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机构地区:[1]暨南大学第一临床医院眼科,广东省广州市510632 [2]暨南大学第三附属医院眼科,广东省广州市519000 [3]暨南大学医学院眼科教研室,广东省广州市510632
出 处:《中国组织工程研究与临床康复》2012年第5期867-870,共4页Journal of Clinical Rehabilitative Tissue Engineering Research
基 金:珠海市科技计划资助项目(PB20051014)~~
摘 要:背景:传统的细胞冻存多采用4,-20℃放置的阶梯式降温方法,程序复杂且浪费时间。目的:比较传统法与改良冻存法对血管内皮细胞的保护效果。方法:将常规培养的人血管内皮细胞用胰酶消化后,用配置好的冻存液(10%二甲基亚砜、体积分数60%胎牛血清、30%DMEM无血清培养基)调整浓度,将细胞悬液吸入冻存管,分组干预:实验组以纱布包裹,并直接投入-80℃冰箱;对照组按常规冻存法,4℃冰箱和-20℃冰箱分别预冷30min和1h后放入-80℃冰箱。1个月后快速复苏冻存细胞。结果与结论:复苏后实验组细胞存活率及生长曲线与对照组比较差异无显著性意义;复苏后实验组细胞贴壁率、形态学变化及增殖能力明显优于对照组。说明改良的纱布包裹法优于传统的细胞冻存法,且更加方便快捷。BACKGROUND:As for traditional cryopreserving method,cells are cooling by steps at 4 ℃ and-20 ℃,which is complicated and a waste of time.OBJECTIVE:To compare the protective effects of traditional and reforming cryopreserving methods on human vascular endothelial cells.METHODS:The vascular endothelial cells were incubated with a freezing medium consisting of 10% dimethyl sulfoxide,60% fetal bovine serum and 30% DMEM serum-free medium after digested with trypsin,and then the cell suspension were put into preserving tubes.Each group was intervened.In the experimental group,the tubes were packaged with gauze and then thawed into-80 ℃ refrigerator straightly.In the control group,the tubes were pre-cooling at 4 ℃ and-20 ℃ for 30 minutes and 1 hour,then thaw into-80 ℃ refrigerator.One month later,the endothelial cells were resuscitated.RESULTS AND CONCLUSION:There were no significant difference in the survival rates and growth curves between experimental group and control group.The experimental group was significantly better than control group in adherence rates,morphological changes and proliferation.The reforming cryopreserving method is better than traditional cryopreserving method which is more convenient and easier to operate.
分 类 号:R318[医药卫生—生物医学工程]
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