Abstract

Cellular uptake of hollow casein nanospheres was investigated by confocal microscopy, flow cytometry and transmission electron microscopy. It was found that the casein spheres could enter cellsvia a temperature- or energy-independent mechanism. Confocal microscopy and flow cytometry showed that the cellular uptake amount and velocity of the casein spheres at 4 °C were almost the same as those at 37 °C. Moreover, cellular uptake of casein spheres could not be affected by endocytosis inhibitors, suggesting that a large fraction of casein spheres enter cells in a non-endocytosis fashion. In addition, real-time confocal laser scanning microscopy observation found that the casein spheres first absorbed onto the cell membrane, and then were internalized into the cells mainly through an endocytosis-independent mechanism. Transmission electron microscopy analysis also demonstrated that the casein spheres internalized by cells were mainly distributed in the cytoplasm either at 37 or 4 °C. These findings extend the current understanding of the interactions between milk proteins and biologic systems, and offer a drug nanocarrier which itself has an extraordinary capability to penetrate cell barriers in an energy-independent fashion.

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