Centre Hospitalier Universitaire Vaudois & University of Lausanne, Lausanne, Switzerland.
Nanomedicine (Lond). 2010 Sep;5(7):1075-87. doi: 10.2217/nnm.10.79.
Ultrasmall superparamagnetic iron oxide nanoparticles (USPIONs) are currently under development for the intracellular delivery of therapeutics. However, the mechanisms of cellular uptake and the cellular reaction to this uptake, independent of therapeutics, are not well defined. The interactions of biocompatible cationic aminoUSPIONs with human cells was studied in 2D and 3D cultures using biochemical and electron microscopy techniques. AminoUSPIONs were internalized by human melanoma cells in 2D and 3D cultures. Uptake was clathrin mediated and the particles localized in lysosomes, inducing activation of the lysosomal cathepsin D and decreasing the expression of the transferrin receptor in human melanoma cells and/or skin fibroblasts. AminoUSPIONs deeply invaded 3D spheroids of human melanoma cells. Thus, aminoUSPIONs can invade tumors and their uptake by human cells induces cell reaction.
超顺磁性氧化铁纳米颗粒(USPIONs)目前正在开发用于治疗药物的细胞内递送。然而,细胞摄取的机制以及独立于治疗药物的细胞反应尚未得到很好的定义。使用生化和电子显微镜技术研究了生物相容性阳离子 USPIONs 与人细胞的相互作用。氨基酸 USPIONs 被二维和三维培养的人黑色素瘤细胞内化。摄取是网格蛋白介导的,颗粒定位于溶酶体中,诱导溶酶体组织蛋白酶 D 的激活,并降低人黑色素瘤细胞和/或皮肤成纤维细胞中转铁蛋白受体的表达。氨基酸 USPIONs 深入侵入人黑色素瘤细胞的 3D 球体。因此,氨基酸 USPIONs 可以侵入肿瘤,其被人细胞摄取会诱导细胞反应。