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Multicolor multiscale brain imaging with chromatic multiphoton serial microscopy

Author

Listed:
  • Lamiae Abdeladim

    (Ecole polytechnique, CNRS, INSERM, IP Paris)

  • Katherine S. Matho

    (Ecole polytechnique, CNRS, INSERM, IP Paris
    CNRS, Institut de la Vision
    Cold Spring Harbor Laboratory)

  • Solène Clavreul

    (CNRS, Institut de la Vision)

  • Pierre Mahou

    (Ecole polytechnique, CNRS, INSERM, IP Paris)

  • Jean-Marc Sintes

    (Ecole polytechnique, CNRS, INSERM, IP Paris)

  • Xavier Solinas

    (Ecole polytechnique, CNRS, INSERM, IP Paris)

  • Ignacio Arganda-Carreras

    (University of the Basque Country
    Basque Foundation for Science
    Donostia International Physics Center (DIPC))

  • Stephen G. Turney

    (Harvard University)

  • Jeff W. Lichtman

    (Harvard University)

  • Anatole Chessel

    (Ecole polytechnique, CNRS, INSERM, IP Paris)

  • Alexis-Pierre Bemelmans

    (Université Paris-Sud)

  • Karine Loulier

    (CNRS, Institut de la Vision)

  • Willy Supatto

    (Ecole polytechnique, CNRS, INSERM, IP Paris)

  • Jean Livet

    (CNRS, Institut de la Vision)

  • Emmanuel Beaurepaire

    (Ecole polytechnique, CNRS, INSERM, IP Paris)

Abstract

Large-scale microscopy approaches are transforming brain imaging, but currently lack efficient multicolor contrast modalities. We introduce chromatic multiphoton serial (ChroMS) microscopy, a method integrating one‐shot multicolor multiphoton excitation through wavelength mixing and serial block-face image acquisition. This approach provides organ-scale micrometric imaging of spectrally distinct fluorescent proteins and label-free nonlinear signals with constant micrometer-scale resolution and sub-micron channel registration over the entire imaged volume. We demonstrate tridimensional (3D) multicolor imaging over several cubic millimeters as well as brain-wide serial 2D multichannel imaging. We illustrate the strengths of this method through color-based 3D analysis of astrocyte morphology and contacts in the mouse cerebral cortex, tracing of individual pyramidal neurons within densely Brainbow-labeled tissue, and multiplexed whole-brain mapping of axonal projections labeled with spectrally distinct tracers. ChroMS will be an asset for multiscale and system-level studies in neuroscience and beyond.

Suggested Citation

  • Lamiae Abdeladim & Katherine S. Matho & Solène Clavreul & Pierre Mahou & Jean-Marc Sintes & Xavier Solinas & Ignacio Arganda-Carreras & Stephen G. Turney & Jeff W. Lichtman & Anatole Chessel & Alexis-, 2019. "Multicolor multiscale brain imaging with chromatic multiphoton serial microscopy," Nature Communications, Nature, vol. 10(1), pages 1-14, December.
  • Handle: RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-09552-9
    DOI: 10.1038/s41467-019-09552-9
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    Cited by:

    1. Wenli Li & Pei He & Dangyuan Lei & Yulong Fan & Yangtao Du & Bo Gao & Zhiqin Chu & Longqiu Li & Kaipeng Liu & Chengxu An & Weizheng Yuan & Yiting Yu, 2023. "Super-resolution multicolor fluorescence microscopy enabled by an apochromatic super-oscillatory lens with extended depth-of-focus," Nature Communications, Nature, vol. 14(1), pages 1-11, December.
    2. Shu Wang & Xiaoxiang Liu & Yueying Li & Xinquan Sun & Qi Li & Yinhua She & Yixuan Xu & Xingxin Huang & Ruolan Lin & Deyong Kang & Xingfu Wang & Haohua Tu & Wenxi Liu & Feng Huang & Jianxin Chen, 2023. "A deep learning-based stripe self-correction method for stitched microscopic images," Nature Communications, Nature, vol. 14(1), pages 1-15, December.

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