Analysis of the Intrinsic Self-Organising Properties of Mesenchymal Stromal Cells in Three-Dimensional Co-Culture Models with Endothelial Cells

Mesenchymal stem/stromal cells (MSCs) are typically characterised by their ability to differentiate into skeletal (osteogenic, chondrogenic and adipogenic) lineages. MSCs also appear to have additional non-stem cell functions in coordinating tissue morphogenesis and organising vascular networks thro...

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Main Authors: Julia Marshall, Amanda Barnes, Paul Genever
Format: Article
Language:English
Published: MDPI AG 2018-10-01
Series:Bioengineering
Subjects:
Online Access:https://www.mdpi.com/2306-5354/5/4/92
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spelling doaj-e3d1da1c51d74a6aa58803c17eb8ce1c2020-11-24T21:45:45ZengMDPI AGBioengineering2306-53542018-10-01549210.3390/bioengineering5040092bioengineering5040092Analysis of the Intrinsic Self-Organising Properties of Mesenchymal Stromal Cells in Three-Dimensional Co-Culture Models with Endothelial CellsJulia Marshall0Amanda Barnes1Paul Genever2Department of Biology, University of York, York YO10 5DD, UKDepartment of Biology, University of York, York YO10 5DD, UKDepartment of Biology, University of York, York YO10 5DD, UKMesenchymal stem/stromal cells (MSCs) are typically characterised by their ability to differentiate into skeletal (osteogenic, chondrogenic and adipogenic) lineages. MSCs also appear to have additional non-stem cell functions in coordinating tissue morphogenesis and organising vascular networks through interactions with endothelial cells (ECs). However, suitable experimental models to examine these apparently unique MSC properties are lacking. Following previous work, we have developed our 3D in vitro co-culture models to enable us to track cellular self-organisation events in heterotypic cell spheroids combining ECs, MSCs and their differentiated progeny. In these systems, MSCs, but not related fibroblastic cell types, promote the assembly of ECs into interconnected networks through intrinsic mechanisms, dependent on the relative abundance of MSC and EC numbers. Perturbation of endogenous platelet-derived growth factor (PDGF) signalling significantly increased EC network length, width and branching. When MSCs were pre-differentiated towards an osteogenic or chondrogenic lineage and co-cultured as mixed 3D spheroids, they segregated into polarised osseous and chondral regions. In the presence of ECs, the pre-differentiated MSCs redistributed to form a central mixed cell core with an outer osseous layer. Our findings demonstrate the intrinsic self-organising properties of MSCs, which may broaden their use in regenerative medicine and advance current approaches.https://www.mdpi.com/2306-5354/5/4/923D in vitro modelsMSCsendothelial cellsosteoblastschondrocytesself-organisationvascularizationregenerative medicine
collection DOAJ
language English
format Article
sources DOAJ
author Julia Marshall
Amanda Barnes
Paul Genever
spellingShingle Julia Marshall
Amanda Barnes
Paul Genever
Analysis of the Intrinsic Self-Organising Properties of Mesenchymal Stromal Cells in Three-Dimensional Co-Culture Models with Endothelial Cells
Bioengineering
3D in vitro models
MSCs
endothelial cells
osteoblasts
chondrocytes
self-organisation
vascularization
regenerative medicine
author_facet Julia Marshall
Amanda Barnes
Paul Genever
author_sort Julia Marshall
title Analysis of the Intrinsic Self-Organising Properties of Mesenchymal Stromal Cells in Three-Dimensional Co-Culture Models with Endothelial Cells
title_short Analysis of the Intrinsic Self-Organising Properties of Mesenchymal Stromal Cells in Three-Dimensional Co-Culture Models with Endothelial Cells
title_full Analysis of the Intrinsic Self-Organising Properties of Mesenchymal Stromal Cells in Three-Dimensional Co-Culture Models with Endothelial Cells
title_fullStr Analysis of the Intrinsic Self-Organising Properties of Mesenchymal Stromal Cells in Three-Dimensional Co-Culture Models with Endothelial Cells
title_full_unstemmed Analysis of the Intrinsic Self-Organising Properties of Mesenchymal Stromal Cells in Three-Dimensional Co-Culture Models with Endothelial Cells
title_sort analysis of the intrinsic self-organising properties of mesenchymal stromal cells in three-dimensional co-culture models with endothelial cells
publisher MDPI AG
series Bioengineering
issn 2306-5354
publishDate 2018-10-01
description Mesenchymal stem/stromal cells (MSCs) are typically characterised by their ability to differentiate into skeletal (osteogenic, chondrogenic and adipogenic) lineages. MSCs also appear to have additional non-stem cell functions in coordinating tissue morphogenesis and organising vascular networks through interactions with endothelial cells (ECs). However, suitable experimental models to examine these apparently unique MSC properties are lacking. Following previous work, we have developed our 3D in vitro co-culture models to enable us to track cellular self-organisation events in heterotypic cell spheroids combining ECs, MSCs and their differentiated progeny. In these systems, MSCs, but not related fibroblastic cell types, promote the assembly of ECs into interconnected networks through intrinsic mechanisms, dependent on the relative abundance of MSC and EC numbers. Perturbation of endogenous platelet-derived growth factor (PDGF) signalling significantly increased EC network length, width and branching. When MSCs were pre-differentiated towards an osteogenic or chondrogenic lineage and co-cultured as mixed 3D spheroids, they segregated into polarised osseous and chondral regions. In the presence of ECs, the pre-differentiated MSCs redistributed to form a central mixed cell core with an outer osseous layer. Our findings demonstrate the intrinsic self-organising properties of MSCs, which may broaden their use in regenerative medicine and advance current approaches.
topic 3D in vitro models
MSCs
endothelial cells
osteoblasts
chondrocytes
self-organisation
vascularization
regenerative medicine
url https://www.mdpi.com/2306-5354/5/4/92
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AT paulgenever analysisoftheintrinsicselforganisingpropertiesofmesenchymalstromalcellsinthreedimensionalcoculturemodelswithendothelialcells
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