Chowdhury Shwetadwip, Eldridge Will J, Wax Adam, Izatt Joseph A
Department of Biomedical Engineering, Fitzpatrick Institute for Photonics, 1427 FCIEMAS, 101 Science Drive Box 90281, Durham, North Carolina 27708, USA.
Biomed Opt Express. 2017 Nov 28;8(12):5776-5793. doi: 10.1364/BOE.8.005776. eCollection 2017 Dec 1.
Though structured illumination (SI) microscopy is a popular imaging technique conventionally associated with fluorescent super-resolution, recent works have suggested its applicability towards sub-diffraction resolution coherent imaging with quantitative endogenous biological contrast. Here, we demonstrate that SI can efficiently integrate together the principles of fluorescent super-resolution and coherent synthetic aperture to achieve 3D dual-modality sub-diffraction resolution, fluorescence and refractive-index (RI) visualizations of biological samples. We experimentally demonstrate this framework by introducing a SI microscope capable of 3D sub-diffraction resolution fluorescence and RI imaging, and verify its biological visualization capabilities by experimentally reconstructing 3D RI/fluorescence visualizations of fluorescent calibration microspheres as well as alveolar basal epithelial adenocarcinoma (A549) and human colorectal adenocarcinmoa (HT-29) cells, fluorescently stained for F-actin. This demonstration may suggest SI as an especially promising imaging technique to enable future biological studies that explore synergistically operating biophysical/biochemical and molecular mechanisms at sub-diffraction resolutions.
尽管结构光照(SI)显微镜是一种传统上与荧光超分辨率相关的流行成像技术,但最近的研究表明它适用于具有定量内源性生物对比度的亚衍射分辨率相干成像。在这里,我们证明SI可以有效地将荧光超分辨率原理和相干合成孔径原理整合在一起,以实现生物样品的三维双模态亚衍射分辨率、荧光和折射率(RI)可视化。我们通过引入一台能够进行三维亚衍射分辨率荧光和RI成像的SI显微镜,通过实验证明了这个框架,并通过实验重建荧光校准微球以及肺泡基底上皮腺癌(A549)和人结肠腺癌(HT-29)细胞的三维RI/荧光可视化来验证其生物可视化能力,这些细胞用F-肌动蛋白进行了荧光染色。这一演示可能表明SI是一种特别有前途的成像技术,能够推动未来在亚衍射分辨率下协同探索生物物理/生化和分子机制的生物学研究。