CellINR: Implicitly Overcoming Photo-induced Artifacts in 4D Live Fluorescence Microscopy

πŸ“… 2025-08-25
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In 4D live-cell fluorescence microscopy, prolonged intense illumination induces photobleaching and phototoxicity, introducing artifacts that disrupt structural continuity and impede dynamic quantitative analysis. To address this, we propose CellINRβ€”a novel framework that pioneers the application of implicit neural representations (INRs) to single-sample blind deconvolution optimization. CellINR jointly employs high-frequency spatial mapping and structure-aware enhancement to decouple and reconstruct authentic cellular signals from optical artifacts. We introduce and publicly release the first paired 4D live-cell imaging dataset, enabling rigorous quantitative evaluation. Experiments demonstrate that CellINR significantly outperforms state-of-the-art methods in artifact suppression, 3D structural detail recovery, and temporal coherence across time-lapse sequences. This work establishes a new paradigm for high-fidelity 4D dynamic imaging and facilitates robust downstream biological quantification.

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πŸ“ Abstract
4D live fluorescence microscopy is often compromised by prolonged high intensity illumination which induces photobleaching and phototoxic effects that generate photo-induced artifacts and severely impair image continuity and detail recovery. To address this challenge, we propose the CellINR framework, a case-specific optimization approach based on implicit neural representation. The method employs blind convolution and structure amplification strategies to map 3D spatial coordinates into the high frequency domain, enabling precise modeling and high-accuracy reconstruction of cellular structures while effectively distinguishing true signals from artifacts. Experimental results demonstrate that CellINR significantly outperforms existing techniques in artifact removal and restoration of structural continuity, and for the first time, a paired 4D live cell imaging dataset is provided for evaluating reconstruction performance, thereby offering a solid foundation for subsequent quantitative analyses and biological research. The code and dataset will be public.
Problem

Research questions and friction points this paper is trying to address.

Overcoming photobleaching and phototoxic artifacts
Restoring image continuity in microscopy
Distinguishing true signals from artifacts
Innovation

Methods, ideas, or system contributions that make the work stand out.

Implicit neural representation for artifact removal
Blind convolution and structure amplification strategies
Mapping spatial coordinates to high frequency domain
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