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不同传代比例对MDCK细胞培养效果的影响 被引量:1

Effect of subculture ratio on culture of MDCK cells
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摘要 目的探讨不同传代比例对MDCK细胞培养效果的影响。方法用含10%牛血清的DMEM培养液培养MDCK细胞,按不同传代比例(1∶4、1∶5、1∶6、1∶7、1∶8)连续传5代,观察细胞形态、长势、致密程度,绘制生长曲线,并通过生长动力学方法评价不同传代比例对MDCK细胞培养效果的影响。同时按最佳传代比例于细胞工厂(1层、10层)中进行扩大培养。结果不同传代比例的MDCK细胞均可在48 h增殖至致密单层,细胞生长曲线均趋于"S"型,细胞最大增殖密度均达11×10^4个/cm^2以上。传代比例为1∶8的MDCK细胞平均最大比生长速率显著高于1∶4、1∶5、1∶6的比例(P<0.05),倍增时间显著短于1∶4、1∶5、1∶6、1∶7的比例(P<0.05)。按1∶8的比例在1层和10层细胞工厂中连续传代培养的MDCK细胞生长良好,且稳定。结论按1∶8比例传代的MDCK细胞培养效果最佳。 Objective To investigate the effect of different subculture ratios on the culture of MDCK cells.Methods MDCK cells were cultured in DMEM medium containing 10%bovine serum and subcultured at different subculture ratios(1∶4,1∶5,1∶6,1∶7 and 1∶8)for five passages.The morphology,growth and density of cells were observed,and the growth curve was plotted,based on which the effect of subculture ratio on culture efficiency of MDCK cells was evaluated by growth kinetics analysis.The cells were subjected to expanded culture in cell factories(one and ten layers)at the optimal subculture ratio.Results MDCK cells at different subculture ratios were proliferated to dense monolayer 48 h after subculture,of which the growth curve tended to a S shape,and the maximum proliferation density reached more than 11×10^4 cells/cm^2.The average maximum specific growth rate of MDCK cells at a subculture ratio of 1∶8 was significantly higher than those at 1∶4,1∶5 and 1∶6(P<0.05),while the population doubling time was significantly shorter than those at 1∶4,1∶5,1∶6 and 1∶7(P<0.05).The MDCK cells cultured in one and ten layer cell factories at a subculture ratio of 1∶8 grew well and stably.Conclusion The subculture ratio of 1∶8 was suitable for culture of MDCK cells.
作者 王美皓 李自良 赵彩红 李倬 张雪梅 乔自林 马忠仁 王家敏 WANG Mei-hao;LI Zi-liang;ZHAO Cai-hong;LI Zhuo;ZHANG Xue-mei;QIAO Zi-lin;MA Zhong-ren;WANG Jia-min(Gansu Tech Innovation Center of Animal Cell,Biomedical Research Center,Northwest Minzu University,Lanzhou 730030,Gansu Province,China)
出处 《中国生物制品学杂志》 CAS CSCD 2020年第11期1230-1234,1239,共6页 Chinese Journal of Biologicals
基金 国家科技重大专项重大新药创制项目(2015ZX09102016) 西北民族大学动物细胞培养与代谢工程创新团队(319201-90004) 甘肃省重点研发计划(18YF1FA121)。
关键词 MDCK细胞 传代培养 生长曲线 MDCK cells Subculture Growth curve
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  • 1周龙,陈曦,罗宗平,杨惠林,何帆.C57BL/6小鼠骨髓单核细胞分离、培养、纯化及向破骨细胞的分化[J].中国组织工程研究,2015,19(6):940-944. 被引量:9
  • 2卢建红,邵卫星,龙进学,刘玉良,石火英,刘秀梵.H9N2禽流感病毒反向遗传系统转录/表达载体的构建和验证[J].中国病毒学,2005,20(4):388-392. 被引量:5
  • 3王佃亮,肖成祖,陈昭烈,黄子才.微载体高密度培养Vero细胞的研究[J].生物工程学报,1996,12(2):164-170. 被引量:22
  • 4Madin SH, Darby JNB. Established kidney cell lines of normal adult bovine and ovine origin. Proc Soc Exp Biol Med, 1958, 98(3): 574-576. 被引量:1
  • 5Rodgers SE, Barton ES, Oberhaus SM, et al. Reovirus-induced apoptosis of MDCK cells is not linked to viral yield and is blocked by Bcl-2. J Virol, 1997, 71: 2540-2546. 被引量:1
  • 6Mochizuki M. Growth characteristics of canine pathogenic viruses in MDCK cells cultured in RPMI 1640 medium without animal protein. Vaccine, 2006, 24:1744 1748. 被引量:1
  • 7Mochizuki M, Hashimoto T. Growth of feline panlenkopenia vius and canine parvovirus in vitro. Jpn J Vet Sci, 1996, 48(4): 841-844. 被引量:1
  • 8Subbarao K, Klimov A, Jacqueline Katz, et al.Characterization of an avian influenza A (H5N1) virus isolated from a child with a fatal respiratory illness. Science, 1998, 279:393-396. 被引量:1
  • 9Tree JA, Richardson C, Fooks AR, et al. Comparison of large-scale mammalian cell culture systems with egg culture for the production of influenza virus A vaccine strains. Vaccine, 2001, 19: 3444-3450. 被引量:1
  • 10Genzel Y, Reichl U. Continuous cell lines as a production system for influenza vaccines. Expert Rev Vaccine. 2009, 8(12): 1681-1692. 被引量:1

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