The University of Southampton
University of Southampton Institutional Repository

An ex vivo model for chondrogenesis and osteogenesis

An ex vivo model for chondrogenesis and osteogenesis
An ex vivo model for chondrogenesis and osteogenesis
Loss of bone and cartilage are major healthcare issues. At present, there is a paucity of therapies for effectively repairing these tissues sustainably in the long term. A tissue engineering approach using advanced functional scaffolds may provide a clinically acceptable alternative. In this study, an innovative mineralized alginate/chitosan scaffold was used to provide tailored microenvironments for driving chondrogenesis and osteogenesis from single and mixed populations of human articular chondrocytes and human bone marrow stromal cells. Polysaccharide capsules were prepared with combinations of these cell types with the addition of type I or type II collagen to augment cell-matrix interactions and promote the formation of phenotypically distinct tissues and placed in a rotating (Synthecon) bioreactor or held in static 2D culture conditions for up to 28 days. Significant cell-generated matrix synthesis was observed in human bone marrow bioreactor samples containing type I collagen after 21-28 days, with increased cell proliferation, cell activity and osteocalcin synthesis. The cell-generated matrix was immuno-positive for types I and II collagen, bone sialoprotein and type X collagen, a marker of chondrogenic hypertrophy, demonstrating the formation of a mature chondrogenic phenotype with areas of new osteoid tissue formation. We present a unique approach using alginate/collagen capsules encapsulated in chitosan to promote chondrogenic and osteogenic differentiation and extracellular matrix formation and the potential for tissue-specific differentiation. This has significant implications for skeletal regeneration and application.
cartilage, osteogenesis, alginate, polysaccharide, bioreactor, origins, hexuronic acids, male, aged, phenotype, cell proliferation, collagen type ii, chondrocytes, therapy, humans, bone marrow cells, chemistry, osteocalcin, alginates, drug effects, pharmacology, activity, tissue engineering, collagen type i, bone, extracellular matrix, glucuronic acid, biocompatible materials, time factors, aged 80 and over, chondrogenesis, cytology, methods, capsules, regeneration, stromal cells, research, acid, health, bone marrow, middle aged, female, chitosan, immunohistochemistry, human, disease
0142-9612
2839-2849
Pound, Jodie C.
74b8055f-3f23-4fb4-8c20-4823302dc10a
Green, David W.
9591e846-aeac-4549-b389-1744c5a43cff
Roach, Helmtrud I.
ca2ff1f4-1ada-4c56-9097-cd27ca4d199e
Mann, Stephen
1cbb2d4f-aee2-403c-9950-18bd388f02c0
Oreffo, Richard O.C.
ff9fff72-6855-4d0f-bfb2-311d0e8f3778
Pound, Jodie C.
74b8055f-3f23-4fb4-8c20-4823302dc10a
Green, David W.
9591e846-aeac-4549-b389-1744c5a43cff
Roach, Helmtrud I.
ca2ff1f4-1ada-4c56-9097-cd27ca4d199e
Mann, Stephen
1cbb2d4f-aee2-403c-9950-18bd388f02c0
Oreffo, Richard O.C.
ff9fff72-6855-4d0f-bfb2-311d0e8f3778

Pound, Jodie C., Green, David W., Roach, Helmtrud I., Mann, Stephen and Oreffo, Richard O.C. (2007) An ex vivo model for chondrogenesis and osteogenesis. Biomaterials, 28 (18), 2839-2849. (doi:10.1016/j.biomaterials.2007.02.029).

Record type: Article

Abstract

Loss of bone and cartilage are major healthcare issues. At present, there is a paucity of therapies for effectively repairing these tissues sustainably in the long term. A tissue engineering approach using advanced functional scaffolds may provide a clinically acceptable alternative. In this study, an innovative mineralized alginate/chitosan scaffold was used to provide tailored microenvironments for driving chondrogenesis and osteogenesis from single and mixed populations of human articular chondrocytes and human bone marrow stromal cells. Polysaccharide capsules were prepared with combinations of these cell types with the addition of type I or type II collagen to augment cell-matrix interactions and promote the formation of phenotypically distinct tissues and placed in a rotating (Synthecon) bioreactor or held in static 2D culture conditions for up to 28 days. Significant cell-generated matrix synthesis was observed in human bone marrow bioreactor samples containing type I collagen after 21-28 days, with increased cell proliferation, cell activity and osteocalcin synthesis. The cell-generated matrix was immuno-positive for types I and II collagen, bone sialoprotein and type X collagen, a marker of chondrogenic hypertrophy, demonstrating the formation of a mature chondrogenic phenotype with areas of new osteoid tissue formation. We present a unique approach using alginate/collagen capsules encapsulated in chitosan to promote chondrogenic and osteogenic differentiation and extracellular matrix formation and the potential for tissue-specific differentiation. This has significant implications for skeletal regeneration and application.

This record has no associated files available for download.

More information

Published date: June 2007
Keywords: cartilage, osteogenesis, alginate, polysaccharide, bioreactor, origins, hexuronic acids, male, aged, phenotype, cell proliferation, collagen type ii, chondrocytes, therapy, humans, bone marrow cells, chemistry, osteocalcin, alginates, drug effects, pharmacology, activity, tissue engineering, collagen type i, bone, extracellular matrix, glucuronic acid, biocompatible materials, time factors, aged 80 and over, chondrogenesis, cytology, methods, capsules, regeneration, stromal cells, research, acid, health, bone marrow, middle aged, female, chitosan, immunohistochemistry, human, disease

Identifiers

Local EPrints ID: 48493
URI: http://eprints.soton.ac.uk/id/eprint/48493
ISSN: 0142-9612
PURE UUID: fc029b23-b85f-4bd1-82aa-160a8a12f201
ORCID for Richard O.C. Oreffo: ORCID iD orcid.org/0000-0001-5995-6726

Catalogue record

Date deposited: 26 Sep 2007
Last modified: 16 Mar 2024 03:11

Export record

Altmetrics

Contributors

Author: Jodie C. Pound
Author: David W. Green
Author: Helmtrud I. Roach
Author: Stephen Mann

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×