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Rapid lightsheet fluorescence imaging of whole Drosophila brains at nanoscale resolution by potassium acrylate-based expansion microscopy

Author

Listed:
  • Xuejiao Tian

    (Academia Sinica
    Academia Sinica
    National Tsing Hua University)

  • Tzu-Yang Lin

    (Academia Sinica)

  • Po-Ting Lin

    (Academia Sinica)

  • Min-Ju Tsai

    (Academia Sinica)

  • Hsin Chen

    (Academia Sinica)

  • Wen-Jie Chen

    (National Cheng Kung University and Academia Sinica
    Academia Sinica)

  • Chia-Ming Lee

    (Academia Sinica)

  • Chiao-Hui Tu

    (Academia Sinica)

  • Jui-Cheng Hsu

    (Academia Sinica)

  • Tung-Han Hsieh

    (Academia Sinica)

  • Yi-Chung Tung

    (Academia Sinica)

  • Chien-Kai Wang

    (National Taiwan University)

  • Suewei Lin

    (Academia Sinica)

  • Li-An Chu

    (National Tsing Hua University)

  • Fan-Gang Tseng

    (Academia Sinica
    Academia Sinica
    National Tsing Hua University)

  • Yi-Ping Hsueh

    (Academia Sinica)

  • Chi-Hon Lee

    (Academia Sinica)

  • Peilin Chen

    (Academia Sinica)

  • Bi-Chang Chen

    (Academia Sinica
    Academia Sinica)

Abstract

Taking advantage of the good mechanical strength of expanded Drosophila brains and to tackle their relatively large size that can complicate imaging, we apply potassium (poly)acrylate-based hydrogels for expansion microscopy (ExM), resulting in a 40x plus increased resolution of transgenic fluorescent proteins preserved by glutaraldehyde fixation in the nervous system. Large-volume ExM is realized by using an axicon-based Bessel lightsheet microscope, featuring gentle multi-color fluorophore excitation and intrinsic optical sectioning capability, enabling visualization of Tm5a neurites and L3 lamina neurons with photoreceptors in the optic lobe. We also image nanometer-sized dopaminergic neurons across the same intact iteratively expanded Drosophila brain, enabling us to measure the 3D expansion ratio. Here we show that at a tile scanning speed of ~1 min/mm3 with 1012 pixels over 14 hours, we image the centimeter-sized fly brain at an effective resolution comparable to electron microscopy, allowing us to visualize mitochondria within presynaptic compartments and Bruchpilot (Brp) scaffold proteins distributed in the central complex, enabling robust analyses of neurobiological topics.

Suggested Citation

  • Xuejiao Tian & Tzu-Yang Lin & Po-Ting Lin & Min-Ju Tsai & Hsin Chen & Wen-Jie Chen & Chia-Ming Lee & Chiao-Hui Tu & Jui-Cheng Hsu & Tung-Han Hsieh & Yi-Chung Tung & Chien-Kai Wang & Suewei Lin & Li-An, 2024. "Rapid lightsheet fluorescence imaging of whole Drosophila brains at nanoscale resolution by potassium acrylate-based expansion microscopy," Nature Communications, Nature, vol. 15(1), pages 1-16, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-55305-8
    DOI: 10.1038/s41467-024-55305-8
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