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Adaptive-learning physics-assisted light-field microscopy enables day-long and millisecond-scale super-resolution imaging of 3D subcellular dynamics

Author

Listed:
  • Lanxin Zhu

    (Huazhong University of Science and Technology)

  • Jiahao Sun

    (Huazhong University of Science and Technology)

  • Chengqiang Yi

    (Huazhong University of Science and Technology)

  • Meng Zhang

    (Huazhong University of Science and Technology)

  • Yihang Huang

    (Huazhong University of Science and Technology)

  • Sicen Wu

    (Huazhong University of Science and Technology)

  • Mian He

    (Huazhong University of Science and Technology)

  • Liting Chen

    (Huazhong University of Science and Technology)

  • Yicheng Zhang

    (Huazhong University of Science and Technology)

  • Chunhong Zheng

    (Peking University)

  • Hao Chen

    (Hong Kong University of Science and Technology)

  • Jiang Tang

    (Huazhong University of Science and Technology)

  • Yu-Hui Zhang

    (Huazhong University of Science and Technology)

  • Dongyu Li

    (Huazhong University of Science and Technology
    Huazhong University of Science and Technology)

  • Peng Fei

    (Huazhong University of Science and Technology
    Huazhong University of Science and Technology
    Huazhong University of Science and Technology
    National University of Defense Technology)

Abstract

Long-term and high-spatiotemporal-resolution 3D imaging of living cells remains an unmet challenge for super-resolution microscopy, owing to the noticeable phototoxicity and limited scanning speed. While emerging light-field microscopy can mitigate this issue through three-dimensionally capturing biological dynamics with merely single snapshot, it suffers from suboptimal resolution insufficient for resolving subcellular structures. Here we propose an Adaptive Learning PHysics-Assisted Light-Field Microscopy (Alpha-LFM) with a physics-assisted deep learning framework and adaptive-tuning strategies capable of light-field reconstruction of diverse subcellular dynamics. Alpha-LFM delivers sub-diffraction-limit spatial resolution (up to ~120 nm) while maintaining high temporal resolution and low phototoxicity. It enables rapid and mild 3D super-resolution imaging of diverse intracellular dynamics at hundreds of volumes per second with exceptional details. Using Alpha-LFM approach, we finely resolve the lysosome-mitochondrial interactions, capture rapid motion of peroxisome and the endoplasmic reticulum at 100 volumes per second, and reveal the variations in mitochondrial fission activity throughout two complete cell cycles of 60 h.

Suggested Citation

  • Lanxin Zhu & Jiahao Sun & Chengqiang Yi & Meng Zhang & Yihang Huang & Sicen Wu & Mian He & Liting Chen & Yicheng Zhang & Chunhong Zheng & Hao Chen & Jiang Tang & Yu-Hui Zhang & Dongyu Li & Peng Fei, 2025. "Adaptive-learning physics-assisted light-field microscopy enables day-long and millisecond-scale super-resolution imaging of 3D subcellular dynamics," Nature Communications, Nature, vol. 16(1), pages 1-17, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-62471-w
    DOI: 10.1038/s41467-025-62471-w
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    References listed on IDEAS

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    1. Zhaofei Wang & Jie Wang & Yuxuan Zhao & Jin Jin & Wentian Si & Longbiao Chen & Man Zhang & Yao Zhou & Shiqi Mao & Chunhong Zheng & Yicheng Zhang & Liting Chen & Peng Fei, 2024. "3D live imaging and phenotyping of CAR-T cell mediated-cytotoxicity using high-throughput Bessel oblique plane microscopy," Nature Communications, Nature, vol. 15(1), pages 1-11, December.
    2. Alex M. Valm & Sarah Cohen & Wesley R. Legant & Justin Melunis & Uri Hershberg & Eric Wait & Andrew R. Cohen & Michael W. Davidson & Eric Betzig & Jennifer Lippincott-Schwartz, 2017. "Applying systems-level spectral imaging and analysis to reveal the organelle interactome," Nature, Nature, vol. 546(7656), pages 162-167, June.
    3. Maxime Boutry & Peter K. Kim, 2021. "ORP1L mediated PI(4)P signaling at ER-lysosome-mitochondrion three-way contact contributes to mitochondrial division," Nature Communications, Nature, vol. 12(1), pages 1-18, December.
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