Department of Electrical and Computer Engineering, University of Utah, Salt Lake City, Utah 84112, USA.
Int J Hyperthermia. 2012;28(2):163-74. doi: 10.3109/02656736.2011.638963.
The goal is to identify thermal exposures capable of reducing or eliminating cell survival on expanded polytetrafluoroethylene (ePTFE), in an effort to develop a mild hyperthermia treatment of neointimal hyperplasia in ePTFE vascular grafts.
Viable and dead bovine aortic endothelial cells were quantified following different thermal exposure conditions: cells on collagen-coated ePTFE sheets or tissue culture polystyrene dishes were heated at 42° and 45°C to determine their thermal sensitivity on different surfaces, and cells cultured on collagen-coated ePTFE sheets were heated at 43-50°C for various durations, followed by incubation at 37°C for 0 and 20 h, respectively. Significant cell death was set to be 50%. Two types of cell death, apoptosis and necrosis, were distinguished by cell morphology and membrane integrity assessments.
The attachment and survival of cells on ePTFE sheets were more sensitive to inhibition by mild heating than those on tissue culture dishes. Exposure to 45°C for 90 min and 50°C for 30 min caused significant necrotic cell death on ePTFE (65% and 75%, respectively). A 37°C/20-h incubation following 30-min exposures at 47° and 50°C increased total cell death (necrosis + apoptosis) from 20% to 50% and 75% to 100%, respectively.
Cells grown on ePTFE were more susceptible to mild hyperthermia-induced death, compared to those on tissue culture dishes. Significant cell death on ePTFE mainly via apoptosis can be achieved by optimising temperature and duration of exposure.
旨在确定能够降低或消除 ePTFE(膨胀聚四氟乙烯)上细胞存活率的热暴露条件,以开发一种用于 ePTFE 血管移植物内膜增生的温和热疗方法。
对不同热暴露条件下的存活和死亡牛主动脉内皮细胞进行定量:将细胞接种于涂有胶原蛋白的 ePTFE 片或组织培养聚苯乙烯培养皿上,分别在 42°C 和 45°C 下加热,以确定在不同表面上的热敏感性,以及将细胞接种于涂有胶原蛋白的 ePTFE 片上,在 43-50°C 下加热不同时间,随后在 37°C 下分别孵育 0 和 20 h。设定显著细胞死亡为 50%。通过细胞形态和膜完整性评估来区分两种细胞死亡方式,即凋亡和坏死。
与组织培养皿相比,ePTFE 片上细胞的附着和存活对温和加热的抑制更为敏感。暴露于 45°C 90 min 和 50°C 30 min 可导致 ePTFE 上发生显著的坏死性细胞死亡(分别为 65%和 75%)。在 47°C 和 50°C 下暴露 30 min 后,在 37°C 下孵育 20 h 会使总细胞死亡(坏死+凋亡)分别从 20%增加至 50%和从 75%增加至 100%。
与组织培养皿相比,生长在 ePTFE 上的细胞对温和热诱导的死亡更为敏感。通过优化温度和暴露时间,可以实现 ePTFE 上主要通过凋亡的显著细胞死亡。