文章摘要
刘彦陈绍良△ 徐祖玲刘志忠阚静毛文星.大鼠主动脉内皮细胞的分离培养和鉴定[J].,2014,14(5):834-836
大鼠主动脉内皮细胞的分离培养和鉴定
Isolation Culture and Identification of Rat Aortic Endothelial Cells
  
DOI:
中文关键词: 大鼠  主动脉内皮细胞  培养  鉴定  复苏
英文关键词: Rat  Aortic endothelial cells  Culture  Identify  Recovery
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作者单位
刘彦陈绍良△ 徐祖玲刘志忠阚静毛文星 南京医科大学附属南京医院心内科、南京市第一医院 
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中文摘要:
      摘要目的:探索大鼠主动脉原代内皮细胞体外培养方法,为体外研究提供细胞模型。方法:分离大鼠主动脉,直接贴壁于培养皿 中,荧光倒置显微镜观察细胞形态,免疫组化Ⅷ因子相关抗原染色鉴定细胞。结果:约24 小时组织块边缘有游离的新生细胞长 出,7天即融合成片。消化传代后细胞呈短梭形或三角形,单层生长,铺路石状,Ⅷ因子表达阳性,呈指数增殖。冻存后复苏细胞活 性均超过90%。结论:用贴壁法成功建立了大鼠血管内皮细胞体外培养方法,冻存细胞存活率高,为体外研究提供了稳定的模型。
英文摘要:
      ABSTRACT Objective:To investigate the culture methods of primary rat aortic endothelial cells in vitro.Methods: Rat aorta was isolated, directly attached to the wall in a petri dish, and inverted microscope cell morphology. Immunohistochemistry factor VIII-related antigen was used to stain cells. Results:Organization block edge free new cells grow, after approximately 24, and integrated into the film 7d later. Cells were subcultured short spindle-shaped or triangular, monolayer, cobblestone, positive expression of factor VIII, the exponential proliferation. Recovery was more than 90% cell viability after cryopreservation. Conclusion:Vascular endothelial cells in vitro method was successfully established by adherent, and the survival rate of frozen cells was high, which providing a stable model for in vitro studies.
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