Center for Stem Cell and Regenerative Medicine, Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo, 113-8510, Japan.
Department of Cartilage Regeneration, Tokyo Medical and Dental University, Tokyo, Japan.
BMC Musculoskelet Disord. 2019 Jul 6;20(1):316. doi: 10.1186/s12891-019-2700-3.
Synovial mesenchymal stem cells (MSCs) are an attractive cell source for cartilage and meniscus regeneration. The optimum cryopreservation medium has not been determined, but dimethylsulfoxide (DMSO) should be excluded, if possible, because of its toxicity. The purposes of our study were to examine the possible benefits of higher concentrations of serum and the effectiveness of 100% serum (without DMSO) for the cryopreservation of synovial MSCs.
Human synovium was harvested from the knees of four donors with osteoarthritis during total knee arthroplasty. Synovial MSCs (8 × 10 cells) were suspended in 400 μL medium and used as a Time 0 control. The same number of synovial MSCs was also suspended in 400 μL α-MEM medium containing 10% fetal bovine serum (FBS) (5% DMSO, and 1% antibiotic), 95% FBS (and 5% DMSO), or 100% FBS (no DMSO) and cryopreserved at - 80 °C for 7 days. After thawing, the cell suspensions (1.5 μL; 3 × 10 cells) were cultured in 60 cm dishes for 14 days for colony formation assays. Additional 62.5 μL samples of cell suspensions (1.25 × 10 cells) were added to tubes and cultured for 21 days for chondrogenesis assays.
Colony numbers were significantly higher in the Time 0 and 95% FBS groups than in the 10% FBS group (n = 24). Colony numbers were much lower in the 100% FBS group than in the other three groups. The cell numbers per dish reflected the colony numbers. Cartilage pellet weights were significantly heavier in the 95% FBS group than in the 10% FBS group, whereas no difference was observed between the Time 0 and the 95% FBS groups (n = 24). No cartilage pellets formed at all in the 100% FBS group.
Synovial MSCs cryopreserved in 95% FBS with 5% DMSO maintained their colony formation and chondrogenic abilities to the same levels as observed in the cells before cryopreservation. Synovial MSCs cryopreserved in 100% FBS lost their colony formation and chondrogenic abilities.
滑膜间充质干细胞(MSCs)是软骨和半月板再生的有吸引力的细胞来源。尚未确定最佳的冷冻保存介质,但如果可能的话,应排除二甲基亚砜(DMSO),因为它具有毒性。我们研究的目的是检查高浓度血清的可能益处,以及 100%血清(无 DMSO)对滑膜 MSCs 冷冻保存的有效性。
在全膝关节置换术期间,从 4 位患有骨关节炎的供体的膝关节中采集滑膜。将 8×10 个滑膜 MSCs(细胞)悬浮在 400μL 培养基中,并作为时间 0 对照。相同数量的滑膜 MSCs 也悬浮在含有 10%胎牛血清(FBS)的 400μL α-MEM 培养基中(5%DMSO 和 1%抗生素),95%FBS(和 5%DMSO)或 100%FBS(无 DMSO),并在-80°C 下冷冻保存 7 天。解冻后,将细胞混悬液(1.5μL;3×10 个细胞)接种于 60cm 培养皿中进行 14 天的集落形成测定。将另外 62.5μL 细胞混悬液(1.25×10 个细胞)添加到试管中,并培养 21 天进行软骨形成测定。
时间 0 和 95%FBS 组的集落数明显高于 10%FBS 组(n=24)。100%FBS 组的集落数明显低于其他三组。每个培养皿中的细胞数量反映了集落数。95%FBS 组的软骨球重量明显高于 10%FBS 组,而时间 0 组和 95%FBS 组之间无差异(n=24)。100%FBS 组根本没有形成软骨球。
在含有 5%DMSO 的 95%FBS 中冷冻保存的滑膜 MSCs 保持其集落形成和软骨生成能力与冷冻保存前的细胞相同。在 100%FBS 中冷冻保存的滑膜 MSCs 丧失了其集落形成和软骨生成能力。