van der Zwaag Daan, Vanparijs Nane, Wijnands Sjors, De Rycke Riet, De Geest Bruno G, Albertazzi Lorenzo
Department of Pharmaceutics, Ghent University , 9000 Ghent, Belgium.
Inflammation Research Centre, VIB, Ghent, Belgium and Department of Biomedical Molecular Biology, Ghent University , 9052 Ghent, Belgium.
ACS Appl Mater Interfaces. 2016 Mar;8(10):6391-9. doi: 10.1021/acsami.6b00811. Epub 2016 Mar 1.
Understanding the interaction between synthetic nanostructures and living cells is of crucial importance for the development of nanotechnology-based intracellular delivery systems. Fluorescence microscopy is one of the most widespread tools owing to its ability to image multiple colors in native conditions. However, due to the limited resolution, it is unsuitable to address individual diffraction-limited objects. Here we introduce a combination of super-resolution microscopy and single-molecule data analysis to unveil the behavior of nanoparticles during their entry into mammalian cells. Two-color Stochastic Optical Reconstruction Microscopy (STORM) addresses the size and positioning of nanoparticles inside cells and probes their interaction with the cellular machineries at nanoscale resolution. Moreover, we develop image analysis tools to extract quantitative information about internalized particles from STORM images. To demonstrate the potential of our methodology, we extract previously inaccessible information by the direct visualization of the nanoparticle uptake mechanism and the intracellular tracking of nanoparticulate model antigens by dendritic cells. Finally, a direct comparison between STORM, confocal microscopy, and electron microscopy is presented, showing that STORM can provide novel and complementary information on nanoparticle cellular uptake.
了解合成纳米结构与活细胞之间的相互作用对于基于纳米技术的细胞内递送系统的发展至关重要。荧光显微镜是最广泛使用的工具之一,因为它能够在自然条件下对多种颜色进行成像。然而,由于分辨率有限,它不适用于观察单个衍射极限的物体。在这里,我们引入了超分辨率显微镜和单分子数据分析的组合,以揭示纳米颗粒进入哺乳动物细胞过程中的行为。双色随机光学重建显微镜(STORM)能够在纳米尺度分辨率下确定细胞内纳米颗粒的大小和位置,并探测它们与细胞机制的相互作用。此外,我们开发了图像分析工具,以从STORM图像中提取有关内化颗粒的定量信息。为了证明我们方法的潜力,我们通过直接观察纳米颗粒摄取机制和树突状细胞对纳米颗粒模型抗原的细胞内追踪,提取了以前无法获得的信息。最后,对STORM、共聚焦显微镜和电子显微镜进行了直接比较,结果表明STORM可以提供关于纳米颗粒细胞摄取的新颖且互补的信息。