Cargando…
N-Cadherin adhesive interactions modulate matrix mechanosensing and fate commitment of mesenchymal stem cells
During mesenchymal development, the microenvironment gradually transitions from one that is rich in cell-cell interactions to one that is dominated by cell-extracellular-matrix (ECM) interactions. Because these cues cannot readily be decoupled in vitro or in vivo, how they converge to regulate mesen...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5121068/ https://www.ncbi.nlm.nih.gov/pubmed/27525568 http://dx.doi.org/10.1038/nmat4725 |
_version_ | 1782469339285291008 |
---|---|
author | Cosgrove, Brian D. Mui, Keeley L. Driscoll, Tristan P. Caliari, Steven R. Mehta, Kush D. Assoian, Richard K. Burdick, Jason A. Mauck, Robert L. |
author_facet | Cosgrove, Brian D. Mui, Keeley L. Driscoll, Tristan P. Caliari, Steven R. Mehta, Kush D. Assoian, Richard K. Burdick, Jason A. Mauck, Robert L. |
author_sort | Cosgrove, Brian D. |
collection | PubMed |
description | During mesenchymal development, the microenvironment gradually transitions from one that is rich in cell-cell interactions to one that is dominated by cell-extracellular-matrix (ECM) interactions. Because these cues cannot readily be decoupled in vitro or in vivo, how they converge to regulate mesenchymal stem cell (MSC) mechanosensing is not fully understood. Here, we show that a hyaluronic acid hydrogel system enables, across a physiological range of ECM stiffness, the independent co-presentation of the HAVDI adhesive motif from the EC1 domain of N-Cadherin and the RGD adhesive motif from fibronectin. Decoupled presentation of these cues revealed that HAVDI ligation (at constant RGD ligation) reduced the contractile state and thereby nuclear YAP/TAZ localization in MSCs, resulting in altered interpretation of ECM stiffness and subsequent changes in downstream cell proliferation and differentiation. Our findings reveal that, in an evolving developmental context, HAVDI/N-Cadherin interactions can alter stem cell perception of the stiffening extracellular microenvironment. |
format | Online Article Text |
id | pubmed-5121068 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
record_format | MEDLINE/PubMed |
spelling | pubmed-51210682017-02-15 N-Cadherin adhesive interactions modulate matrix mechanosensing and fate commitment of mesenchymal stem cells Cosgrove, Brian D. Mui, Keeley L. Driscoll, Tristan P. Caliari, Steven R. Mehta, Kush D. Assoian, Richard K. Burdick, Jason A. Mauck, Robert L. Nat Mater Article During mesenchymal development, the microenvironment gradually transitions from one that is rich in cell-cell interactions to one that is dominated by cell-extracellular-matrix (ECM) interactions. Because these cues cannot readily be decoupled in vitro or in vivo, how they converge to regulate mesenchymal stem cell (MSC) mechanosensing is not fully understood. Here, we show that a hyaluronic acid hydrogel system enables, across a physiological range of ECM stiffness, the independent co-presentation of the HAVDI adhesive motif from the EC1 domain of N-Cadherin and the RGD adhesive motif from fibronectin. Decoupled presentation of these cues revealed that HAVDI ligation (at constant RGD ligation) reduced the contractile state and thereby nuclear YAP/TAZ localization in MSCs, resulting in altered interpretation of ECM stiffness and subsequent changes in downstream cell proliferation and differentiation. Our findings reveal that, in an evolving developmental context, HAVDI/N-Cadherin interactions can alter stem cell perception of the stiffening extracellular microenvironment. 2016-08-15 2016-12 /pmc/articles/PMC5121068/ /pubmed/27525568 http://dx.doi.org/10.1038/nmat4725 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Cosgrove, Brian D. Mui, Keeley L. Driscoll, Tristan P. Caliari, Steven R. Mehta, Kush D. Assoian, Richard K. Burdick, Jason A. Mauck, Robert L. N-Cadherin adhesive interactions modulate matrix mechanosensing and fate commitment of mesenchymal stem cells |
title | N-Cadherin adhesive interactions modulate matrix mechanosensing and fate commitment of mesenchymal stem cells |
title_full | N-Cadherin adhesive interactions modulate matrix mechanosensing and fate commitment of mesenchymal stem cells |
title_fullStr | N-Cadherin adhesive interactions modulate matrix mechanosensing and fate commitment of mesenchymal stem cells |
title_full_unstemmed | N-Cadherin adhesive interactions modulate matrix mechanosensing and fate commitment of mesenchymal stem cells |
title_short | N-Cadherin adhesive interactions modulate matrix mechanosensing and fate commitment of mesenchymal stem cells |
title_sort | n-cadherin adhesive interactions modulate matrix mechanosensing and fate commitment of mesenchymal stem cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5121068/ https://www.ncbi.nlm.nih.gov/pubmed/27525568 http://dx.doi.org/10.1038/nmat4725 |
work_keys_str_mv | AT cosgrovebriand ncadherinadhesiveinteractionsmodulatematrixmechanosensingandfatecommitmentofmesenchymalstemcells AT muikeeleyl ncadherinadhesiveinteractionsmodulatematrixmechanosensingandfatecommitmentofmesenchymalstemcells AT driscolltristanp ncadherinadhesiveinteractionsmodulatematrixmechanosensingandfatecommitmentofmesenchymalstemcells AT caliaristevenr ncadherinadhesiveinteractionsmodulatematrixmechanosensingandfatecommitmentofmesenchymalstemcells AT mehtakushd ncadherinadhesiveinteractionsmodulatematrixmechanosensingandfatecommitmentofmesenchymalstemcells AT assoianrichardk ncadherinadhesiveinteractionsmodulatematrixmechanosensingandfatecommitmentofmesenchymalstemcells AT burdickjasona ncadherinadhesiveinteractionsmodulatematrixmechanosensingandfatecommitmentofmesenchymalstemcells AT mauckrobertl ncadherinadhesiveinteractionsmodulatematrixmechanosensingandfatecommitmentofmesenchymalstemcells |