3DCellPol: joint detection and pairing of cell structures to compute cell polarity

Bibliographic Details
Main Author: Narotamo, Hemaxi
Publication Date: 2025
Other Authors: Franco, Cláudio A., Silveira, Margarida
Format: Article
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: http://hdl.handle.net/10400.14/48040
Summary: Cell polarity is essential for tissue structure and cell migration, and its dysregulation is linked to diseases such as cancer and vascular disorders. Understanding the associations between molecular mechanisms, such as genetic defects, and abnormal cell polarization can provide clinicians with valuable biomarkers for early disease diagnosis and lead to more targeted therapeutic interventions. Here, we present a deep-learning framework for cell polarity computation based on the association between pairs of objects. Our approach, named 3DCellPol, is trained to detect and group the centroids of two distinct objects. To demonstrate the potential of 3DCellPol, we use it to compute cell polarity by pairing two cell organelles: nuclei and Golgi. The vectors between nuclei and Golgi define the front-rear polarity axis in endothelial cells. 3DCellPol was evaluated on 3D microscopy images of mouse retinas. It detected 71% of the nucleus–Golgi vectors and outperformed previous methods while requiring much less supervision. Moreover, incorporating synthetic data generated by a generative adversarial network further improved detection to 78%. We additionally demonstrated our model's adaptability to 2D images by applying it to a public dataset of cervical cytology images, where polarity is defined based on the cytoplasm-nucleus vectors. In this dataset, our model detected over 90% of vectors. 3DCellPol's ability to robustly compute cell polarity is crucial for understanding mechanisms of diseases where abnormal polarity plays a key role, and it may contribute to improved diagnostics and enable targeted therapies. Hence, it is a valuable open-source tool for both biomedical research and clinical practice.
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spelling 3DCellPol: joint detection and pairing of cell structures to compute cell polarity3D fluorescence microscopy imagesCell polarity vectorsDeep learningEndothelial cell front-rear polarityGenerative adversarial networksCell polarity is essential for tissue structure and cell migration, and its dysregulation is linked to diseases such as cancer and vascular disorders. Understanding the associations between molecular mechanisms, such as genetic defects, and abnormal cell polarization can provide clinicians with valuable biomarkers for early disease diagnosis and lead to more targeted therapeutic interventions. Here, we present a deep-learning framework for cell polarity computation based on the association between pairs of objects. Our approach, named 3DCellPol, is trained to detect and group the centroids of two distinct objects. To demonstrate the potential of 3DCellPol, we use it to compute cell polarity by pairing two cell organelles: nuclei and Golgi. The vectors between nuclei and Golgi define the front-rear polarity axis in endothelial cells. 3DCellPol was evaluated on 3D microscopy images of mouse retinas. It detected 71% of the nucleus–Golgi vectors and outperformed previous methods while requiring much less supervision. Moreover, incorporating synthetic data generated by a generative adversarial network further improved detection to 78%. We additionally demonstrated our model's adaptability to 2D images by applying it to a public dataset of cervical cytology images, where polarity is defined based on the cytoplasm-nucleus vectors. In this dataset, our model detected over 90% of vectors. 3DCellPol's ability to robustly compute cell polarity is crucial for understanding mechanisms of diseases where abnormal polarity plays a key role, and it may contribute to improved diagnostics and enable targeted therapies. Hence, it is a valuable open-source tool for both biomedical research and clinical practice.VeritatiNarotamo, HemaxiFranco, Cláudio A.Silveira, Margarida2025-02-04T12:08:56Z2025-062025-06-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.14/48040eng1746-809410.1016/j.bspc.2025.107537info:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2025-03-13T15:10:43Zoai:repositorio.ucp.pt:10400.14/48040Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-29T02:10:39.318929Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv 3DCellPol: joint detection and pairing of cell structures to compute cell polarity
title 3DCellPol: joint detection and pairing of cell structures to compute cell polarity
spellingShingle 3DCellPol: joint detection and pairing of cell structures to compute cell polarity
Narotamo, Hemaxi
3D fluorescence microscopy images
Cell polarity vectors
Deep learning
Endothelial cell front-rear polarity
Generative adversarial networks
title_short 3DCellPol: joint detection and pairing of cell structures to compute cell polarity
title_full 3DCellPol: joint detection and pairing of cell structures to compute cell polarity
title_fullStr 3DCellPol: joint detection and pairing of cell structures to compute cell polarity
title_full_unstemmed 3DCellPol: joint detection and pairing of cell structures to compute cell polarity
title_sort 3DCellPol: joint detection and pairing of cell structures to compute cell polarity
author Narotamo, Hemaxi
author_facet Narotamo, Hemaxi
Franco, Cláudio A.
Silveira, Margarida
author_role author
author2 Franco, Cláudio A.
Silveira, Margarida
author2_role author
author
dc.contributor.none.fl_str_mv Veritati
dc.contributor.author.fl_str_mv Narotamo, Hemaxi
Franco, Cláudio A.
Silveira, Margarida
dc.subject.por.fl_str_mv 3D fluorescence microscopy images
Cell polarity vectors
Deep learning
Endothelial cell front-rear polarity
Generative adversarial networks
topic 3D fluorescence microscopy images
Cell polarity vectors
Deep learning
Endothelial cell front-rear polarity
Generative adversarial networks
description Cell polarity is essential for tissue structure and cell migration, and its dysregulation is linked to diseases such as cancer and vascular disorders. Understanding the associations between molecular mechanisms, such as genetic defects, and abnormal cell polarization can provide clinicians with valuable biomarkers for early disease diagnosis and lead to more targeted therapeutic interventions. Here, we present a deep-learning framework for cell polarity computation based on the association between pairs of objects. Our approach, named 3DCellPol, is trained to detect and group the centroids of two distinct objects. To demonstrate the potential of 3DCellPol, we use it to compute cell polarity by pairing two cell organelles: nuclei and Golgi. The vectors between nuclei and Golgi define the front-rear polarity axis in endothelial cells. 3DCellPol was evaluated on 3D microscopy images of mouse retinas. It detected 71% of the nucleus–Golgi vectors and outperformed previous methods while requiring much less supervision. Moreover, incorporating synthetic data generated by a generative adversarial network further improved detection to 78%. We additionally demonstrated our model's adaptability to 2D images by applying it to a public dataset of cervical cytology images, where polarity is defined based on the cytoplasm-nucleus vectors. In this dataset, our model detected over 90% of vectors. 3DCellPol's ability to robustly compute cell polarity is crucial for understanding mechanisms of diseases where abnormal polarity plays a key role, and it may contribute to improved diagnostics and enable targeted therapies. Hence, it is a valuable open-source tool for both biomedical research and clinical practice.
publishDate 2025
dc.date.none.fl_str_mv 2025-02-04T12:08:56Z
2025-06
2025-06-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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format article
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dc.language.iso.fl_str_mv eng
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dc.relation.none.fl_str_mv 1746-8094
10.1016/j.bspc.2025.107537
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