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Morphological profiling by high-throughput single-cell biophysical fractometry
Complex and irregular cell architecture is known to statistically exhibit fractal geometry, i.e., a pattern resembles a smaller part of itself. Although fractal variations in cells are proven to be closely associated with the disease-related phenotypes that are otherwise obscured in the standard cel...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10126163/ https://www.ncbi.nlm.nih.gov/pubmed/37095203 http://dx.doi.org/10.1038/s42003-023-04839-6 |
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author | Zhang, Ziqi Lee, Kelvin C. M. Siu, Dickson M. D. Lo, Michelle C. K. Lai, Queenie T. K. Lam, Edmund Y. Tsia, Kevin K. |
author_facet | Zhang, Ziqi Lee, Kelvin C. M. Siu, Dickson M. D. Lo, Michelle C. K. Lai, Queenie T. K. Lam, Edmund Y. Tsia, Kevin K. |
author_sort | Zhang, Ziqi |
collection | PubMed |
description | Complex and irregular cell architecture is known to statistically exhibit fractal geometry, i.e., a pattern resembles a smaller part of itself. Although fractal variations in cells are proven to be closely associated with the disease-related phenotypes that are otherwise obscured in the standard cell-based assays, fractal analysis with single-cell precision remains largely unexplored. To close this gap, here we develop an image-based approach that quantifies a multitude of single-cell biophysical fractal-related properties at subcellular resolution. Taking together with its high-throughput single-cell imaging performance (~10,000 cells/sec), this technique, termed single-cell biophysical fractometry, offers sufficient statistical power for delineating the cellular heterogeneity, in the context of lung-cancer cell subtype classification, drug response assays and cell-cycle progression tracking. Further correlative fractal analysis shows that single-cell biophysical fractometry can enrich the standard morphological profiling depth and spearhead systematic fractal analysis of how cell morphology encodes cellular health and pathological conditions. |
format | Online Article Text |
id | pubmed-10126163 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-101261632023-04-26 Morphological profiling by high-throughput single-cell biophysical fractometry Zhang, Ziqi Lee, Kelvin C. M. Siu, Dickson M. D. Lo, Michelle C. K. Lai, Queenie T. K. Lam, Edmund Y. Tsia, Kevin K. Commun Biol Article Complex and irregular cell architecture is known to statistically exhibit fractal geometry, i.e., a pattern resembles a smaller part of itself. Although fractal variations in cells are proven to be closely associated with the disease-related phenotypes that are otherwise obscured in the standard cell-based assays, fractal analysis with single-cell precision remains largely unexplored. To close this gap, here we develop an image-based approach that quantifies a multitude of single-cell biophysical fractal-related properties at subcellular resolution. Taking together with its high-throughput single-cell imaging performance (~10,000 cells/sec), this technique, termed single-cell biophysical fractometry, offers sufficient statistical power for delineating the cellular heterogeneity, in the context of lung-cancer cell subtype classification, drug response assays and cell-cycle progression tracking. Further correlative fractal analysis shows that single-cell biophysical fractometry can enrich the standard morphological profiling depth and spearhead systematic fractal analysis of how cell morphology encodes cellular health and pathological conditions. Nature Publishing Group UK 2023-04-24 /pmc/articles/PMC10126163/ /pubmed/37095203 http://dx.doi.org/10.1038/s42003-023-04839-6 Text en © The Author(s) 2023 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Zhang, Ziqi Lee, Kelvin C. M. Siu, Dickson M. D. Lo, Michelle C. K. Lai, Queenie T. K. Lam, Edmund Y. Tsia, Kevin K. Morphological profiling by high-throughput single-cell biophysical fractometry |
title | Morphological profiling by high-throughput single-cell biophysical fractometry |
title_full | Morphological profiling by high-throughput single-cell biophysical fractometry |
title_fullStr | Morphological profiling by high-throughput single-cell biophysical fractometry |
title_full_unstemmed | Morphological profiling by high-throughput single-cell biophysical fractometry |
title_short | Morphological profiling by high-throughput single-cell biophysical fractometry |
title_sort | morphological profiling by high-throughput single-cell biophysical fractometry |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10126163/ https://www.ncbi.nlm.nih.gov/pubmed/37095203 http://dx.doi.org/10.1038/s42003-023-04839-6 |
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