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Distinct actin cytoskeleton behaviour in primary and immortalised T-cells

Cytoskeletal actin dynamics are crucial for the activation of T-cells. Immortalised Jurkat T-cells have been the model system of choice to examine and correlate the dynamics of the actin cytoskeleton and the immunological synapse leading to T-cell activation. However, it has remained unclear whether...

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Autores principales: Colin-York, Huw, Kumari, Sudha, Barbieri, Liliana, Cords, Lena, Fritzsche, Marco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6898998/
https://www.ncbi.nlm.nih.gov/pubmed/31413071
http://dx.doi.org/10.1242/jcs.232322
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author Colin-York, Huw
Kumari, Sudha
Barbieri, Liliana
Cords, Lena
Fritzsche, Marco
author_facet Colin-York, Huw
Kumari, Sudha
Barbieri, Liliana
Cords, Lena
Fritzsche, Marco
author_sort Colin-York, Huw
collection PubMed
description Cytoskeletal actin dynamics are crucial for the activation of T-cells. Immortalised Jurkat T-cells have been the model system of choice to examine and correlate the dynamics of the actin cytoskeleton and the immunological synapse leading to T-cell activation. However, it has remained unclear whether immortalised cellular systems, such as Jurkat T-cells can recapitulate the cytoskeletal behaviour of primary T-cells. Studies delineating the cytoskeletal behaviour of Jurkat T-cells in comparison to primary T-cells are lacking. Here, we employ live-cell super-resolution microscopy to investigate the cytoskeletal actin organisation and dynamics of living primary and immortalised Jurkat T-cells at the appropriate spatiotemporal resolution. Under comparable activation conditions, we found differences in the architectural organisation and dynamics of Jurkat and primary mouse and human T-cells. Although the three main actin network architectures in Jurkat T-cells were reminiscent of primary T-cells, there were differences in the organisation and molecular mechanisms underlying these networks. Our results highlight mechanistic distinctions in the T-cell model system most utilised to study cytoskeletal actin dynamics.
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spelling pubmed-68989982019-12-10 Distinct actin cytoskeleton behaviour in primary and immortalised T-cells Colin-York, Huw Kumari, Sudha Barbieri, Liliana Cords, Lena Fritzsche, Marco J Cell Sci Short Report Cytoskeletal actin dynamics are crucial for the activation of T-cells. Immortalised Jurkat T-cells have been the model system of choice to examine and correlate the dynamics of the actin cytoskeleton and the immunological synapse leading to T-cell activation. However, it has remained unclear whether immortalised cellular systems, such as Jurkat T-cells can recapitulate the cytoskeletal behaviour of primary T-cells. Studies delineating the cytoskeletal behaviour of Jurkat T-cells in comparison to primary T-cells are lacking. Here, we employ live-cell super-resolution microscopy to investigate the cytoskeletal actin organisation and dynamics of living primary and immortalised Jurkat T-cells at the appropriate spatiotemporal resolution. Under comparable activation conditions, we found differences in the architectural organisation and dynamics of Jurkat and primary mouse and human T-cells. Although the three main actin network architectures in Jurkat T-cells were reminiscent of primary T-cells, there were differences in the organisation and molecular mechanisms underlying these networks. Our results highlight mechanistic distinctions in the T-cell model system most utilised to study cytoskeletal actin dynamics. The Company of Biologists Ltd 2019-09-04 /pmc/articles/PMC6898998/ /pubmed/31413071 http://dx.doi.org/10.1242/jcs.232322 Text en © 2019. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/4.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Short Report
Colin-York, Huw
Kumari, Sudha
Barbieri, Liliana
Cords, Lena
Fritzsche, Marco
Distinct actin cytoskeleton behaviour in primary and immortalised T-cells
title Distinct actin cytoskeleton behaviour in primary and immortalised T-cells
title_full Distinct actin cytoskeleton behaviour in primary and immortalised T-cells
title_fullStr Distinct actin cytoskeleton behaviour in primary and immortalised T-cells
title_full_unstemmed Distinct actin cytoskeleton behaviour in primary and immortalised T-cells
title_short Distinct actin cytoskeleton behaviour in primary and immortalised T-cells
title_sort distinct actin cytoskeleton behaviour in primary and immortalised t-cells
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6898998/
https://www.ncbi.nlm.nih.gov/pubmed/31413071
http://dx.doi.org/10.1242/jcs.232322
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