Cargando…
Microparticle traction force microscopy reveals subcellular force exertion patterns in immune cell–target interactions
Force exertion is an integral part of cellular behavior. Traction force microscopy (TFM) has been instrumental for studying such forces, providing spatial force measurements at subcellular resolution. However, the applications of classical TFM are restricted by the typical planar geometry. Here, we...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6946705/ https://www.ncbi.nlm.nih.gov/pubmed/31911639 http://dx.doi.org/10.1038/s41467-019-13804-z |
_version_ | 1783485417922756608 |
---|---|
author | Vorselen, Daan Wang, Yifan de Jesus, Miguel M. Shah, Pavak K. Footer, Matthew J. Huse, Morgan Cai, Wei Theriot, Julie A. |
author_facet | Vorselen, Daan Wang, Yifan de Jesus, Miguel M. Shah, Pavak K. Footer, Matthew J. Huse, Morgan Cai, Wei Theriot, Julie A. |
author_sort | Vorselen, Daan |
collection | PubMed |
description | Force exertion is an integral part of cellular behavior. Traction force microscopy (TFM) has been instrumental for studying such forces, providing spatial force measurements at subcellular resolution. However, the applications of classical TFM are restricted by the typical planar geometry. Here, we develop a particle-based force sensing strategy for studying cellular interactions. We establish a straightforward batch approach for synthesizing uniform, deformable and tuneable hydrogel particles, which can also be easily derivatized. The 3D shape of such particles can be resolved with superresolution (<50 nm) accuracy using conventional confocal microscopy. We introduce a reference-free computational method allowing inference of traction forces with high sensitivity directly from the particle shape. We illustrate the potential of this approach by revealing subcellular force patterns throughout phagocytic engulfment and force dynamics in the cytotoxic T-cell immunological synapse. This strategy can readily be adapted for studying cellular forces in a wide range of applications. |
format | Online Article Text |
id | pubmed-6946705 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69467052020-01-09 Microparticle traction force microscopy reveals subcellular force exertion patterns in immune cell–target interactions Vorselen, Daan Wang, Yifan de Jesus, Miguel M. Shah, Pavak K. Footer, Matthew J. Huse, Morgan Cai, Wei Theriot, Julie A. Nat Commun Article Force exertion is an integral part of cellular behavior. Traction force microscopy (TFM) has been instrumental for studying such forces, providing spatial force measurements at subcellular resolution. However, the applications of classical TFM are restricted by the typical planar geometry. Here, we develop a particle-based force sensing strategy for studying cellular interactions. We establish a straightforward batch approach for synthesizing uniform, deformable and tuneable hydrogel particles, which can also be easily derivatized. The 3D shape of such particles can be resolved with superresolution (<50 nm) accuracy using conventional confocal microscopy. We introduce a reference-free computational method allowing inference of traction forces with high sensitivity directly from the particle shape. We illustrate the potential of this approach by revealing subcellular force patterns throughout phagocytic engulfment and force dynamics in the cytotoxic T-cell immunological synapse. This strategy can readily be adapted for studying cellular forces in a wide range of applications. Nature Publishing Group UK 2020-01-07 /pmc/articles/PMC6946705/ /pubmed/31911639 http://dx.doi.org/10.1038/s41467-019-13804-z Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Vorselen, Daan Wang, Yifan de Jesus, Miguel M. Shah, Pavak K. Footer, Matthew J. Huse, Morgan Cai, Wei Theriot, Julie A. Microparticle traction force microscopy reveals subcellular force exertion patterns in immune cell–target interactions |
title | Microparticle traction force microscopy reveals subcellular force exertion patterns in immune cell–target interactions |
title_full | Microparticle traction force microscopy reveals subcellular force exertion patterns in immune cell–target interactions |
title_fullStr | Microparticle traction force microscopy reveals subcellular force exertion patterns in immune cell–target interactions |
title_full_unstemmed | Microparticle traction force microscopy reveals subcellular force exertion patterns in immune cell–target interactions |
title_short | Microparticle traction force microscopy reveals subcellular force exertion patterns in immune cell–target interactions |
title_sort | microparticle traction force microscopy reveals subcellular force exertion patterns in immune cell–target interactions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6946705/ https://www.ncbi.nlm.nih.gov/pubmed/31911639 http://dx.doi.org/10.1038/s41467-019-13804-z |
work_keys_str_mv | AT vorselendaan microparticletractionforcemicroscopyrevealssubcellularforceexertionpatternsinimmunecelltargetinteractions AT wangyifan microparticletractionforcemicroscopyrevealssubcellularforceexertionpatternsinimmunecelltargetinteractions AT dejesusmiguelm microparticletractionforcemicroscopyrevealssubcellularforceexertionpatternsinimmunecelltargetinteractions AT shahpavakk microparticletractionforcemicroscopyrevealssubcellularforceexertionpatternsinimmunecelltargetinteractions AT footermatthewj microparticletractionforcemicroscopyrevealssubcellularforceexertionpatternsinimmunecelltargetinteractions AT husemorgan microparticletractionforcemicroscopyrevealssubcellularforceexertionpatternsinimmunecelltargetinteractions AT caiwei microparticletractionforcemicroscopyrevealssubcellularforceexertionpatternsinimmunecelltargetinteractions AT theriotjuliea microparticletractionforcemicroscopyrevealssubcellularforceexertionpatternsinimmunecelltargetinteractions |