Abstract

Optical tomography has emerged as a non-invasive imaging method, providing three-dimensional insights into subcellular structures and thereby enabling a deeper understanding of cellular functions, interactions, and processes. Conventional optical tomography methods are constrained by a limited illumination scanning range, leading to anisotropic resolution and incomplete imaging of cellular structures. To overcome this problem, we employ a compact multi-core fibre-optic cell rotator system that facilitates precise optical manipulation of cells within a microfluidic chip, achieving full-angle projection tomography with isotropic resolution. Moreover, we demonstrate an AI-driven tomographic reconstruction workflow, which can be a paradigm shift from conventional computational methods, often demanding manual processing, to a fully autonomous process. The performance of the proposed cell rotation tomography approach is validated through the three-dimensional reconstruction of cell phantoms and HL60 human cancer cells. The versatility of this learning-based tomographic reconstruction workflow paves the way for its broad application across diverse tomographic imaging modalities, including but not limited to flow cytometry tomography and acoustic rotation tomography. Therefore, this AI-driven approach can propel advancements in cell biology, aiding in the inception of pioneering therapeutics, and augmenting early-stage cancer diagnostics.

Conventional optical tomography can have disadvantages, including anisotropic resolution and incomplete imaging of cellular structures. Here, the authors propose an AI-driven 3D cell imaging system with a cell rotator, which offers improved resolution and automated processing.

Details

Title
AI-driven projection tomography with multicore fibre-optic cell rotation
Author
Sun, Jiawei 1   VIAFID ORCID Logo  ; Yang, Bin 2 ; Koukourakis, Nektarios 3 ; Guck, Jochen 4   VIAFID ORCID Logo  ; Czarske, Juergen W. 5   VIAFID ORCID Logo 

 Shanghai Artificial Intelligence Laboratory, Shanghai, China (GRID:grid.517892.0) (ISNI:0000 0005 0475 7227); TU Dresden, Competence Center for Biomedical Computational Laser Systems (BIOLAS), Dresden, Germany (GRID:grid.4488.0) (ISNI:0000 0001 2111 7257); TU Dresden, Laboratory of Measurement and Sensor System Technique (MST), Dresden, Germany (GRID:grid.4488.0) (ISNI:0000 0001 2111 7257) 
 TU Dresden, Laboratory of Measurement and Sensor System Technique (MST), Dresden, Germany (GRID:grid.4488.0) (ISNI:0000 0001 2111 7257) 
 TU Dresden, Competence Center for Biomedical Computational Laser Systems (BIOLAS), Dresden, Germany (GRID:grid.4488.0) (ISNI:0000 0001 2111 7257); TU Dresden, Laboratory of Measurement and Sensor System Technique (MST), Dresden, Germany (GRID:grid.4488.0) (ISNI:0000 0001 2111 7257) 
 Max Planck Institute for the Science of Light & Max Planck-Zentrum für Physik und Medizin, Erlangen, Germany (GRID:grid.419562.d) (ISNI:0000 0004 0374 4283) 
 TU Dresden, Competence Center for Biomedical Computational Laser Systems (BIOLAS), Dresden, Germany (GRID:grid.4488.0) (ISNI:0000 0001 2111 7257); TU Dresden, Laboratory of Measurement and Sensor System Technique (MST), Dresden, Germany (GRID:grid.4488.0) (ISNI:0000 0001 2111 7257); TU Dresden, Cluster of Excellence Physics of Life, Dresden, Germany (GRID:grid.4488.0) (ISNI:0000 0001 2111 7257); TU Dresden, Institute of Applied Physics, Dresden, Germany (GRID:grid.4488.0) (ISNI:0000 0001 2111 7257) 
Pages
147
Publication year
2024
Publication date
2024
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2909041768
Copyright
© The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.