Light-field deep learning enables high-throughput, scattering-mitigated calcium imaging

Light-field microscopy (LFM) enables high-throughput functional imaging by scanlessly encoding entire volumes in single snapshots. However, LFM's computational burden and vulnerability to scattering limit its application to biological imaging. We present a light-field strategy for volumetric, scattering-mitigated neural circuit activity monitoring. A physics-based deep neural network, 2PiLnet, is trained with two-photon volumes and one-photon light fields. Light-field videos of jGCaMP8f-expressing neurons are acquired in neocortical brain slices. 2PiLnet reconstructs volumes with two-photon-like contrast and source confinement from scattered, blurry one-photon light fields from fields-of-view for which no two-photon images are provided. This enables automated segmentation and extraction of calcium signals with high signal-to-noise ratios and reduces optical crosstalk compared to conventional volume reconstruction methods. Imaging 100 volumes per second, we observe putative spikes fired at up to 10 Hz and the spatial intermingling of putative ensembles throughout [Formula: see text]-micron volumes. Compared to iterative algorithms, 2PiLnet workflows reduce light-field video processing times by several-fold, advancing the goal of real-time, scattering-robust volumetric neural circuit imaging for closed-loop and adaptive experimental paradigms.

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Publication Details

Journal
Proceedings of the National Academy of Sciences
Published
2025-11-25
DOI
https://doi.org/10.1073/pnas.2510337122
Primary Topic
Advanced Fluorescence Microscopy Techniques
Type
article
Field-Weighted Citation Impact
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article

Light-field deep learning enables high-throughput, scattering-mitigated calcium imaging

Amanda J. Foust, Samuel J. Barnes, Pier Luigi Dragotti, Carmel L. Howe et al.
Proceedings of the National Academy of Sciences
Advanced Fluorescence Microscopy Techniques
article

Light-field deep learning enables high-throughput, scattering-mitigated calcium imaging

Amanda J. Foust, Samuel J. Barnes, Pier Luigi Dragotti, Carmel L. Howe, Pingfan Song, Herman Verinaz-Jadan, K. Y. Zhao
article en

Abstract

Light-field microscopy (LFM) enables high-throughput functional imaging by scanlessly encoding entire volumes in single snapshots. However, LFM's computational burden and vulnerability to scattering limit its application to biological imaging. We present a light-field strategy for volumetric, scattering-mitigated neural circuit activity monitoring. A physics-based deep neural network, 2PiLnet, is trained with two-photon volumes and one-photon light fields. Light-field videos of jGCaMP8f-expressing neurons are acquired in neocortical brain slices. 2PiLnet reconstructs volumes with two-photon-like contrast and source confinement from scattered, blurry one-photon light fields from fields-of-view for which no two-photon images are provided. This enables automated segmentation and extraction of calcium signals with high signal-to-noise ratios and reduces optical crosstalk compared to conventional volume reconstruction methods. Imaging 100 volumes per second, we observe putative spikes fired at up to 10 Hz and the spatial intermingling of putative ensembles throughout [Formula: see text]-micron volumes. Compared to iterative algorithms, 2PiLnet workflows reduce light-field video processing times by several-fold, advancing the goal of real-time, scattering-robust volumetric neural circuit imaging for closed-loop and adaptive experimental paradigms.

Proceedings of the National Academy of SciencesVol. 122(48)
Escuela Superior Politecnica del Litoral (EC), University of Cambridge (GB), Hammersmith Hospital (GB), Faculty (United Kingdom) (GB), UK Dementia Research Institute (GB), Institute of Information Engineering (CN), Imperial College London (GB)
Openalex Percentile: Top 75%
Advanced Fluorescence Microscopy Techniques
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