Comparative evaluation of nano-CuO crossing Caco-2 cell monolayers and cellular uptake

被引:3
|
作者
Gao Chen [1 ,2 ,3 ]
Zhu Lianqin [1 ]
Zhu Fenghua [1 ]
Zheng Fang [2 ]
Song Mingming [1 ]
Huang Kai [1 ]
机构
[1] Qingdao Agr Univ, Coll Anim Sci & Vet Med, Qingdao 266109, Peoples R China
[2] Dezhou Univ, Coll Agr, Dezhou 253023, Peoples R China
[3] Jilin Univ, Coll Vet Med, Changchun 130062, Peoples R China
基金
中国国家自然科学基金;
关键词
Nano-CuO; Caco-2; cell; Apparent permeability coefficient; Endocytotic pathway; Inhibitors of endocytosis; Nanobiotechnology; MEDIATED ENDOCYTOSIS; OXIDE NANOPARTICLES; CARBON NANOTUBES; PATHWAY; DELIVERY; RELEASE; ACTIN;
D O I
10.1007/s11051-015-3005-6
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Different concentrations of CuSO4, micro-CuO, and nano-CuO were added to Caco-2 cell monolayers to study the absorption and transport characteristics in this epithelial cell model. Nano-CuO nanoparticles had a diameter of 10-20 nm. Inhibitors of endocytosis were used to explore whether nano-CuO could enter the Caco-2 cell in the form of nanoparticles, and to ascertain the endocytotic pathway that is involved in the transport process. The apparent permeability coefficient (P-app) of CuSO4 and nano-CuO increased with the Cu concentration in the culture medium (p < 0.05). The micro-CuO of different concentrations had no significant impact on the P-app value of Caco-2 cells (p > 0.05). When the Cu concentration in the culture medium was in the range 31.25-500 mu M, the P-app value of Caco-2 cells incubated with nano-CuO was significantly higher than that obtained with CuSO4. The latter was also significantly higher than that when cells were incubated with micro-CuO (p < 0.05). The amount of Cu transport increased with the increase of CuSO4 concentration in the culture medium. After 90 min, the amount of transport began to saturate, and the transport rate of Cu declined with the increase of CuSO4 concentration. For the cells incubated with nano-CuO, the amount of Cu transport increased with the increase of nano-CuO concentration, but did not show an obvious saturation with the extension of transport time. Nano-CuO could enter the Caco-2 cell in the form of nanoparticles, and were found in the cytoplasm, vesicles, lysosomes, and cell nuclei. Several inhibitors of endocytosis effectively prevented the entry of nano-CuO into the Caco-2 cells. It was concluded that nano-CuO particles can enter the Caco-2 cells through several cellular endocytotic pathways.
引用
收藏
页数:10
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