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Novel peptide probes to assess the tensional state of fibronectin fibers in cancer
Transformations of extracellular matrix (ECM) accompany pathological tissue changes, yet how cell-ECM crosstalk drives these processes remains unknown as adequate tools to probe forces or mechanical strains in tissues are lacking. Here, we introduce a new nanoprobe to assess the mechanical strain of...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5702617/ https://www.ncbi.nlm.nih.gov/pubmed/29176724 http://dx.doi.org/10.1038/s41467-017-01846-0 |
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author | Arnoldini, Simon Moscaroli, Alessandra Chabria, Mamta Hilbert, Manuel Hertig, Samuel Schibli, Roger Béhé, Martin Vogel, Viola |
author_facet | Arnoldini, Simon Moscaroli, Alessandra Chabria, Mamta Hilbert, Manuel Hertig, Samuel Schibli, Roger Béhé, Martin Vogel, Viola |
author_sort | Arnoldini, Simon |
collection | PubMed |
description | Transformations of extracellular matrix (ECM) accompany pathological tissue changes, yet how cell-ECM crosstalk drives these processes remains unknown as adequate tools to probe forces or mechanical strains in tissues are lacking. Here, we introduce a new nanoprobe to assess the mechanical strain of fibronectin (Fn) fibers in tissue, based on the bacterial Fn-binding peptide FnBPA5. FnBPA5 exhibits nM binding affinity to relaxed, but not stretched Fn fibers and is shown to exhibit strain-sensitive ECM binding in cell culture in a comparison with an established Fn-FRET probe. Staining of tumor tissue cryosections shows large regions of relaxed Fn fibers and injection of radiolabeled (111)In-FnBPA5 in a prostate cancer mouse model reveals specific accumulation of (111)In-FnBPA5 in tumor with prolonged retention compared to other organs. The herein presented approach enables to investigate how Fn fiber strain at the tissue level impacts cell signaling and pathological progression in different diseases. |
format | Online Article Text |
id | pubmed-5702617 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57026172017-11-29 Novel peptide probes to assess the tensional state of fibronectin fibers in cancer Arnoldini, Simon Moscaroli, Alessandra Chabria, Mamta Hilbert, Manuel Hertig, Samuel Schibli, Roger Béhé, Martin Vogel, Viola Nat Commun Article Transformations of extracellular matrix (ECM) accompany pathological tissue changes, yet how cell-ECM crosstalk drives these processes remains unknown as adequate tools to probe forces or mechanical strains in tissues are lacking. Here, we introduce a new nanoprobe to assess the mechanical strain of fibronectin (Fn) fibers in tissue, based on the bacterial Fn-binding peptide FnBPA5. FnBPA5 exhibits nM binding affinity to relaxed, but not stretched Fn fibers and is shown to exhibit strain-sensitive ECM binding in cell culture in a comparison with an established Fn-FRET probe. Staining of tumor tissue cryosections shows large regions of relaxed Fn fibers and injection of radiolabeled (111)In-FnBPA5 in a prostate cancer mouse model reveals specific accumulation of (111)In-FnBPA5 in tumor with prolonged retention compared to other organs. The herein presented approach enables to investigate how Fn fiber strain at the tissue level impacts cell signaling and pathological progression in different diseases. Nature Publishing Group UK 2017-11-27 /pmc/articles/PMC5702617/ /pubmed/29176724 http://dx.doi.org/10.1038/s41467-017-01846-0 Text en © The Author(s) 2017 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 Commonslicense, unless indicated otherwise in a credit line to the material. If material is not included in the article’sCreative 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 Arnoldini, Simon Moscaroli, Alessandra Chabria, Mamta Hilbert, Manuel Hertig, Samuel Schibli, Roger Béhé, Martin Vogel, Viola Novel peptide probes to assess the tensional state of fibronectin fibers in cancer |
title | Novel peptide probes to assess the tensional state of fibronectin fibers in cancer |
title_full | Novel peptide probes to assess the tensional state of fibronectin fibers in cancer |
title_fullStr | Novel peptide probes to assess the tensional state of fibronectin fibers in cancer |
title_full_unstemmed | Novel peptide probes to assess the tensional state of fibronectin fibers in cancer |
title_short | Novel peptide probes to assess the tensional state of fibronectin fibers in cancer |
title_sort | novel peptide probes to assess the tensional state of fibronectin fibers in cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5702617/ https://www.ncbi.nlm.nih.gov/pubmed/29176724 http://dx.doi.org/10.1038/s41467-017-01846-0 |
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