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Visualizing Cellular Dynamics and Protein Localization in 3D Collagen

Immune cells migrate and communicate through cell-to-cell interactions and cytokines to coordinate the specificity and timing of the immune response. While studying these events in cell culture are standard procedure, spatiotemporal dynamics of cell-to-cell interactions within three-dimensional (3D)...

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Detalles Bibliográficos
Autores principales: Koh, Wan Hon, Zayats, Romaniya, Lopez, Paul, Murooka, Thomas T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7757667/
https://www.ncbi.nlm.nih.gov/pubmed/33377097
http://dx.doi.org/10.1016/j.xpro.2020.100203
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author Koh, Wan Hon
Zayats, Romaniya
Lopez, Paul
Murooka, Thomas T.
author_facet Koh, Wan Hon
Zayats, Romaniya
Lopez, Paul
Murooka, Thomas T.
author_sort Koh, Wan Hon
collection PubMed
description Immune cells migrate and communicate through cell-to-cell interactions and cytokines to coordinate the specificity and timing of the immune response. While studying these events in cell culture are standard procedure, spatiotemporal dynamics of cell-to-cell interactions within three-dimensional (3D) environments are critical in generating appropriate effector functions. Here, we present a detailed protocol to study cells within an all-in-one 3D collagen matrix that is amenable to live-cell microscopy and immunohistochemistry. This approach facilitates analyses of dynamic cellular events in 3D settings. For complete details on the use and execution of this protocol, please refer to Koh et al. (2020).
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spelling pubmed-77576672020-12-28 Visualizing Cellular Dynamics and Protein Localization in 3D Collagen Koh, Wan Hon Zayats, Romaniya Lopez, Paul Murooka, Thomas T. STAR Protoc Protocol Immune cells migrate and communicate through cell-to-cell interactions and cytokines to coordinate the specificity and timing of the immune response. While studying these events in cell culture are standard procedure, spatiotemporal dynamics of cell-to-cell interactions within three-dimensional (3D) environments are critical in generating appropriate effector functions. Here, we present a detailed protocol to study cells within an all-in-one 3D collagen matrix that is amenable to live-cell microscopy and immunohistochemistry. This approach facilitates analyses of dynamic cellular events in 3D settings. For complete details on the use and execution of this protocol, please refer to Koh et al. (2020). Elsevier 2020-12-08 /pmc/articles/PMC7757667/ /pubmed/33377097 http://dx.doi.org/10.1016/j.xpro.2020.100203 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Protocol
Koh, Wan Hon
Zayats, Romaniya
Lopez, Paul
Murooka, Thomas T.
Visualizing Cellular Dynamics and Protein Localization in 3D Collagen
title Visualizing Cellular Dynamics and Protein Localization in 3D Collagen
title_full Visualizing Cellular Dynamics and Protein Localization in 3D Collagen
title_fullStr Visualizing Cellular Dynamics and Protein Localization in 3D Collagen
title_full_unstemmed Visualizing Cellular Dynamics and Protein Localization in 3D Collagen
title_short Visualizing Cellular Dynamics and Protein Localization in 3D Collagen
title_sort visualizing cellular dynamics and protein localization in 3d collagen
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7757667/
https://www.ncbi.nlm.nih.gov/pubmed/33377097
http://dx.doi.org/10.1016/j.xpro.2020.100203
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