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Serum-free solutions for cryopreservation of cells

机译:用于细胞冷冻保存的无血清溶液

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With the development of cell-based assays and therapies, the purity of reagents used to grow and maintain cells has become much more important. In particular, the use of fetal calf serum for culturing cells presents a direct path for potential contamination of cell cultures. In recent years, much research has focused on the development of serum-free culturing systems, not only to alleviate difficulties due to availability and cost of fetal calf serum but also to prevent the transmission of potentially fatal diseases to human patients. Additionally, methods need to be developed for long-term storage of cell stocks that also reduce the risk of exposure to harmful diseases. As most methods employ fetal calf serum in their freezing formulations, solutions that avoid the use of fetal calf serum while providing equivalent or better recovery of cells upon thawing would be ideal. In this study, two vascular cell lines have been cryopreserved as adherent cell populations in two widely used cryoprotectants, dimethyl sulfoxide and 1,2-propanediol, and two vehicle solutions, Euro-Collins and Unisol-cryoprotectant vehicle specifically formulated for the maintenance of cell homeostasis at temperatures below 37 degrees C. The addition of serum to these formulations was also evaluated to determine if its presence provided any additional benefit to the cells during cryopreservation. The results demonstrated that using vehicle solutions designed for lower temperatures produced viable cells that retained cell population viability values up to 75% of unfrozen controls. These results also demonstrated that including serum in the formulation provided no additional benefit to the cells and in some cases actually produced lower cell viability after cryopreservation. In conclusion, the development of solutions designed for low-temperature storage of cells provides a viable alternative to more conventional cryopreservation protocols and eliminates the necessity of including serum in these formulations.
机译:随着基于细胞的测定法和疗法的发展,用于生长和维持细胞的试剂的纯度变得越来越重要。特别地,使用胎牛血清培养细胞为细胞培养物的潜在污染提供了直接途径。近年来,许多研究都集中在无血清培养系统的开发上,不仅减轻了因胎牛血清的可获得性和成本而造成的困难,而且还防止了潜在的致命疾病传播给人类患者。另外,需要开发用于长期储存细胞储备的方法,这些方法还可以减少暴露于有害疾病的风险。由于大多数方法在冷冻制剂中使用胎牛血清,因此避免使用胎牛血清同时在融化时提供同等或更好的细胞恢复的解决方案将是理想的。在这项研究中,已将两种血管细胞系冷冻保存为两种广泛使用的冷冻保护剂二甲基亚砜和1,2-丙二醇的粘附细胞群,并专门配制了两种载体溶液Euro-Collins和Unisol-cryoprotectant载体来维持细胞在低于37摄氏度的温度下达到体内稳态。还评估了向这些制剂中添加血清的情况,以确定其存在是否在冷冻保存过程中为细胞提供了其他好处。结果表明,使用设计用于较低温度的媒介物溶液可产生存活的细胞,这些细胞保留的细胞群活力值高达未冷冻对照的75%。这些结果还表明,在制剂中包括血清不会给细胞带来额外的好处,并且在某些情况下,冷冻保存后实际上会产生较低的细胞活力。总之,为低温保存细胞而设计的解决方案的开发为更常规的冷冻保存方案提供了可行的替代方案,并且消除了在这些制剂中包含血清的必要性。

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