Improved Hypothermic Preservation of Human Renal Cells Through Suppression of Both Apoptosis and Necrosis

碘化丙啶 膜联蛋白 细胞凋亡 冷库 高架桥 坏死 程序性细胞死亡 低温保存 细胞生物学 男科 化学 生物 生物化学 医学 内科学 园艺 胚胎
作者
Aby J. Mathew,Robert G. Van Buskirk,John G. Baust
出处
期刊:Cell Preservation Technology [Mary Ann Liebert]
卷期号:1 (4): 239-253 被引量:33
标识
DOI:10.1089/15383440260682071
摘要

A new platform of hypothermic solutions, the HypoThermosol® (HTS) series, has been developed for the improved hypothermic storage of cells, tissues, and organs. Cells and tissues cold-stored in HTS-FRS demonstrate improved viability when returned to normothermic temperatures in comparison with the parent solution, HTS-BASE, or University of Wisconsin (UW) solution (UW-ViaSpan®). While our group and others have implicated apoptosis as a major player in cell death initiated by extended hypothermic storage, it has been unclear if the improved performance of HTS-FRS as a hypothermic storage solution is due to its ability to inhibit apoptosis. Data reported herein show that human renal cells hypothermically stored in renal cell culture medium, HTS-FRS, HTS-BASE, or UW solution demonstrated improved survival in HTS-FRS. Following 5 days of hypothermic preservation and 1 day of recovery at 37°C, cells preserved in HTS-FRS exhibit 75% metabolic activity, whereas cells stored in HTS-BASE, UW, or culture media demonstrate 32%, 17%, and 6% recovery, respectively. In addition, cells stored in HTS-BASE supplemented with caspase inhibitor exhibit increased cell numbers in comparison to cells stored in HTS-BASE (72% vs. 30% after 7 days of cold storage and 2 days of recovery). Experiments with annexin and propidium iodide as well as assessment of caspase activities suggest that the improved performance of HTS-FRS as a preservation solution may be due to its ability to inhibit both apoptosis and necrosis.
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