Universal autofocus for quantitative volumetric microscopy of whole mouse brains

被引:37
|
作者
Silvestri, L. [1 ,2 ,3 ]
Mullenbroich, M. C. [2 ,3 ,4 ]
Costantini, I. [2 ,3 ,5 ]
Di Giovanna, A. P. [2 ]
Mazzamuto, G. [2 ,3 ]
Franceschini, A. [2 ]
Kutra, D. [6 ]
Kreshuk, A. [6 ]
Checcucci, C. [2 ,7 ]
Toresano, L. O. [7 ]
Frasconi, P. [7 ]
Sacconi, L. [2 ,3 ]
Pavone, F. S. [1 ,2 ,3 ]
机构
[1] Univ Florence, Dept Phys & Astron, Sesto Fiorentino, Italy
[2] European Lab Nonlinear Spect LENS, Sesto Fiorentino, Italy
[3] CNR, Natl Inst Opt, Sesto Fiorentino, Italy
[4] Univ Glasgow, Sch Phys & Astron, Glasgow, Lanark, Scotland
[5] Univ Florence, Dept Biol, Sesto Fiorentino, Italy
[6] European Mol Biol Lab EMBL, Cell Biol & Biophys Unit, Heidelberg, Germany
[7] Univ Florence, Dept Informat Engn DINFO, Sesto Fiorentino, Italy
基金
欧盟地平线“2020”; 欧洲研究理事会;
关键词
LIGHT-SHEET MICROSCOPY; SEGMENTATION; NEURONS; CELLS;
D O I
10.1038/s41592-021-01208-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
RAPID (rapid autofocusing via pupil-split image phase detection) is a sample-agnostic real-time autofocus method for widefield microscopy. RAPID removes most image degradation in large, cleared samples for enhanced quantitative analyses. Unbiased quantitative analysis of macroscopic biological samples demands fast imaging systems capable of maintaining high resolution across large volumes. Here we introduce RAPID (rapid autofocusing via pupil-split image phase detection), a real-time autofocus method applicable in every widefield-based microscope. RAPID-enabled light-sheet microscopy reliably reconstructs intact, cleared mouse brains with subcellular resolution, and allowed us to characterize the three-dimensional (3D) spatial clustering of somatostatin-positive neurons in the whole encephalon, including densely labeled areas. Furthermore, it enabled 3D morphological analysis of microglia across the entire brain. Beyond light-sheet microscopy, we demonstrate that RAPID maintains high image quality in various settings, from in vivo fluorescence imaging to 3D tracking of fast-moving organisms. RAPID thus provides a flexible autofocus solution that is suitable for traditional automated microscopy tasks as well as for quantitative analysis of large biological specimens.
引用
收藏
页码:953 / +
页数:26
相关论文
共 50 条
  • [41] Microdissection and Whole Mount Scanning Electron Microscopy Visualization of Mouse Choroid Plexus
    Van Wonterghem, Elien
    Van Hoecke, Lien
    Van Imschoot, Griet
    Verhaege, Daan
    Burgelman, Marlies
    Vandenbroucke, Roosmarijn E.
    JOVE-JOURNAL OF VISUALIZED EXPERIMENTS, 2022, (190):
  • [42] Micron-scale Resolution Optical Tomography of Entire Mouse Brains with Confocal Light Sheet Microscopy
    Silvestri, Ludovico
    Bria, Alessandro
    Costantini, Irene
    Sacconi, Leonardo
    Peng, Hanchuan
    Iannello, Giulio
    Pavone, Francesco Saverio
    JOVE-JOURNAL OF VISUALIZED EXPERIMENTS, 2013, (80):
  • [43] Universal Function of Informative-Signal Generation for Quantitative Methods of Scanning Electron Microscopy
    Mikheev N.N.
    Kolesnik A.S.
    Mikheev, N.N. (kmikran@spark-mail.ru), 1600, Izdatel'stvo Nauka (11): : 1265 - 1271
  • [44] FIXATION OF WHOLE MOUSE HEARTS IN SITU FOR ELECTRON MICROSCOPY BY PERFUSION WITH OSMIUM TETROXIDE
    GLACZENS.SS
    THAEMERT, JC
    JOURNAL OF CELL BIOLOGY, 1967, 35 (2P2): : A153 - &
  • [45] Morphological study of embryonic Chd8+/− mouse brains using light-sheet microscopy
    Harold F. Gómez
    Leonie Hodel
    Odyssé Michos
    Dagmar Iber
    BMC Research Notes, 14
  • [46] Imaging volumetric dynamics at high speed in mouse and zebrafish brain with confocal light field microscopy
    Zhenkun Zhang
    Lu Bai
    Lin Cong
    Peng Yu
    Tianlei Zhang
    Wanzhuo Shi
    Funing Li
    Jiulin Du
    Kai Wang
    Nature Biotechnology, 2021, 39 : 74 - 83
  • [47] Imaging volumetric dynamics at high speed in mouse and zebrafish brain with confocal light field microscopy
    Zhang, Zhenkun
    Bai, Lu
    Cong, Lin
    Yu, Peng
    Zhang, Tianlei
    Shi, Wanzhuo
    Li, Funing
    Du, Jiulin
    Wang, Kai
    NATURE BIOTECHNOLOGY, 2021, 39 (01) : 74 - 83
  • [48] Volumetric voltage imaging of neuronal populations in the mouse brain by confocal light-field microscopy
    Bai, Lu
    Cong, Lin
    Shi, Ziqi
    Zhao, Yuchen
    Zhang, Yujie
    Lu, Bin
    Zhang, Jing
    Xiong, Zhi-Qi
    Xu, Ninglong
    Mu, Yu
    Wang, Kai
    NATURE METHODS, 2024, 21 (11) : 2160 - 2170
  • [49] Confocal Laser Scanning Microscopy-Based Quantitative Analysis of Aspergillus fumigatus Conidia Distribution in Whole-Mount Optically Cleared Mouse Lung
    Maslov, Ivan, V
    Bogorodskiy, Andrey O.
    Pavelchenko, Mariia, V
    Zykov, Ilia O.
    Troyanova, Natalya, I
    Borshchevskiy, Valentin, I
    Shevchenko, Marina A.
    JOVE-JOURNAL OF VISUALIZED EXPERIMENTS, 2021, (175):
  • [50] NEW METHOD FOR QUANTITATIVE MEASUREMENT OF N-NITROSODIMETHYLAMINE FORMATION IN THE WHOLE MOUSE
    KAWANISHI, T
    TAKAHASHI, A
    OHNO, Y
    TAKANAKA, A
    KASUYA, Y
    OMORI, Y
    ARCHIVES OF TOXICOLOGY, 1983, 54 (04) : 323 - 330