Gold Nanoparticle Uptake in Whole Cells in Liquid Examined by Environmental Scanning Electron Microscopy

被引:25
作者
Peckys, Diana B. [1 ]
de Jonge, Niels [1 ,2 ]
机构
[1] INM Leibniz Inst New Mat, Innovat Electron Microscopy Grp, D-66123 Saarbrucken, Germany
[2] Vanderbilt Univ, Med Ctr, Dept Mol Physiol & Biophys, Nashville, TN 37232 USA
关键词
whole cells; environmental scanning electron microscopy; scanning transmission electron microscopy; gold nanoparticles; lysosomes; nanoparticle uptake; nanoparticle size; MAMMALIAN-CELLS; CELLULAR UPTAKE; LIVE CELLS; SIZE; TOXICITY; TRAFFICKING; ENDOSOMES; DELIVERY; RECEPTOR; TISSUES;
D O I
10.1017/S1431927613013986
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The size of gold nanoparticles (AuNPs) can influence various aspects of their cellular uptake. Light microscopy is not capable of resolving most AuNPs, while electron microscopy (EM) is not practically capable of acquiring the necessary statistical data from many cells and the results may suffer from various artifacts. Here, we demonstrate the use of a fast EM method for obtaining high-resolution data from a much larger population of cells than is usually feasible with conventional EM. A549 (human lung carcinoma) cells were subjected to uptake protocols with 10, 15, or 30 nm diameter AuNPs with adsorbed serum proteins. After 20 min, 24 h, or 45 h, the cells were fixed and imaged in whole in a thin layer of liquid water with environmental scanning electron microscopy equipped with a scanning transmission electron microscopy detector. The fast preparation and imaging of 145 whole cells in liquid allowed collection of nanoscale data within an exceptionally small amount of time of similar to 80 h. Analysis of 1,041 AuNP-filled vesicles showed that the long-term AuNP storing lysosomes increased their average size by 80 nm when AuNPs with 30 nm diameter were uptaken, compared to lysosomes of cells incubated with AuNPs of 10 and 15 nm diameter.
引用
收藏
页码:189 / 197
页数:9
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