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鄢祝兵, 马勇杰, 古宏晨, 童乃虎, 徐宏. 肺腺癌细胞对谷胱甘肽纳米Fe3O4的内吞作用[J]. 中国公共卫生, 2007, 23(1): 47-49. DOI: 10.11847/zgggws2007-23-01-28
引用本文: 鄢祝兵, 马勇杰, 古宏晨, 童乃虎, 徐宏. 肺腺癌细胞对谷胱甘肽纳米Fe3O4的内吞作用[J]. 中国公共卫生, 2007, 23(1): 47-49. DOI: 10.11847/zgggws2007-23-01-28
YAN Zhu-bing, MA Yong-jie, GU Hong-chen, . Endocytosis of lung adenocarcinoma cell on glutathione modified magnetite(Fe3O4)nanoparticles[J]. Chinese Journal of Public Health, 2007, 23(1): 47-49. DOI: 10.11847/zgggws2007-23-01-28
Citation: YAN Zhu-bing, MA Yong-jie, GU Hong-chen, . Endocytosis of lung adenocarcinoma cell on glutathione modified magnetite(Fe3O4)nanoparticles[J]. Chinese Journal of Public Health, 2007, 23(1): 47-49. DOI: 10.11847/zgggws2007-23-01-28

肺腺癌细胞对谷胱甘肽纳米Fe3O4的内吞作用

Endocytosis of lung adenocarcinoma cell on glutathione modified magnetite(Fe3O4)nanoparticles

  • 摘要: 目的在体外观察人肺腺癌细胞(SPC-A1)对谷胱甘肽(GSSG)修饰的纳米Fe3O4的内吞作用及与培养温度、时间及浓度的关系。方法通过透射电镜(TEM)与普鲁士兰染色法观察SPC-A1细胞对GSSG修饰的纳米Fe3O4的内吞作用。采用原子吸收光谱(AAS)法进行SPC-A1细胞粘附量及内吞量的定量分析。结果TEM结果表明,在4℃下培养24 h后GSSG修饰的纳米Fe3O4吸附于SPC-A1细胞表面;37℃下培养1 h后SPC-A 1细胞可内吞GSSG修饰的纳米Fe3O4细胞数目明显增加。AAS分析表明,SPC-A1细胞表面纳米Fe3O4的粘附量同培养时间及浓度呈正相关。GSSG修饰的纳米Fe3O4浓度较低(0.1或0.4 mg/ml)时,内吞量在24 h后达到饱和;GSSG修饰的纳米Fe3O4浓度较高(0.7或1.0 mg/ml)时,内吞量在72 h后达到饱和,单个细胞内吞量最大可达160 pg。结论SPC-A1细胞对GSSG修饰的纳米Fe3O4的内吞需要能量,内吞量依赖于浓度及培养时间。

     

    Abstract: ObjectiveTo study the relationship between endocy tosis of human lung adenocarcinoma cell line SPC-A1 modified by ox idized Glutathione(GSSG)and culture conditions including culture temperature,time and concentration.MethodThe uptake of GSSG-modified Fe3O4 nanoparticles by SPC-A1 cell was observed by transmission electron microscopy (TEM)and Prussian blue staining.The extracellular adhesion or intracellular uptake of GSSG-modified Fe3O4 nanoparticles were measured by atom absorb spectrum(AAS).ResultsTEM results indicated that GSSG-modified Fe3O4 nanoparticles adhered on the membrane of SPC-A1 cell after being cultured at 4℃ for 1 h or 24 h,but SPC-Al cell could took up nanoparticles particles after cultured at 37℃ for 1 h.Prussian blue staining indicated that SPC-Al cells containing GSSG-modified Fe3O4 nanoparticles were much more with the pro longation of culture time or the increase of concentration.AAS analysis indicated that the extracellular adhesion of GSSG-modified magnetic particles was depended on culture time and concentration.The uptake amount of GSSG-modiied Fe3O4 nanoparticles by SPC-A1 cell was saturated after 24 h when the nanoparticles in low concentration(0.1 mg/ml or 0.4 mg/ml),the uptake was saturated after 72 h when the nano particles in high concentration(0.7 mg/ml or 1.0 mg/ml).The maximal amount per SPC-A1 cell could reach 160 pg.ConclusionThe uptake of GSSG-modified Fe3O4 nanoparticles by SPC-A1 cell is energy needed.It depends on the concentration of nanopar ticles and saturates at certain time.

     

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