Ng Cheng Teng, Tang Florence Mei Ai, Li Jasmine Jia'en, Ong Cynthia, Yung Lanry Lin Yue, Bay Boon Huat
Department of Anatomy, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Anat Rec (Hoboken). 2015 Feb;298(2):418-27. doi: 10.1002/ar.23051. Epub 2014 Oct 3.
Gold nanoparticles (AuNPs) have potential biomedical and scientific applications. In this study, we evaluated the uptake and internalization of FBS-coated 20 nm AuNPs into lung fibroblasts and liver cells by different microscopy techniques. AuNP aggregates were observed inside MRC5 lung fibroblasts and Chang liver cells under light microscopy, especially after enhancement with automegallography. Clusters of AuNPs were observed to be adsorbed on the cell surface by scanning electron microscopy. Ultrathin sections showed that AuNPs were mainly enclosed within cytoplasmic vesicles when viewed under transmission electron microscopy. We also investigated the mechanism of uptake for AuNPs, using endocytosis inhibitors and quantification of Au with inductively coupled plasma mass spectrometry. Cells treated with concanavalin A and chlorpromazine showed significant decrease of Au uptake in MRC5 lung fibroblasts and Chang liver cells, respectively, implying that the uptake of AuNPs was facilitated by clathrin-mediated endocytosis. It would therefore appear that uptake of 20 nm AuNPs in both cell types with different tissues of origin, was dependent upon clathrin-mediated endocytosis.
金纳米颗粒(AuNPs)具有潜在的生物医学和科学应用价值。在本研究中,我们通过不同的显微镜技术评估了胎牛血清包被的20纳米金纳米颗粒被肺成纤维细胞和肝细胞摄取及内化的情况。在光学显微镜下,尤其是经过自动显影增强后,在MRC5肺成纤维细胞和Chang肝细胞内观察到了金纳米颗粒聚集体。通过扫描电子显微镜观察到金纳米颗粒簇吸附在细胞表面。超薄切片显示,在透射电子显微镜下观察时,金纳米颗粒主要被包裹在细胞质小泡内。我们还使用内吞作用抑制剂并通过电感耦合等离子体质谱法定量金,研究了金纳米颗粒的摄取机制。用伴刀豆球蛋白A和氯丙嗪处理的细胞分别在MRC5肺成纤维细胞和Chang肝细胞中显示出金摄取的显著减少,这意味着网格蛋白介导的内吞作用促进了金纳米颗粒的摄取。因此,似乎起源于不同组织的两种细胞类型对20纳米金纳米颗粒的摄取均依赖于网格蛋白介导的内吞作用。