Leoni P, Olivieri A, Centurioni R, Montillo M
Boll Soc Ital Biol Sper. 1983 Aug 30;59(8):1089-95.
Ten bone marrow suspensions have been cryopreserved by a Programmed Freezer Planer R 201. Total cellularity, viability, differential myelograms, cytochemical pattern and CFU-GM growth "in vitro", have been evaluated on the cellular suspensions both before and after 1 and 18 months of storage in liquid nitrogen. Total cellular recovery and viable cell recovery were satisfactory, cellular loss being due, almost entirely to death of the more mature cells. NASDA reaction did not vary after freezing, on the contrary peroxidase reaction and overall PAS reaction showed respectively a slight and an almost complete disappearance. LAP reaction was not valuable, after freezing, because of the more mature myeloid cell loss. CFU-GM recovery was satisfactory and clusters and colonies growth in methylcellulose appeared quite similar before and after 1 and 18 months of storage at very low temperature. Our cryopreservation technique cannot prevent some cellular loss or some qualitative cellular damage, but colonizing ability is almost completely preserved.
采用程序冷冻仪R 201对10份骨髓悬液进行了冷冻保存。在液氮中储存1个月和18个月前后,对细胞悬液的总细胞数、活力、骨髓细胞分类计数、细胞化学模式以及体外CFU-GM生长情况进行了评估。总细胞回收率和活细胞回收率令人满意,细胞损失几乎完全是由于较成熟细胞的死亡。冷冻后NASDA反应没有变化,相反,过氧化物酶反应和总的PAS反应分别略有消失和几乎完全消失。由于较成熟的髓细胞损失,冷冻后LAP反应没有价值。CFU-GM回收率令人满意,在非常低温下储存1个月和18个月前后,甲基纤维素中的集落和集簇生长看起来非常相似。我们的冷冻保存技术不能防止一些细胞损失或一些细胞质量损伤,但定植能力几乎完全得以保留。