Hubel Allison, Spindler Ralf, Curtsinger Julie M, Lindgren Bruce, Wiederoder Sara, McKenna David H
Biopreservation Core Resource, University of Minnesota, Minneapolis, Minnesota.
Mechanical Engineering Department, University of Minnesota, Minneapolis, Minnesota.
Transfusion. 2015 May;55(5):1033-9. doi: 10.1111/trf.12971. Epub 2014 Dec 19.
The continued growth in the uses of umbilical cord blood (UCB) will require the development of meaningful postthaw quality assays. This study examines both conventional and new measures for assessing UCB quality after long-term storage.
The first arm of the study involved thawing UCB in storage for short (approx. 1 year) and long periods of time (>11 years). Conventional postthaw measures (colony-forming units [CFU], total nucleated cell counts, CD34+45+) were quantified in addition to apoptosis. The second arm of the study involved taking units stored in liquid nitrogen and imposing a storage lesion by storing the units in -80°C for various periods of time. After storage lesion, the units were thawed and assessed.
In the first arm of the study, there was little difference in the postthaw measures between UCB stored for short and long periods of time. There was a slight increase in the percentage of CD34+45+ cells with time in storage and a reduction in the number of cells expressing apoptosis markers. When moved from liquid nitrogen to -80°C storage, the nucleated cell count varied little but there was a distinct decrease in frequency of CFUs and increase in percentage of cells expressing both early and late markers of apoptosis.
Nucleated cell counts do not reflect damage to hematopoietic progenitors during long-term storage. Expression of caspases and other markers of apoptosis provide an early biomarker of damage during storage, which is consistent with other measures such as CFU and percentage of CD34+45+ cells.
脐带血(UCB)使用量的持续增长将需要开发有意义的解冻后质量检测方法。本研究考察了评估长期储存后UCB质量的传统方法和新方法。
研究的第一部分涉及解冻短期(约1年)和长期(>11年)储存的UCB。除了细胞凋亡外,还对解冻后的传统检测指标(集落形成单位[CFU]、总核细胞计数、CD34+45+)进行了定量分析。研究的第二部分涉及取出储存在液氮中的样本,并通过在-80°C下储存不同时间段来造成储存损伤。造成储存损伤后,将样本解冻并进行评估。
在研究的第一部分中,短期和长期储存的UCB解冻后检测指标差异不大。随着储存时间的延长,CD34+45+细胞的百分比略有增加,而表达凋亡标志物的细胞数量减少。当从液氮转移到-80°C储存时,有核细胞计数变化不大,但CFU频率明显降低,同时表达早期和晚期凋亡标志物的细胞百分比增加。
有核细胞计数不能反映长期储存期间造血祖细胞的损伤情况。半胱天冬酶和其他凋亡标志物的表达提供了储存期间损伤的早期生物标志物,这与CFU和CD34+45+细胞百分比等其他检测指标一致。