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Cellos: High-throughput deconvolution of 3D organoid dynamics at cellular resolution for cancer pharmacology

Three-dimensional (3D) culture models, such as organoids, are flexible systems to interrogate cellular growth and morphology, multicellular spatial architecture, and cell interactions in response to drug treatment. However, new computational methods to segment and analyze 3D models at cellular resol...

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Autores principales: Mukashyaka, Patience, Kumar, Pooja, Mellert, David J., Nicholas, Shadae, Noorbakhsh, Javad, Brugiolo, Mattia, Anczukow, Olga, Liu, Edison T., Chuang, Jeffrey H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10028797/
https://www.ncbi.nlm.nih.gov/pubmed/36945601
http://dx.doi.org/10.1101/2023.03.03.531019
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author Mukashyaka, Patience
Kumar, Pooja
Mellert, David J.
Nicholas, Shadae
Noorbakhsh, Javad
Brugiolo, Mattia
Anczukow, Olga
Liu, Edison T.
Chuang, Jeffrey H.
author_facet Mukashyaka, Patience
Kumar, Pooja
Mellert, David J.
Nicholas, Shadae
Noorbakhsh, Javad
Brugiolo, Mattia
Anczukow, Olga
Liu, Edison T.
Chuang, Jeffrey H.
author_sort Mukashyaka, Patience
collection PubMed
description Three-dimensional (3D) culture models, such as organoids, are flexible systems to interrogate cellular growth and morphology, multicellular spatial architecture, and cell interactions in response to drug treatment. However, new computational methods to segment and analyze 3D models at cellular resolution with sufficiently high throughput are needed to realize these possibilities. Here we report Cellos (Cell and Organoid Segmentation), an accurate, high throughput image analysis pipeline for 3D organoid and nuclear segmentation analysis. Cellos segments organoids in 3D using classical algorithms and segments nuclei using a Stardist-3D convolutional neural network which we trained on a manually annotated dataset of 3,862 cells from 36 organoids confocally imaged at 5 μm z-resolution. To evaluate the capabilities of Cellos we then analyzed 74,450 organoids with 1.65 million cells, from multiple experiments on triple negative breast cancer organoids containing clonal mixtures with complex cisplatin sensitivities. Cellos was able to accurately distinguish ratios of distinct fluorescently labelled cell populations in organoids, with ≤3% deviation from the seeding ratios in each well and was effective for both fluorescently labelled nuclei and independent DAPI stained datasets. Cellos was able to recapitulate traditional luminescence-based drug response quantifications by analyzing 3D images, including parallel analysis of multiple cancer clones in the same well. Moreover, Cellos was able to identify organoid and nuclear morphology feature changes associated with treatment. Finally, Cellos enables 3D analysis of cell spatial relationships, which we used to detect ecological affinity between cancer cells beyond what arises from local cell division or organoid composition. Cellos provides powerful tools to perform high throughput analysis for pharmacological testing and biological investigation of organoids based on 3D imaging.
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spelling pubmed-100287972023-03-22 Cellos: High-throughput deconvolution of 3D organoid dynamics at cellular resolution for cancer pharmacology Mukashyaka, Patience Kumar, Pooja Mellert, David J. Nicholas, Shadae Noorbakhsh, Javad Brugiolo, Mattia Anczukow, Olga Liu, Edison T. Chuang, Jeffrey H. bioRxiv Article Three-dimensional (3D) culture models, such as organoids, are flexible systems to interrogate cellular growth and morphology, multicellular spatial architecture, and cell interactions in response to drug treatment. However, new computational methods to segment and analyze 3D models at cellular resolution with sufficiently high throughput are needed to realize these possibilities. Here we report Cellos (Cell and Organoid Segmentation), an accurate, high throughput image analysis pipeline for 3D organoid and nuclear segmentation analysis. Cellos segments organoids in 3D using classical algorithms and segments nuclei using a Stardist-3D convolutional neural network which we trained on a manually annotated dataset of 3,862 cells from 36 organoids confocally imaged at 5 μm z-resolution. To evaluate the capabilities of Cellos we then analyzed 74,450 organoids with 1.65 million cells, from multiple experiments on triple negative breast cancer organoids containing clonal mixtures with complex cisplatin sensitivities. Cellos was able to accurately distinguish ratios of distinct fluorescently labelled cell populations in organoids, with ≤3% deviation from the seeding ratios in each well and was effective for both fluorescently labelled nuclei and independent DAPI stained datasets. Cellos was able to recapitulate traditional luminescence-based drug response quantifications by analyzing 3D images, including parallel analysis of multiple cancer clones in the same well. Moreover, Cellos was able to identify organoid and nuclear morphology feature changes associated with treatment. Finally, Cellos enables 3D analysis of cell spatial relationships, which we used to detect ecological affinity between cancer cells beyond what arises from local cell division or organoid composition. Cellos provides powerful tools to perform high throughput analysis for pharmacological testing and biological investigation of organoids based on 3D imaging. Cold Spring Harbor Laboratory 2023-03-06 /pmc/articles/PMC10028797/ /pubmed/36945601 http://dx.doi.org/10.1101/2023.03.03.531019 Text en https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Mukashyaka, Patience
Kumar, Pooja
Mellert, David J.
Nicholas, Shadae
Noorbakhsh, Javad
Brugiolo, Mattia
Anczukow, Olga
Liu, Edison T.
Chuang, Jeffrey H.
Cellos: High-throughput deconvolution of 3D organoid dynamics at cellular resolution for cancer pharmacology
title Cellos: High-throughput deconvolution of 3D organoid dynamics at cellular resolution for cancer pharmacology
title_full Cellos: High-throughput deconvolution of 3D organoid dynamics at cellular resolution for cancer pharmacology
title_fullStr Cellos: High-throughput deconvolution of 3D organoid dynamics at cellular resolution for cancer pharmacology
title_full_unstemmed Cellos: High-throughput deconvolution of 3D organoid dynamics at cellular resolution for cancer pharmacology
title_short Cellos: High-throughput deconvolution of 3D organoid dynamics at cellular resolution for cancer pharmacology
title_sort cellos: high-throughput deconvolution of 3d organoid dynamics at cellular resolution for cancer pharmacology
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10028797/
https://www.ncbi.nlm.nih.gov/pubmed/36945601
http://dx.doi.org/10.1101/2023.03.03.531019
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