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RAD-TGTs: high-throughput measurement of cellular mechanotype via rupture and delivery of DNA tension probes

Mechanical forces drive critical cellular processes that are reflected in mechanical phenotypes, or mechanotypes, of cells and their microenvironment. We present here “Rupture And Deliver” Tension Gauge Tethers (RAD-TGTs) in which flow cytometry is used to record the mechanical history of thousands...

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Autores principales: Pawlak, Matthew R., Smiley, Adam T., Ramirez, Maria Paz, Kelly, Marcus D., Shamsan, Ghaidan A., Anderson, Sarah M., Smeester, Branden A., Largaespada, David A., Odde, David J., Gordon, Wendy R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10147940/
https://www.ncbi.nlm.nih.gov/pubmed/37117218
http://dx.doi.org/10.1038/s41467-023-38157-6
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author Pawlak, Matthew R.
Smiley, Adam T.
Ramirez, Maria Paz
Kelly, Marcus D.
Shamsan, Ghaidan A.
Anderson, Sarah M.
Smeester, Branden A.
Largaespada, David A.
Odde, David J.
Gordon, Wendy R.
author_facet Pawlak, Matthew R.
Smiley, Adam T.
Ramirez, Maria Paz
Kelly, Marcus D.
Shamsan, Ghaidan A.
Anderson, Sarah M.
Smeester, Branden A.
Largaespada, David A.
Odde, David J.
Gordon, Wendy R.
author_sort Pawlak, Matthew R.
collection PubMed
description Mechanical forces drive critical cellular processes that are reflected in mechanical phenotypes, or mechanotypes, of cells and their microenvironment. We present here “Rupture And Deliver” Tension Gauge Tethers (RAD-TGTs) in which flow cytometry is used to record the mechanical history of thousands of cells exerting forces on their surroundings via their propensity to rupture immobilized DNA duplex tension probes. We demonstrate that RAD-TGTs recapitulate prior DNA tension probe studies while also yielding a gain of fluorescence in the force-generating cell that is detectable by flow cytometry. Furthermore, the rupture propensity is altered following disruption of the cytoskeleton using drugs or CRISPR-knockout of mechanosensing proteins. Importantly, RAD-TGTs can differentiate distinct mechanotypes among mixed populations of cells. We also establish oligo rupture and delivery can be measured via DNA sequencing. RAD-TGTs provide a facile and powerful assay to enable high-throughput mechanotype profiling, which could find various applications, for example, in combination with CRISPR screens and -omics analysis.
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spelling pubmed-101479402023-04-30 RAD-TGTs: high-throughput measurement of cellular mechanotype via rupture and delivery of DNA tension probes Pawlak, Matthew R. Smiley, Adam T. Ramirez, Maria Paz Kelly, Marcus D. Shamsan, Ghaidan A. Anderson, Sarah M. Smeester, Branden A. Largaespada, David A. Odde, David J. Gordon, Wendy R. Nat Commun Article Mechanical forces drive critical cellular processes that are reflected in mechanical phenotypes, or mechanotypes, of cells and their microenvironment. We present here “Rupture And Deliver” Tension Gauge Tethers (RAD-TGTs) in which flow cytometry is used to record the mechanical history of thousands of cells exerting forces on their surroundings via their propensity to rupture immobilized DNA duplex tension probes. We demonstrate that RAD-TGTs recapitulate prior DNA tension probe studies while also yielding a gain of fluorescence in the force-generating cell that is detectable by flow cytometry. Furthermore, the rupture propensity is altered following disruption of the cytoskeleton using drugs or CRISPR-knockout of mechanosensing proteins. Importantly, RAD-TGTs can differentiate distinct mechanotypes among mixed populations of cells. We also establish oligo rupture and delivery can be measured via DNA sequencing. RAD-TGTs provide a facile and powerful assay to enable high-throughput mechanotype profiling, which could find various applications, for example, in combination with CRISPR screens and -omics analysis. Nature Publishing Group UK 2023-04-28 /pmc/articles/PMC10147940/ /pubmed/37117218 http://dx.doi.org/10.1038/s41467-023-38157-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Pawlak, Matthew R.
Smiley, Adam T.
Ramirez, Maria Paz
Kelly, Marcus D.
Shamsan, Ghaidan A.
Anderson, Sarah M.
Smeester, Branden A.
Largaespada, David A.
Odde, David J.
Gordon, Wendy R.
RAD-TGTs: high-throughput measurement of cellular mechanotype via rupture and delivery of DNA tension probes
title RAD-TGTs: high-throughput measurement of cellular mechanotype via rupture and delivery of DNA tension probes
title_full RAD-TGTs: high-throughput measurement of cellular mechanotype via rupture and delivery of DNA tension probes
title_fullStr RAD-TGTs: high-throughput measurement of cellular mechanotype via rupture and delivery of DNA tension probes
title_full_unstemmed RAD-TGTs: high-throughput measurement of cellular mechanotype via rupture and delivery of DNA tension probes
title_short RAD-TGTs: high-throughput measurement of cellular mechanotype via rupture and delivery of DNA tension probes
title_sort rad-tgts: high-throughput measurement of cellular mechanotype via rupture and delivery of dna tension probes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10147940/
https://www.ncbi.nlm.nih.gov/pubmed/37117218
http://dx.doi.org/10.1038/s41467-023-38157-6
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