps. In conclusion, cell clumping and viability could be affected by different cell preparation procedures, and quantification of cell clumping can be conducted using the flow cytometry-based pulse-width assay before intra-arterial cell delivery.
机译:在间充质基质细胞的动脉内递送后,已经报道了微皮的并发症。因此,移植前悬浮液中细胞团块的量化和有效限制对于降低风险是重要的。我们使用了流式细胞术的脉冲宽度测定,以评估不同细胞悬浮浓度的影响(0.2-2.0×10(6)/ ml),储存溶液(完全生长培养基,Dulbecco磷酸盐缓冲盐水和生理盐水) ,悬浮液中的储存时间(0-9小时),并在大鼠骨髓衍生的间充质基质细胞(BMMSCs)簇中的冻融程序,并同时评估细胞活力。令人惊讶的是,增加细胞浓度不会导致体外更多的细胞团块。正常盐水中的新鲜收获(新鲜)细胞具有明显较少的细胞团块,并且还显示出高活力(> 90%)。在所有三种储存溶液中的细胞中观察到活力的时间依赖性降低,除了培养基中细胞之外的簇倾向的任何显着变化。新鲜细胞比其冷冻的对应物更可行,并且生理盐水中的新细胞具有更少的细胞团块。总之,细胞簇和活力可能受到不同细胞制备程序的影响,并且可以使用在动脉内细胞递送之前使用流式细胞术的脉冲宽度测定来进行细胞团聚的定量。

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