Jo Hong Li, Song Yo Han, Park Jinho, Jo Eun-Jung, Goh Yeongchang, Shin Kyujin, Kim Min-Gon, Lee Kang Taek
Department of Chemistry, Gwangju Institute of Science and Technology (GIST), Gwangju 500-712, Korea.
Nanoscale. 2015 Dec 14;7(46):19397-402. doi: 10.1039/c5nr05875a.
We report on the development of a three-dimensional (3D) live-cell imaging technique with high spatiotemporal resolution using lanthanide-doped upconverting nanoparticles (UCNPs). It employs the sectioning capability of confocal microscopy except that the two-dimensional (2D) section images are acquired by wide-field epi-fluorescence microscopy. Although epi-fluorescence images are contaminated with the out-of-focus background in general, the near-infrared (NIR) excitation used for the excitation of UCNPs does not generate any autofluorescence, which helps to lower the background. Moreover, the image blurring due to defocusing was naturally eliminated in the image reconstruction process. The 3D images were used to investigate the cellular dynamics such as nuclear uptake and single-particle tracking that require 3D description.
我们报告了一种使用镧系元素掺杂的上转换纳米粒子(UCNPs)开发的具有高时空分辨率的三维(3D)活细胞成像技术。它采用了共聚焦显微镜的切片能力,不同的是二维(2D)切片图像是通过宽场落射荧光显微镜采集的。尽管落射荧光图像通常会受到离焦背景的污染,但用于激发UCNPs的近红外(NIR)激发不会产生任何自发荧光,这有助于降低背景。此外,在图像重建过程中自然消除了由于离焦导致的图像模糊。3D图像用于研究需要三维描述的细胞动力学,如核摄取和单粒子跟踪。