Evidence map›Paper›PMID 38995963›Full record

ArticlePloS one2024

Virtual tissue microstructure reconstruction across species using generative deep learning.

Nicolás Bettancourt, Cristian Pérez-Gallardo, Valeria Candia, Pamela Guevara, Yannis Kalaidzidis, Marino Zerial, Fabián Segovia-Miranda, Hernán Morales-Navarrete

Abstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Nicolás BettancourtFaculty of Biological Sciences, Department of Cell Biology, Universidad de Concepción, Concepción, Chile.
Cristian Pérez-GallardoFaculty of Biological Sciences, Department of Cell Biology, Universidad de Concepción, Concepción, Chile.
Valeria CandiaFaculty of Biological Sciences, Department of Cell Biology, Universidad de Concepción, Concepción, Chile.
Pamela GuevaraFaculty of Engineering, Department of Electrical Engineering, Universidad de Concepción, Concepción, Chile.ORCID 0000-0001-9988-400X
Yannis KalaidzidisMax Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Marino ZerialMax Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Fabián Segovia-MirandaFaculty of Biological Sciences, Department of Cell Biology, Universidad de Concepción, Concepción, Chile.ORCID 0000-0003-1546-0475
Hernán Morales-NavarreteDepartment of Systems Biology of Development, University of Konstanz, Konstanz, Germany.ORCID 0000-0002-9578-2556

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Analyzing tissue microstructure is essential for understanding complex biological systems in different species. Tissue functions largely depend on their intrinsic tissue architecture. Therefore, studying the three-dimensional (3D) microstructure of tissues, such as the liver, is particularly fascinating due to its conserved essential roles in metabolic processes and detoxification. Here, we present TiMiGNet, a novel deep learning approach for virtual 3D tissue microstructure reconstruction using Generative Adversarial Networks and fluorescence microscopy. TiMiGNet overcomes challenges such as poor antibody penetration and time-intensive procedures by generating accurate, high-resolution predictions of tissue components across large volumes without the need of paired images as input. We applied TiMiGNet to analyze tissue microstructure in mouse and human liver tissue. TiMiGNet shows high performance in predicting structures like bile canaliculi, sinusoids, and Kupffer cell shapes from actin meshwork images. Remarkably, using TiMiGNet we were able to computationally reconstruct tissue structures that cannot be directly imaged due experimental limitations in deep dense tissues, a significant advancement in deep tissue imaging. Our open-source virtual prediction tool facilitates accessible and efficient multi-species tissue microstructure analysis, accommodating researchers with varying expertise levels. Overall, our method represents a powerful approach for studying tissue microstructure, with far-reaching applications in diverse biological contexts and species.

Indexed as

Deep LearningLiverAnimalsHumansImage Processing, Computer-AssistedImaging, Three-DimensionalMiceMicroscopy, Fluorescence

Identifiers

PMID38995963
PMCPMC11244806

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.