Human osteoblasts within soft peptide hydrogels promote mineralisation in vitro

Biomaterials that provide three-dimensional support networks for the culture of cells are being developed for a wide range of tissue engineering applications including the regeneration of bone. This study explores the potential of the versatile ionic-complementary peptide, FEFEFKFK, for such a purpo...

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Main Authors: Luis A Castillo Diaz, Alberto Saiani, Julie E Gough, Aline F Miller
Format: Article
Language:English
Published: SAGE Publishing 2014-07-01
Series:Journal of Tissue Engineering
Online Access:https://doi.org/10.1177/2041731414539344
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spelling doaj-53b41dfe924a4a159676f6094d29f8922020-11-25T02:50:41ZengSAGE PublishingJournal of Tissue Engineering2041-73142014-07-01510.1177/204173141453934410.1177_2041731414539344Human osteoblasts within soft peptide hydrogels promote mineralisation in vitroLuis A Castillo Diaz0Alberto Saiani1Julie E Gough2Aline F Miller3Manchester Institute of Biotechnology, The University of Manchester, Manchester, UKSchool of Materials, The University of Manchester, Manchester, UKSchool of Materials, The University of Manchester, Manchester, UKManchester Institute of Biotechnology, The University of Manchester, Manchester, UKBiomaterials that provide three-dimensional support networks for the culture of cells are being developed for a wide range of tissue engineering applications including the regeneration of bone. This study explores the potential of the versatile ionic-complementary peptide, FEFEFKFK, for such a purpose as this peptide spontaneously self-assembles into β-sheet-rich fibres that subsequently self-associate to form self-supporting hydrogels. Via simple live/dead cell assays, we demonstrated that 3 wt% hydrogels were optimal for the support of osteoblast cells. We went on to show that these cells are not only viable within the three-dimensional hydrogel but they also proliferate and produce osteogenic key proteins, that is, they behave like in vivo bone cells, over the 14-day period explored here. The gel elasticity increased over time when cells were present – in comparison to a decrease in control samples – indicating the deposition of matrix throughout the peptide scaffold. Moreover, significant quantities of calcium phosphate were deposited. Collectively, these data demonstrate that ionic-complementary octapeptides offer a suitable three-dimensional environment for osteoblastic cell function.https://doi.org/10.1177/2041731414539344
collection DOAJ
language English
format Article
sources DOAJ
author Luis A Castillo Diaz
Alberto Saiani
Julie E Gough
Aline F Miller
spellingShingle Luis A Castillo Diaz
Alberto Saiani
Julie E Gough
Aline F Miller
Human osteoblasts within soft peptide hydrogels promote mineralisation in vitro
Journal of Tissue Engineering
author_facet Luis A Castillo Diaz
Alberto Saiani
Julie E Gough
Aline F Miller
author_sort Luis A Castillo Diaz
title Human osteoblasts within soft peptide hydrogels promote mineralisation in vitro
title_short Human osteoblasts within soft peptide hydrogels promote mineralisation in vitro
title_full Human osteoblasts within soft peptide hydrogels promote mineralisation in vitro
title_fullStr Human osteoblasts within soft peptide hydrogels promote mineralisation in vitro
title_full_unstemmed Human osteoblasts within soft peptide hydrogels promote mineralisation in vitro
title_sort human osteoblasts within soft peptide hydrogels promote mineralisation in vitro
publisher SAGE Publishing
series Journal of Tissue Engineering
issn 2041-7314
publishDate 2014-07-01
description Biomaterials that provide three-dimensional support networks for the culture of cells are being developed for a wide range of tissue engineering applications including the regeneration of bone. This study explores the potential of the versatile ionic-complementary peptide, FEFEFKFK, for such a purpose as this peptide spontaneously self-assembles into β-sheet-rich fibres that subsequently self-associate to form self-supporting hydrogels. Via simple live/dead cell assays, we demonstrated that 3 wt% hydrogels were optimal for the support of osteoblast cells. We went on to show that these cells are not only viable within the three-dimensional hydrogel but they also proliferate and produce osteogenic key proteins, that is, they behave like in vivo bone cells, over the 14-day period explored here. The gel elasticity increased over time when cells were present – in comparison to a decrease in control samples – indicating the deposition of matrix throughout the peptide scaffold. Moreover, significant quantities of calcium phosphate were deposited. Collectively, these data demonstrate that ionic-complementary octapeptides offer a suitable three-dimensional environment for osteoblastic cell function.
url https://doi.org/10.1177/2041731414539344
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AT albertosaiani humanosteoblastswithinsoftpeptidehydrogelspromotemineralisationinvitro
AT julieegough humanosteoblastswithinsoftpeptidehydrogelspromotemineralisationinvitro
AT alinefmiller humanosteoblastswithinsoftpeptidehydrogelspromotemineralisationinvitro
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