Cargando…
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...
Autores principales: | , , , , |
---|---|
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 |
_version_ | 1783477073924325376 |
---|---|
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. |
format | Online Article Text |
id | pubmed-6898998 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT colinyorkhuw distinctactincytoskeletonbehaviourinprimaryandimmortalisedtcells AT kumarisudha distinctactincytoskeletonbehaviourinprimaryandimmortalisedtcells AT barbierililiana distinctactincytoskeletonbehaviourinprimaryandimmortalisedtcells AT cordslena distinctactincytoskeletonbehaviourinprimaryandimmortalisedtcells AT fritzschemarco distinctactincytoskeletonbehaviourinprimaryandimmortalisedtcells |