Revealing invisible cell phenotypes with conditional generative modeling

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...

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Published inNature communications Vol. 14; no. 1; p. 6386
Main Authors Lamiable, Alexis, Champetier, Tiphaine, Leonardi, Francesco, Cohen, Ethan, Sommer, Peter, Hardy, David, Argy, Nicolas, Massougbodji, Achille, Del Nery, Elaine, Cottrell, Gilles, Kwon, Yong-Jun, Genovesio, Auguste
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 11.10.2023
Nature Publishing Group
Nature Portfolio
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Summary: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. Biological research relies on observing cell phenotypes, often obscured by natural variability. Here, the authors use generative modelling to unveil hidden changes triggered by infections, mutations, or drugs, allowing for accessible discovery of biomarkers.
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PMCID: PMC10567685
ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-023-42124-6