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Decoupling the role of stiffness from other hydroxyapatite signalling cues in periosteal derived stem cell differentiation
Bone extracellular matrix (ECM) is a natural composite made of collagen and mineral hydroxyapatite (HA). Dynamic cell-ECM interactions play a critical role in regulating cell differentiation and function. Understanding the principal ECM cues promoting osteogenic differentiation would be pivotal for...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4451686/ https://www.ncbi.nlm.nih.gov/pubmed/26035412 http://dx.doi.org/10.1038/srep10778 |
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author | Mattei, Giorgio Ferretti, Concetta Tirella, Annalisa Ahluwalia, Arti Mattioli-Belmonte, Monica |
author_facet | Mattei, Giorgio Ferretti, Concetta Tirella, Annalisa Ahluwalia, Arti Mattioli-Belmonte, Monica |
author_sort | Mattei, Giorgio |
collection | PubMed |
description | Bone extracellular matrix (ECM) is a natural composite made of collagen and mineral hydroxyapatite (HA). Dynamic cell-ECM interactions play a critical role in regulating cell differentiation and function. Understanding the principal ECM cues promoting osteogenic differentiation would be pivotal for both bone tissue engineering and regenerative medicine. Altering the mineral content generally modifies the stiffness as well as other physicochemical cues provided by composite materials, complicating the “cause-effect” analysis of resultant cell behaviour. To isolate the contribution of mechanical cues from other HA-derived signals, we developed and characterised composite HA/gelatin scaffolds with different mineral contents along with a set of stiffness-matched HA-free gelatin scaffolds. Samples were seeded with human periosteal derived progenitor cells (PDPCs) and cultured over 7 days, analysing their resultant morphology and gene expression. Our results show that both stiffness and HA contribute to directing PDPC osteogenic differentiation, highlighting the role of stiffness in triggering the expression of osteogenic genes and of HA in accelerating the process, particularly at high concentrations. |
format | Online Article Text |
id | pubmed-4451686 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-44516862015-06-09 Decoupling the role of stiffness from other hydroxyapatite signalling cues in periosteal derived stem cell differentiation Mattei, Giorgio Ferretti, Concetta Tirella, Annalisa Ahluwalia, Arti Mattioli-Belmonte, Monica Sci Rep Article Bone extracellular matrix (ECM) is a natural composite made of collagen and mineral hydroxyapatite (HA). Dynamic cell-ECM interactions play a critical role in regulating cell differentiation and function. Understanding the principal ECM cues promoting osteogenic differentiation would be pivotal for both bone tissue engineering and regenerative medicine. Altering the mineral content generally modifies the stiffness as well as other physicochemical cues provided by composite materials, complicating the “cause-effect” analysis of resultant cell behaviour. To isolate the contribution of mechanical cues from other HA-derived signals, we developed and characterised composite HA/gelatin scaffolds with different mineral contents along with a set of stiffness-matched HA-free gelatin scaffolds. Samples were seeded with human periosteal derived progenitor cells (PDPCs) and cultured over 7 days, analysing their resultant morphology and gene expression. Our results show that both stiffness and HA contribute to directing PDPC osteogenic differentiation, highlighting the role of stiffness in triggering the expression of osteogenic genes and of HA in accelerating the process, particularly at high concentrations. Nature Publishing Group 2015-06-02 /pmc/articles/PMC4451686/ /pubmed/26035412 http://dx.doi.org/10.1038/srep10778 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Mattei, Giorgio Ferretti, Concetta Tirella, Annalisa Ahluwalia, Arti Mattioli-Belmonte, Monica Decoupling the role of stiffness from other hydroxyapatite signalling cues in periosteal derived stem cell differentiation |
title | Decoupling the role of stiffness from other hydroxyapatite signalling cues in periosteal derived stem cell differentiation |
title_full | Decoupling the role of stiffness from other hydroxyapatite signalling cues in periosteal derived stem cell differentiation |
title_fullStr | Decoupling the role of stiffness from other hydroxyapatite signalling cues in periosteal derived stem cell differentiation |
title_full_unstemmed | Decoupling the role of stiffness from other hydroxyapatite signalling cues in periosteal derived stem cell differentiation |
title_short | Decoupling the role of stiffness from other hydroxyapatite signalling cues in periosteal derived stem cell differentiation |
title_sort | decoupling the role of stiffness from other hydroxyapatite signalling cues in periosteal derived stem cell differentiation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4451686/ https://www.ncbi.nlm.nih.gov/pubmed/26035412 http://dx.doi.org/10.1038/srep10778 |
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