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Molecular Tension Probes to Quantify Cell-Generated Mechanical Forces
Living cells generate, sense, and respond to mechanical forces through their interaction with neighboring cells or extracellular matrix, thereby regulating diverse cellular processes such as growth, motility, differentiation, and immune responses. Dysregulation of mechanosensitive signaling pathways...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Society for Molecular and Cellular Biology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8819489/ https://www.ncbi.nlm.nih.gov/pubmed/35114645 http://dx.doi.org/10.14348/molcells.2022.2049 |
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author | Baek, Kyung Yup Kim, Seohyun Koh, Hye Ran |
author_facet | Baek, Kyung Yup Kim, Seohyun Koh, Hye Ran |
author_sort | Baek, Kyung Yup |
collection | PubMed |
description | Living cells generate, sense, and respond to mechanical forces through their interaction with neighboring cells or extracellular matrix, thereby regulating diverse cellular processes such as growth, motility, differentiation, and immune responses. Dysregulation of mechanosensitive signaling pathways is found associated with the development and progression of various diseases such as cancer. Yet, little is known about the mechanisms behind mechano-regulation, largely due to the limited availability of tools to study it at the molecular level. The recent development of molecular tension probes allows measurement of cellular forces exerted by single ligand-receptor interaction, which has helped in revealing the hitherto unknown mechanistic details of various mechanosensitive processes in living cells. Here, we provide an introductory overview of two methods based on molecular tension probes, tension gauge tether (TGT), and molecular tension fluorescence microscopy (MTFM). TGT utilizes the irreversible rupture of double-stranded DNA tether upon application of force in the piconewton (pN) range, whereas MTFM utilizes the reversible extension of molecular springs such as polymer or single-stranded DNA hairpin under applied pN forces. Specifically, the underlying principle of how molecular tension probes measure cell-generated mechanical forces and their applications to mechanosensitive biological processes are described. |
format | Online Article Text |
id | pubmed-8819489 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Korean Society for Molecular and Cellular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-88194892022-02-15 Molecular Tension Probes to Quantify Cell-Generated Mechanical Forces Baek, Kyung Yup Kim, Seohyun Koh, Hye Ran Mol Cells Minireview Living cells generate, sense, and respond to mechanical forces through their interaction with neighboring cells or extracellular matrix, thereby regulating diverse cellular processes such as growth, motility, differentiation, and immune responses. Dysregulation of mechanosensitive signaling pathways is found associated with the development and progression of various diseases such as cancer. Yet, little is known about the mechanisms behind mechano-regulation, largely due to the limited availability of tools to study it at the molecular level. The recent development of molecular tension probes allows measurement of cellular forces exerted by single ligand-receptor interaction, which has helped in revealing the hitherto unknown mechanistic details of various mechanosensitive processes in living cells. Here, we provide an introductory overview of two methods based on molecular tension probes, tension gauge tether (TGT), and molecular tension fluorescence microscopy (MTFM). TGT utilizes the irreversible rupture of double-stranded DNA tether upon application of force in the piconewton (pN) range, whereas MTFM utilizes the reversible extension of molecular springs such as polymer or single-stranded DNA hairpin under applied pN forces. Specifically, the underlying principle of how molecular tension probes measure cell-generated mechanical forces and their applications to mechanosensitive biological processes are described. Korean Society for Molecular and Cellular Biology 2022-01-31 2022-01-26 /pmc/articles/PMC8819489/ /pubmed/35114645 http://dx.doi.org/10.14348/molcells.2022.2049 Text en © The Korean Society for Molecular and Cellular Biology. All rights reserved. https://creativecommons.org/licenses/by-nc-sa/3.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/ (https://creativecommons.org/licenses/by-nc-sa/3.0/) |
spellingShingle | Minireview Baek, Kyung Yup Kim, Seohyun Koh, Hye Ran Molecular Tension Probes to Quantify Cell-Generated Mechanical Forces |
title | Molecular Tension Probes to Quantify Cell-Generated Mechanical Forces |
title_full | Molecular Tension Probes to Quantify Cell-Generated Mechanical Forces |
title_fullStr | Molecular Tension Probes to Quantify Cell-Generated Mechanical Forces |
title_full_unstemmed | Molecular Tension Probes to Quantify Cell-Generated Mechanical Forces |
title_short | Molecular Tension Probes to Quantify Cell-Generated Mechanical Forces |
title_sort | molecular tension probes to quantify cell-generated mechanical forces |
topic | Minireview |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8819489/ https://www.ncbi.nlm.nih.gov/pubmed/35114645 http://dx.doi.org/10.14348/molcells.2022.2049 |
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