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Self-supervised classification of subcellular morphometric phenotypes reveals extracellular matrix-specific morphological responses

Cell morphology is profoundly influenced by cellular interactions with microenvironmental factors such as the extracellular matrix (ECM). Upon adhesion to specific ECM, various cell types are known to exhibit different but distinctive morphologies, suggesting that ECM-dependent cell morphological re...

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Autores principales: Wong, Kin Sun, Zhong, Xueying, Low, Christine Siok Lan, Kanchanawong, Pakorn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9468179/
https://www.ncbi.nlm.nih.gov/pubmed/36097150
http://dx.doi.org/10.1038/s41598-022-19472-2
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author Wong, Kin Sun
Zhong, Xueying
Low, Christine Siok Lan
Kanchanawong, Pakorn
author_facet Wong, Kin Sun
Zhong, Xueying
Low, Christine Siok Lan
Kanchanawong, Pakorn
author_sort Wong, Kin Sun
collection PubMed
description Cell morphology is profoundly influenced by cellular interactions with microenvironmental factors such as the extracellular matrix (ECM). Upon adhesion to specific ECM, various cell types are known to exhibit different but distinctive morphologies, suggesting that ECM-dependent cell morphological responses may harbour rich information on cellular signalling states. However, the inherent morphological complexity of cellular and subcellular structures has posed an ongoing challenge for automated quantitative analysis. Since multi-channel fluorescence microscopy provides robust molecular specificity important for the biological interpretations of observed cellular architecture, here we develop a deep learning-based analysis pipeline for the classification of cell morphometric phenotypes from multi-channel fluorescence micrographs, termed SE-RNN (residual neural network with squeeze-and-excite blocks). We demonstrate SERNN-based classification of distinct morphological signatures observed when fibroblasts or epithelial cells are presented with different ECM. Our results underscore how cell shapes are non-random and established the framework for classifying cell shapes into distinct morphological signature in a cell-type and ECM-specific manner.
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spelling pubmed-94681792022-09-14 Self-supervised classification of subcellular morphometric phenotypes reveals extracellular matrix-specific morphological responses Wong, Kin Sun Zhong, Xueying Low, Christine Siok Lan Kanchanawong, Pakorn Sci Rep Article Cell morphology is profoundly influenced by cellular interactions with microenvironmental factors such as the extracellular matrix (ECM). Upon adhesion to specific ECM, various cell types are known to exhibit different but distinctive morphologies, suggesting that ECM-dependent cell morphological responses may harbour rich information on cellular signalling states. However, the inherent morphological complexity of cellular and subcellular structures has posed an ongoing challenge for automated quantitative analysis. Since multi-channel fluorescence microscopy provides robust molecular specificity important for the biological interpretations of observed cellular architecture, here we develop a deep learning-based analysis pipeline for the classification of cell morphometric phenotypes from multi-channel fluorescence micrographs, termed SE-RNN (residual neural network with squeeze-and-excite blocks). We demonstrate SERNN-based classification of distinct morphological signatures observed when fibroblasts or epithelial cells are presented with different ECM. Our results underscore how cell shapes are non-random and established the framework for classifying cell shapes into distinct morphological signature in a cell-type and ECM-specific manner. Nature Publishing Group UK 2022-09-12 /pmc/articles/PMC9468179/ /pubmed/36097150 http://dx.doi.org/10.1038/s41598-022-19472-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Wong, Kin Sun
Zhong, Xueying
Low, Christine Siok Lan
Kanchanawong, Pakorn
Self-supervised classification of subcellular morphometric phenotypes reveals extracellular matrix-specific morphological responses
title Self-supervised classification of subcellular morphometric phenotypes reveals extracellular matrix-specific morphological responses
title_full Self-supervised classification of subcellular morphometric phenotypes reveals extracellular matrix-specific morphological responses
title_fullStr Self-supervised classification of subcellular morphometric phenotypes reveals extracellular matrix-specific morphological responses
title_full_unstemmed Self-supervised classification of subcellular morphometric phenotypes reveals extracellular matrix-specific morphological responses
title_short Self-supervised classification of subcellular morphometric phenotypes reveals extracellular matrix-specific morphological responses
title_sort self-supervised classification of subcellular morphometric phenotypes reveals extracellular matrix-specific morphological responses
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9468179/
https://www.ncbi.nlm.nih.gov/pubmed/36097150
http://dx.doi.org/10.1038/s41598-022-19472-2
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