Integrated Multi-Assay Culture Model for Stem Cell Chondrogenic Differentiation

Recent osteochondral repair strategies highlight the promise of mesenchymal progenitors, an accessible stem cell source with osteogenic and chondrogenic potential, used in conjunction with biomaterials for tissue engineering. For this, regenerative medicine approaches require robust models to ensure...

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Main Authors: Amy Prosser, Colin Scotchford, George Roberts, David Grant, Virginie Sottile
Format: Article
Language:English
Published: MDPI AG 2019-02-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/20/4/951
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spelling doaj-825f523eb778486a9dc0583272c1d6942020-11-25T00:59:50ZengMDPI AGInternational Journal of Molecular Sciences1422-00672019-02-0120495110.3390/ijms20040951ijms20040951Integrated Multi-Assay Culture Model for Stem Cell Chondrogenic DifferentiationAmy Prosser0Colin Scotchford1George Roberts2David Grant3Virginie Sottile4Wolfson STEM Centre, School of Medicine, University of Nottingham, Nottingham NG7 2RD, UKAdvanced Biomaterials Research Group, Faculty of Engineering, University of Nottingham, Nottingham NG7 2RD, UKAdvanced Biomaterials Research Group, Faculty of Engineering, University of Nottingham, Nottingham NG7 2RD, UKAdvanced Biomaterials Research Group, Faculty of Engineering, University of Nottingham, Nottingham NG7 2RD, UKWolfson STEM Centre, School of Medicine, University of Nottingham, Nottingham NG7 2RD, UKRecent osteochondral repair strategies highlight the promise of mesenchymal progenitors, an accessible stem cell source with osteogenic and chondrogenic potential, used in conjunction with biomaterials for tissue engineering. For this, regenerative medicine approaches require robust models to ensure selected cell populations can generate the desired cell type in a reproducible and measurable manner. Techniques for in vitro chondrogenic differentiation are well-established but largely qualitative, relying on sample staining and imaging. To facilitate the in vitro screening of pro-chondrogenic treatments, a 3D micropellet culture combined with three quantitative GAG assays has been developed, with a fourth parallel assay measuring sample content to enable normalisation. The effect of transforming growth factor beta (TGF-β) used to validate this culture format produced a measurable increase in proteoglycan production in the parallel assays, in both 2D and 3D culture configurations. When compared to traditional micropellets, the monolayer format appeared less able to detect changes in cell differentiation, however in-well 3D cultures displayed a significant differential response. Effects on collagen 2 expression confirmed these observations. Based on these results, a microplate format was optimised for 3D culture, in a high-throughput in-well configuration. This model showed improved sensitivity and confirmed the 3D micropellet in-well quantitative assays as an effective differentiation format compatible with streamlined, high-throughput chondrogenic screens.https://www.mdpi.com/1422-0067/20/4/951stem cell differentiation3D culturechondrogenesismultimodal analysisquantitative assay
collection DOAJ
language English
format Article
sources DOAJ
author Amy Prosser
Colin Scotchford
George Roberts
David Grant
Virginie Sottile
spellingShingle Amy Prosser
Colin Scotchford
George Roberts
David Grant
Virginie Sottile
Integrated Multi-Assay Culture Model for Stem Cell Chondrogenic Differentiation
International Journal of Molecular Sciences
stem cell differentiation
3D culture
chondrogenesis
multimodal analysis
quantitative assay
author_facet Amy Prosser
Colin Scotchford
George Roberts
David Grant
Virginie Sottile
author_sort Amy Prosser
title Integrated Multi-Assay Culture Model for Stem Cell Chondrogenic Differentiation
title_short Integrated Multi-Assay Culture Model for Stem Cell Chondrogenic Differentiation
title_full Integrated Multi-Assay Culture Model for Stem Cell Chondrogenic Differentiation
title_fullStr Integrated Multi-Assay Culture Model for Stem Cell Chondrogenic Differentiation
title_full_unstemmed Integrated Multi-Assay Culture Model for Stem Cell Chondrogenic Differentiation
title_sort integrated multi-assay culture model for stem cell chondrogenic differentiation
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1422-0067
publishDate 2019-02-01
description Recent osteochondral repair strategies highlight the promise of mesenchymal progenitors, an accessible stem cell source with osteogenic and chondrogenic potential, used in conjunction with biomaterials for tissue engineering. For this, regenerative medicine approaches require robust models to ensure selected cell populations can generate the desired cell type in a reproducible and measurable manner. Techniques for in vitro chondrogenic differentiation are well-established but largely qualitative, relying on sample staining and imaging. To facilitate the in vitro screening of pro-chondrogenic treatments, a 3D micropellet culture combined with three quantitative GAG assays has been developed, with a fourth parallel assay measuring sample content to enable normalisation. The effect of transforming growth factor beta (TGF-β) used to validate this culture format produced a measurable increase in proteoglycan production in the parallel assays, in both 2D and 3D culture configurations. When compared to traditional micropellets, the monolayer format appeared less able to detect changes in cell differentiation, however in-well 3D cultures displayed a significant differential response. Effects on collagen 2 expression confirmed these observations. Based on these results, a microplate format was optimised for 3D culture, in a high-throughput in-well configuration. This model showed improved sensitivity and confirmed the 3D micropellet in-well quantitative assays as an effective differentiation format compatible with streamlined, high-throughput chondrogenic screens.
topic stem cell differentiation
3D culture
chondrogenesis
multimodal analysis
quantitative assay
url https://www.mdpi.com/1422-0067/20/4/951
work_keys_str_mv AT amyprosser integratedmultiassayculturemodelforstemcellchondrogenicdifferentiation
AT colinscotchford integratedmultiassayculturemodelforstemcellchondrogenicdifferentiation
AT georgeroberts integratedmultiassayculturemodelforstemcellchondrogenicdifferentiation
AT davidgrant integratedmultiassayculturemodelforstemcellchondrogenicdifferentiation
AT virginiesottile integratedmultiassayculturemodelforstemcellchondrogenicdifferentiation
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