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Super-Resolution Imaging Approaches for Quantifying F-Actin in Immune Cells

Immune cells comprise a diverse set of cells that undergo a complex array of biological processes that must be tightly regulated. A key component of cellular machinery that achieves this is the cytoskeleton. Therefore, imaging and quantitatively describing the architecture and dynamics of the cytosk...

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Detalles Bibliográficos
Autores principales: Garlick, Evelyn, Thomas, Steven G., Owen, Dylan M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8416680/
https://www.ncbi.nlm.nih.gov/pubmed/34490240
http://dx.doi.org/10.3389/fcell.2021.676066
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author Garlick, Evelyn
Thomas, Steven G.
Owen, Dylan M.
author_facet Garlick, Evelyn
Thomas, Steven G.
Owen, Dylan M.
author_sort Garlick, Evelyn
collection PubMed
description Immune cells comprise a diverse set of cells that undergo a complex array of biological processes that must be tightly regulated. A key component of cellular machinery that achieves this is the cytoskeleton. Therefore, imaging and quantitatively describing the architecture and dynamics of the cytoskeleton is an important research goal. Optical microscopy is well suited to this task. Here, we review the latest in the state-of-the-art methodology for labeling the cytoskeleton, fluorescence microscopy hardware suitable for such imaging and quantitative statistical analysis software applicable to describing cytoskeletal structures. We also highlight ongoing challenges and areas for future development.
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spelling pubmed-84166802021-09-05 Super-Resolution Imaging Approaches for Quantifying F-Actin in Immune Cells Garlick, Evelyn Thomas, Steven G. Owen, Dylan M. Front Cell Dev Biol Cell and Developmental Biology Immune cells comprise a diverse set of cells that undergo a complex array of biological processes that must be tightly regulated. A key component of cellular machinery that achieves this is the cytoskeleton. Therefore, imaging and quantitatively describing the architecture and dynamics of the cytoskeleton is an important research goal. Optical microscopy is well suited to this task. Here, we review the latest in the state-of-the-art methodology for labeling the cytoskeleton, fluorescence microscopy hardware suitable for such imaging and quantitative statistical analysis software applicable to describing cytoskeletal structures. We also highlight ongoing challenges and areas for future development. Frontiers Media S.A. 2021-08-19 /pmc/articles/PMC8416680/ /pubmed/34490240 http://dx.doi.org/10.3389/fcell.2021.676066 Text en Copyright © 2021 Garlick, Thomas and Owen. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Garlick, Evelyn
Thomas, Steven G.
Owen, Dylan M.
Super-Resolution Imaging Approaches for Quantifying F-Actin in Immune Cells
title Super-Resolution Imaging Approaches for Quantifying F-Actin in Immune Cells
title_full Super-Resolution Imaging Approaches for Quantifying F-Actin in Immune Cells
title_fullStr Super-Resolution Imaging Approaches for Quantifying F-Actin in Immune Cells
title_full_unstemmed Super-Resolution Imaging Approaches for Quantifying F-Actin in Immune Cells
title_short Super-Resolution Imaging Approaches for Quantifying F-Actin in Immune Cells
title_sort super-resolution imaging approaches for quantifying f-actin in immune cells
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8416680/
https://www.ncbi.nlm.nih.gov/pubmed/34490240
http://dx.doi.org/10.3389/fcell.2021.676066
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