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Revealing invisible cell phenotypes with conditional generative modeling

Alexis Lamiable, Tiphaine Champetier, Francesco Leonardi, Ethan Cohen, Peter Sommer, David Hardy, Nicolas Argy, Achille Massougbodji, Elaine Nery, Gilles Cottrell, Yong-Jun Kwon () and Auguste Genovesio ()
Additional contact information
Alexis Lamiable: PSL University
Tiphaine Champetier: PSL University
Francesco Leonardi: PSL University
Ethan Cohen: PSL University
Peter Sommer: Ksilink
David Hardy: Institut Pasteur
Nicolas Argy: Université Paris-Cité, MERIT, IRD
Achille Massougbodji: Institut de Recherche Clinique du Bénin
Elaine Nery: PSL Research University, Department of Translational Research, Cell and Tissue Imaging Facility (PICT-IBiSA)
Gilles Cottrell: Université Paris-Cité, MERIT, IRD
Yong-Jun Kwon: Ksilink
Auguste Genovesio: PSL University

Nature Communications, 2023, vol. 14, issue 1, 1-12

Abstract: Abstract Biological sciences, drug discovery and medicine rely heavily on cell phenotype perturbation and microscope observation. However, most cellular phenotypic changes are subtle and thus hidden from us by natural cell variability: two cells in the same condition already look different. In this study, we show that conditional generative models can be used to transform an image of cells from any one condition to another, thus canceling cell variability. We visually and quantitatively validate that the principle of synthetic cell perturbation works on discernible cases. We then illustrate its effectiveness in displaying otherwise invisible cell phenotypes triggered by blood cells under parasite infection, or by the presence of a disease-causing pathological mutation in differentiated neurons derived from iPSCs, or by low concentration drug treatments. The proposed approach, easy to use and robust, opens the door to more accessible discovery of biological and disease biomarkers.

Date: 2023
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Citations: View citations in EconPapers (2)

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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-42124-6

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DOI: 10.1038/s41467-023-42124-6

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