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T cell activation requires force generation

Triggering of the T cell receptor (TCR) integrates both binding kinetics and mechanical forces. To understand the contribution of the T cell cytoskeleton to these forces, we triggered T cells using a novel application of atomic force microscopy (AFM). We presented antigenic stimulation using the AFM...

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Detalles Bibliográficos
Autores principales: Hu, Kenneth H., Butte, Manish J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4896056/
https://www.ncbi.nlm.nih.gov/pubmed/27241914
http://dx.doi.org/10.1083/jcb.201511053
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author Hu, Kenneth H.
Butte, Manish J.
author_facet Hu, Kenneth H.
Butte, Manish J.
author_sort Hu, Kenneth H.
collection PubMed
description Triggering of the T cell receptor (TCR) integrates both binding kinetics and mechanical forces. To understand the contribution of the T cell cytoskeleton to these forces, we triggered T cells using a novel application of atomic force microscopy (AFM). We presented antigenic stimulation using the AFM cantilever while simultaneously imaging with optical microscopy and measuring forces on the cantilever. T cells respond forcefully to antigen after calcium flux. All forces and calcium responses were abrogated upon treatment with an F-actin inhibitor. When we emulated the forces of the T cell using the AFM cantilever, even these actin-inhibited T cells became activated. Purely mechanical stimulation was not sufficient; the exogenous forces had to couple through the TCR. These studies suggest a mechanical–chemical feedback loop in which TCR-triggered T cells generate forceful contacts with antigen-presenting cells to improve access to antigen.
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spelling pubmed-48960562016-12-06 T cell activation requires force generation Hu, Kenneth H. Butte, Manish J. J Cell Biol Research Articles Triggering of the T cell receptor (TCR) integrates both binding kinetics and mechanical forces. To understand the contribution of the T cell cytoskeleton to these forces, we triggered T cells using a novel application of atomic force microscopy (AFM). We presented antigenic stimulation using the AFM cantilever while simultaneously imaging with optical microscopy and measuring forces on the cantilever. T cells respond forcefully to antigen after calcium flux. All forces and calcium responses were abrogated upon treatment with an F-actin inhibitor. When we emulated the forces of the T cell using the AFM cantilever, even these actin-inhibited T cells became activated. Purely mechanical stimulation was not sufficient; the exogenous forces had to couple through the TCR. These studies suggest a mechanical–chemical feedback loop in which TCR-triggered T cells generate forceful contacts with antigen-presenting cells to improve access to antigen. The Rockefeller University Press 2016-06-06 /pmc/articles/PMC4896056/ /pubmed/27241914 http://dx.doi.org/10.1083/jcb.201511053 Text en © 2016 Hu and Butte This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Research Articles
Hu, Kenneth H.
Butte, Manish J.
T cell activation requires force generation
title T cell activation requires force generation
title_full T cell activation requires force generation
title_fullStr T cell activation requires force generation
title_full_unstemmed T cell activation requires force generation
title_short T cell activation requires force generation
title_sort t cell activation requires force generation
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4896056/
https://www.ncbi.nlm.nih.gov/pubmed/27241914
http://dx.doi.org/10.1083/jcb.201511053
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