Yu Na-Hee, Chun So Young, Ha Yun-Sok, Kim Hyun Tae, Kim Dae Hwan, Kim Jeongshik, Chung Jae-Wook, Lee Jun Nyung, Song Phil Hyun, Yoo Eun Sang, Kim Bum Soo, Kwon Tae Gyun
1Biomedical Research Institute, Kyungpook National University Hospital, 130 Dongdeok-ro, Jung-gu, Daegu, 41944 Korea.
2Department of Urology, School of Medicine, Kyungpook National University, 130 Dongdeok-ro, Jung-gu, Daegu, 41944 Korea.
Tissue Eng Regen Med. 2018 Jul 3;15(5):639-647. doi: 10.1007/s13770-018-0133-y. eCollection 2018 Oct.
The preservation of stem cell viability and characteristics during cell transport from the bench to patients can significantly affect the success of cell therapy. Factors such as suspending medium, time, temperature, cell density, and container type could be considered for transport conditions.
To establish optimal conditions, human amniotic fluid stem cells' (AFSCs) viabilities were analyzed under different media {DMEM(H), DMEM/F-12, K-SFM, RPMI 1640, α-MEM, DMEM(L), PBS or saline}, temperature (4, 22 or 37 °C), cell density (1 × 10 cells were suspended in 0.1, 0.5, 1.0 or 2.0 mL of medium) and container type (plastic syringe or glass bottle). After establishing the transport conditions, stem cell characteristics of AFSCs were compared to freshly prepared cells.
Cells transported in DMEM(H) showed relatively higher viability than other media. The optimized transport temperature was 4 °C, and available transport time was within 12 h. A lower cell density was associated with a better survival rate, and a syringe was selected as a transport container because of its clinical convenience. In compare of stem cell characteristics, the transported cells with established conditions showed similar potency as the freshly prepared cells.
Our findings can provide a foundation to optimization of conditions for stem cell transport.
从实验室到患者的细胞运输过程中,干细胞活力和特性的保存会显著影响细胞治疗的成功率。运输条件可考虑悬浮培养基、时间、温度、细胞密度和容器类型等因素。
为确定最佳条件,在不同培养基{DMEM(H)、DMEM/F-12、K-SFM、RPMI 1640、α-MEM、DMEM(L)、PBS或生理盐水}、温度(4、22或37°C)、细胞密度(1×10个细胞悬浮于0.1、0.5、1.0或2.0 mL培养基中)和容器类型(塑料注射器或玻璃瓶)下分析人羊水干细胞(AFSCs)的活力。确定运输条件后,将AFSCs的干细胞特性与新鲜制备的细胞进行比较。
在DMEM(H)中运输的细胞比其他培养基中的细胞活力相对更高。优化后的运输温度为4°C,有效运输时间在12小时内。较低的细胞密度与更高的存活率相关,由于临床便利性,选择注射器作为运输容器。在比较干细胞特性时,在既定条件下运输的细胞与新鲜制备的细胞显示出相似的效能。
我们的研究结果可为优化干细胞运输条件提供基础。