Campbell Lia H, Brockbank Kelvin G M
Cell and Tissues Systems, 2231 Technical Parkway, Suite A, North Charleston, SC 29406, USA.
In Vitro Cell Dev Biol Anim. 2007 Sep-Oct;43(8-9):269-75. doi: 10.1007/s11626-007-9039-z. Epub 2007 Sep 19.
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.
随着基于细胞的检测和治疗方法的发展,用于培养和维持细胞的试剂纯度变得更加重要。特别是,使用胎牛血清培养细胞为细胞培养的潜在污染提供了一条直接途径。近年来,许多研究都集中在无血清培养系统的开发上,这不仅是为了缓解由于胎牛血清的可用性和成本带来的困难,也是为了防止潜在致命疾病传播给人类患者。此外,还需要开发用于长期储存细胞库的方法,以降低接触有害疾病的风险。由于大多数方法在其冷冻配方中使用胎牛血清,因此在解冻时避免使用胎牛血清同时能提供同等或更好的细胞回收率的溶液将是理想的。在本研究中,两种血管细胞系作为贴壁细胞群体保存在两种广泛使用的冷冻保护剂——二甲基亚砜和1,2 - 丙二醇中,以及两种赋形剂溶液——Euro - Collins和专门为在低于37摄氏度的温度下维持细胞稳态而配制的Unisol - 冷冻保护剂赋形剂中。还评估了在这些配方中添加血清,以确定其存在是否在冷冻保存期间为细胞提供任何额外的益处。结果表明,使用专为较低温度设计的赋形剂溶液可产生活细胞,其保留的细胞群体活力值高达未冷冻对照的75%。这些结果还表明,在配方中加入血清对细胞没有额外的益处,并且在某些情况下,实际上在冷冻保存后产生了较低的细胞活力。总之,为细胞低温储存设计的溶液的开发为更传统的冷冻保存方案提供了可行的替代方案,并消除了在这些配方中加入血清的必要性。