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Spatial heterogeneity of the cytosol revealed by machine learning-based 3D particle tracking
The spatial structure and physical properties of the cytosol are not well understood. Measurements of the material state of the cytosol are challenging due to its spatial and temporal heterogeneity. Recent development of genetically encoded multimeric nanoparticles (GEMs) has opened up study of the...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7359570/ https://www.ncbi.nlm.nih.gov/pubmed/32401664 http://dx.doi.org/10.1091/mbc.E20-03-0210 |
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author | McLaughlin, Grace A. Langdon, Erin M. Crutchley, John M. Holt, Liam J. Forest, M. Gregory Newby, Jay M. Gladfelter, Amy S. |
author_facet | McLaughlin, Grace A. Langdon, Erin M. Crutchley, John M. Holt, Liam J. Forest, M. Gregory Newby, Jay M. Gladfelter, Amy S. |
author_sort | McLaughlin, Grace A. |
collection | PubMed |
description | The spatial structure and physical properties of the cytosol are not well understood. Measurements of the material state of the cytosol are challenging due to its spatial and temporal heterogeneity. Recent development of genetically encoded multimeric nanoparticles (GEMs) has opened up study of the cytosol at the length scales of multiprotein complexes (20–60 nm). We developed an image analysis pipeline for 3D imaging of GEMs in the context of large, multinucleate fungi where there is evidence of functional compartmentalization of the cytosol for both the nuclear division cycle and branching. We applied a neural network to track particles in 3D and then created quantitative visualizations of spatially varying diffusivity. Using this pipeline to analyze spatial diffusivity patterns, we found that there is substantial variability in the properties of the cytosol. We detected zones where GEMs display especially low diffusivity at hyphal tips and near some nuclei, showing that the physical state of the cytosol varies spatially within a single cell. Additionally, we observed significant cell-to-cell variability in the average diffusivity of GEMs. Thus, the physical properties of the cytosol vary substantially in time and space and can be a source of heterogeneity within individual cells and across populations. |
format | Online Article Text |
id | pubmed-7359570 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-73595702020-09-16 Spatial heterogeneity of the cytosol revealed by machine learning-based 3D particle tracking McLaughlin, Grace A. Langdon, Erin M. Crutchley, John M. Holt, Liam J. Forest, M. Gregory Newby, Jay M. Gladfelter, Amy S. Mol Biol Cell Articles The spatial structure and physical properties of the cytosol are not well understood. Measurements of the material state of the cytosol are challenging due to its spatial and temporal heterogeneity. Recent development of genetically encoded multimeric nanoparticles (GEMs) has opened up study of the cytosol at the length scales of multiprotein complexes (20–60 nm). We developed an image analysis pipeline for 3D imaging of GEMs in the context of large, multinucleate fungi where there is evidence of functional compartmentalization of the cytosol for both the nuclear division cycle and branching. We applied a neural network to track particles in 3D and then created quantitative visualizations of spatially varying diffusivity. Using this pipeline to analyze spatial diffusivity patterns, we found that there is substantial variability in the properties of the cytosol. We detected zones where GEMs display especially low diffusivity at hyphal tips and near some nuclei, showing that the physical state of the cytosol varies spatially within a single cell. Additionally, we observed significant cell-to-cell variability in the average diffusivity of GEMs. Thus, the physical properties of the cytosol vary substantially in time and space and can be a source of heterogeneity within individual cells and across populations. The American Society for Cell Biology 2020-07-01 /pmc/articles/PMC7359570/ /pubmed/32401664 http://dx.doi.org/10.1091/mbc.E20-03-0210 Text en © 2020 McLaughlin et al. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. http://creativecommons.org/licenses/by-nc-sa/3.0 This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License. |
spellingShingle | Articles McLaughlin, Grace A. Langdon, Erin M. Crutchley, John M. Holt, Liam J. Forest, M. Gregory Newby, Jay M. Gladfelter, Amy S. Spatial heterogeneity of the cytosol revealed by machine learning-based 3D particle tracking |
title | Spatial heterogeneity of the cytosol revealed by machine learning-based 3D particle tracking |
title_full | Spatial heterogeneity of the cytosol revealed by machine learning-based 3D particle tracking |
title_fullStr | Spatial heterogeneity of the cytosol revealed by machine learning-based 3D particle tracking |
title_full_unstemmed | Spatial heterogeneity of the cytosol revealed by machine learning-based 3D particle tracking |
title_short | Spatial heterogeneity of the cytosol revealed by machine learning-based 3D particle tracking |
title_sort | spatial heterogeneity of the cytosol revealed by machine learning-based 3d particle tracking |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7359570/ https://www.ncbi.nlm.nih.gov/pubmed/32401664 http://dx.doi.org/10.1091/mbc.E20-03-0210 |
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