Virtual tissue microstructure reconstruction across species using generative deep learning

PLoS One. 2024 Jul 12;19(7):e0306073. doi: 10.1371/journal.pone.0306073. eCollection 2024.

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.

MeSH terms

  • Animals
  • Deep Learning*
  • Humans
  • Image Processing, Computer-Assisted / methods
  • Imaging, Three-Dimensional / methods
  • Liver*
  • Mice
  • Microscopy, Fluorescence / methods

Grants and funding

This work was financially supported by Fondo Nacional de Desarrollo Científico y Tecnológico, ANID Fondecyt regular 1200965 to FS-M, VRID-UdeC 2024001079INV to FS-M, and ANID-Basal Center FB210017 (CENIA) to PG. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.