Nazarpour Robab, Zabihi Ebrahim, Alijanpour Ebrahim, Abedian Zeinab, Mehdizadeh Hamid, Rahimi Fatemeh
Cellular and Molecular Biology Research Center, Babol University of Medical Sciences, Babol, Iran. ; Department of Anesthesiology, Roohani Hospital, Babol University of Medical Sciences, Babol, Iran.
Cellular and Molecular Biology Research Center, Babol University of Medical Sciences, Babol, Iran. ; Department of Pharmacology & Physiology, School of Medicine, Babol University of Medical Sciences, Babol, Iran.
Int J Mol Cell Med. 2012 Spring;1(2):88-93.
Cryopreservation is the method of choice for long term storage of human PBMCs. This study was designed to compare the different combinations of variables affecting the cryopreservation of PBMCs samples. The viability of PBMCs separated from 2×5 ml peripheral blood samples obtained from 16 healthy adult volunteers, were measured using trypan blue dye exclusion method just before freezing with different concentrations of DMSO (10, 15, and 20%) and FBS (40 or 70%) at two different temperatures (either 4(o)C or 25(o)C). Then after 2 weeks the cells were thawed and the viability was measured again. Also the PBMCs response to PHA was measured after 48 h using MTT assay. The effects of the different variables were calculated and compared among the groups. A total of 192 PBMCs cryotubes made from blood samples of 16 volunteers were tested. The viability of the cells obtained by the two centrifugation procedure was the same (both more than 99%). The concentration of the FBS (40 vs 70%) did not show to have significant effects on either cells viability or response to PHA. On the other hand 20% DMSO concentration and freezing temperature at 25(o)C decreased both cells. Based on the obtained results, it is recommended to centrifuge the PBMCs under higher revolt speed at shorter time (700 g for 20 minutes) and decrease the FBS concentration to 40%. The DMSO concentration should be kept at 10-15% and the freezing medium be cooled down to 4(o)C.
低温保存是长期储存人外周血单个核细胞(PBMCs)的首选方法。本研究旨在比较影响PBMCs样本低温保存的不同变量组合。从16名健康成年志愿者采集的2×5 ml外周血样本中分离出的PBMCs,在分别用不同浓度的二甲基亚砜(DMSO,10%、15%和20%)和胎牛血清(FBS,40%或70%),于两个不同温度(4℃或25℃)冷冻之前,使用台盼蓝染料排除法测量其活力。然后在2周后将细胞解冻并再次测量活力。此外,在48小时后使用MTT法测量PBMCs对PHA的反应。计算并比较不同组之间不同变量的影响。总共测试了由16名志愿者的血样制成的192个PBMCs冷冻管。通过两种离心程序获得的细胞活力相同(均超过99%)。FBS浓度(40%对70%)对细胞活力或对PHA的反应均未显示出显著影响。另一方面,20%的DMSO浓度和25℃的冷冻温度会使两种细胞活力均下降。根据所得结果,建议以较高转速在较短时间内(700 g,20分钟)离心PBMCs,并将FBS浓度降至40%。DMSO浓度应保持在10 - 15%,冷冻培养基冷却至4℃。