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Data driven and cell specific determination of nuclei-associated actin structure
Quantitative and volumetric assessment of filamentous actin fibers (F-actin) remains challenging due to their interconnected nature, leading researchers to utilize threshold based or qualitative measurement methods with poor reproducibility. Here we introduce a novel machine learning based methodolo...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10104112/ https://www.ncbi.nlm.nih.gov/pubmed/37066142 http://dx.doi.org/10.1101/2023.04.06.535937 |
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author | Nikitina, Nina Bursa, Nurbanu Goelzer, Matthew Goldfeldt, Madison Crandall, Chase Howard, Sean Rubin, Janet Satici, Aykut Uzer, Gunes |
author_facet | Nikitina, Nina Bursa, Nurbanu Goelzer, Matthew Goldfeldt, Madison Crandall, Chase Howard, Sean Rubin, Janet Satici, Aykut Uzer, Gunes |
author_sort | Nikitina, Nina |
collection | PubMed |
description | Quantitative and volumetric assessment of filamentous actin fibers (F-actin) remains challenging due to their interconnected nature, leading researchers to utilize threshold based or qualitative measurement methods with poor reproducibility. Here we introduce a novel machine learning based methodology for accurate quantification and reconstruction of nuclei-associated F-actin. Utilizing a Convolutional Neural Network (CNN), we segment actin filaments and nuclei from 3D confocal microscopy images and then reconstruct each fiber by connecting intersecting contours on cross-sectional slices. This allowed measurement of the total number of actin filaments and individual actin filament length and volume in a reproducible fashion. Focusing on the role of F-actin in supporting nucleocytoskeletal connectivity, we quantified apical F-actin, basal F-actin, and nuclear architecture in mesenchymal stem cells (MSCs) following the disruption of the Linker of Nucleoskeleton and Cytoskeleton (LINC) Complexes. Disabling LINC in mesenchymal stem cells (MSCs) generated F-actin disorganization at the nuclear envelope characterized by shorter length and volume of actin fibers contributing a less elongated nuclear shape. Our findings not only present a new tool for mechanobiology but introduce a novel pipeline for developing realistic computational models based on quantitative measures of F-actin. |
format | Online Article Text |
id | pubmed-10104112 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-101041122023-04-15 Data driven and cell specific determination of nuclei-associated actin structure Nikitina, Nina Bursa, Nurbanu Goelzer, Matthew Goldfeldt, Madison Crandall, Chase Howard, Sean Rubin, Janet Satici, Aykut Uzer, Gunes bioRxiv Article Quantitative and volumetric assessment of filamentous actin fibers (F-actin) remains challenging due to their interconnected nature, leading researchers to utilize threshold based or qualitative measurement methods with poor reproducibility. Here we introduce a novel machine learning based methodology for accurate quantification and reconstruction of nuclei-associated F-actin. Utilizing a Convolutional Neural Network (CNN), we segment actin filaments and nuclei from 3D confocal microscopy images and then reconstruct each fiber by connecting intersecting contours on cross-sectional slices. This allowed measurement of the total number of actin filaments and individual actin filament length and volume in a reproducible fashion. Focusing on the role of F-actin in supporting nucleocytoskeletal connectivity, we quantified apical F-actin, basal F-actin, and nuclear architecture in mesenchymal stem cells (MSCs) following the disruption of the Linker of Nucleoskeleton and Cytoskeleton (LINC) Complexes. Disabling LINC in mesenchymal stem cells (MSCs) generated F-actin disorganization at the nuclear envelope characterized by shorter length and volume of actin fibers contributing a less elongated nuclear shape. Our findings not only present a new tool for mechanobiology but introduce a novel pipeline for developing realistic computational models based on quantitative measures of F-actin. Cold Spring Harbor Laboratory 2023-04-06 /pmc/articles/PMC10104112/ /pubmed/37066142 http://dx.doi.org/10.1101/2023.04.06.535937 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Nikitina, Nina Bursa, Nurbanu Goelzer, Matthew Goldfeldt, Madison Crandall, Chase Howard, Sean Rubin, Janet Satici, Aykut Uzer, Gunes Data driven and cell specific determination of nuclei-associated actin structure |
title | Data driven and cell specific determination of nuclei-associated actin structure |
title_full | Data driven and cell specific determination of nuclei-associated actin structure |
title_fullStr | Data driven and cell specific determination of nuclei-associated actin structure |
title_full_unstemmed | Data driven and cell specific determination of nuclei-associated actin structure |
title_short | Data driven and cell specific determination of nuclei-associated actin structure |
title_sort | data driven and cell specific determination of nuclei-associated actin structure |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10104112/ https://www.ncbi.nlm.nih.gov/pubmed/37066142 http://dx.doi.org/10.1101/2023.04.06.535937 |
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