High-throughput widefield fluorescence imaging of 3D samples using deep learning for 2D projection image restoration.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2022
Historique:
received: 03 02 2022
accepted: 05 05 2022
entrez: 19 5 2022
pubmed: 20 5 2022
medline: 24 5 2022
Statut: epublish

Résumé

Fluorescence microscopy is a core method for visualizing and quantifying the spatial and temporal dynamics of complex biological processes. While many fluorescent microscopy techniques exist, due to its cost-effectiveness and accessibility, widefield fluorescent imaging remains one of the most widely used. To accomplish imaging of 3D samples, conventional widefield fluorescence imaging entails acquiring a sequence of 2D images spaced along the z-dimension, typically called a z-stack. Oftentimes, the first step in an analysis pipeline is to project that 3D volume into a single 2D image because 3D image data can be cumbersome to manage and challenging to analyze and interpret. Furthermore, z-stack acquisition is often time-consuming, which consequently may induce photodamage to the biological sample; these are major barriers for workflows that require high-throughput, such as drug screening. As an alternative to z-stacks, axial sweep acquisition schemes have been proposed to circumvent these drawbacks and offer potential of 100-fold faster image acquisition for 3D-samples compared to z-stack acquisition. Unfortunately, these acquisition techniques generate low-quality 2D z-projected images that require restoration with unwieldy, computationally heavy algorithms before the images can be interrogated. We propose a novel workflow to combine axial z-sweep acquisition with deep learning-based image restoration, ultimately enabling high-throughput and high-quality imaging of complex 3D-samples using 2D projection images. To demonstrate the capabilities of our proposed workflow, we apply it to live-cell imaging of large 3D tumor spheroid cultures and find we can produce high-fidelity images appropriate for quantitative analysis. Therefore, we conclude that combining axial z-sweep image acquisition with deep learning-based image restoration enables high-throughput and high-quality fluorescence imaging of complex 3D biological samples.

Identifiants

pubmed: 35588399
doi: 10.1371/journal.pone.0264241
pii: PONE-D-22-03425
pmc: PMC9119453
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0264241

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Références

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Auteurs

Edvin Forsgren (E)

Computational Life Science Cluster (CLiC), Department of Chemistry, Umeå University, Umeå, Sweden.

Christoffer Edlund (C)

Sartorius Corporate Research, Sartorius Stedim Data Analytics AB, Umeå, Sweden.

Miniver Oliver (M)

Sartorius BioAnalytics, Essen BioScience, Ltd., Units 2 & 3 The Quadrant, Royston, Hertfordshire, United Kingdom.

Kalpana Barnes (K)

Sartorius BioAnalytics, Essen BioScience, Ltd., Units 2 & 3 The Quadrant, Royston, Hertfordshire, United Kingdom.

Rickard Sjögren (R)

Sartorius Corporate Research, Sartorius Stedim Data Analytics AB, Umeå, Sweden.

Timothy R Jackson (TR)

Sartorius BioAnalytics, Essen BioScience, Ltd., Units 2 & 3 The Quadrant, Royston, Hertfordshire, United Kingdom.

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