Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Arnoldini, Simon, Moscaroli, Alessandra, Chabria, Mamta, Hilbert, Manuel, Hertig, Samuel, Schibli, Roger, Béhé, Martin, Vogel, Viola
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
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
_version_ 1783281559073193984
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
work_keys_str_mv AT arnoldinisimon novelpeptideprobestoassessthetensionalstateoffibronectinfibersincancer
AT moscarolialessandra novelpeptideprobestoassessthetensionalstateoffibronectinfibersincancer
AT chabriamamta novelpeptideprobestoassessthetensionalstateoffibronectinfibersincancer
AT hilbertmanuel novelpeptideprobestoassessthetensionalstateoffibronectinfibersincancer
AT hertigsamuel novelpeptideprobestoassessthetensionalstateoffibronectinfibersincancer
AT schibliroger novelpeptideprobestoassessthetensionalstateoffibronectinfibersincancer
AT behemartin novelpeptideprobestoassessthetensionalstateoffibronectinfibersincancer
AT vogelviola novelpeptideprobestoassessthetensionalstateoffibronectinfibersincancer