Bone Morphogenetic Protein-9 Is a Potent Chondrogenic and Morphogenic Factor for Articular Cartilage Chondroprogenitors.


Journal

Stem cells and development
ISSN: 1557-8534
Titre abrégé: Stem Cells Dev
Pays: United States
ID NLM: 101197107

Informations de publication

Date de publication:
07 2020
Historique:
pubmed: 5 5 2020
medline: 4 9 2021
entrez: 5 5 2020
Statut: ppublish

Résumé

Articular cartilage contains a subpopulation of tissue-specific progenitors that are an ideal cell type for cell therapies and generating neocartilage for tissue engineering applications. However, it is unclear whether the standard chondrogenic medium using transforming growth factor beta (TGFβ) isoforms is optimal to differentiate these cells. We therefore used pellet culture to screen progenitors from immature bovine articular cartilage with a number of chondrogenic factors and discovered that bone morphogenetic protein-9 (BMP9) precociously induces their differentiation. This difference was apparent with toluidine blue staining and confirmed by biochemical and transcriptional analyses with BMP9-treated progenitors exhibiting 11-fold and 5-fold greater aggrecan and collagen type II (COL2A1) gene expression than TGFβ1-treated progenitors. Quantitative gene expression analysis over 14 days highlighted the rapid and phased nature of BMP9-induced chondrogenesis with sequential activation of aggrecan then collagen type II, and negligible collagen type X gene expression. The extracellular matrix of TGFβ1-treated progenitors analyzed using atomic force microscopy was fibrillar and stiff whist BMP9-induced matrix of cells more compliant and correspondingly less fibrillar. Polarized light microscopy revealed an annular pattern of collagen fibril deposition typified by TGFβ1-treated pellets, whereas BMP9-treated pellets displayed a birefringence pattern that was more anisotropic. Remarkably, differentiated immature chondrocytes incubated as high-density cultures in vitro with BMP9 generated a pronounced anisotropic organization of collagen fibrils indistinguishable from mature adult articular cartilage, with cells in deeper zones arranged in columnar manner. This contrasted with cells grown with TGFβ1, where a concentric pattern of collagen fibrils was visualized within tissue pellets. In summary, BMP9 is a potent chondrogenic factor for articular cartilage progenitors and is also capable of inducing morphogenesis of adult-like cartilage, a highly desirable attribute for in vitro tissue-engineered cartilage.

Identifiants

pubmed: 32364057
doi: 10.1089/scd.2019.0209
pmc: PMC7374587
doi:

Substances chimiques

Growth Differentiation Factor 2 0
Collagen 9007-34-5
Hydroxyproline RMB44WO89X

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

882-894

Subventions

Organisme : Medical Research Council
ID : MR/L02280X/1
Pays : United Kingdom

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Auteurs

Ben J Morgan (BJ)

Centre of Nanohealth, Swansea University Medical School, Swansea, United Kingdom.

Guillermo Bauza-Mayol (G)

Centre of Nanohealth, Swansea University Medical School, Swansea, United Kingdom.

Oliver F W Gardner (OFW)

Centre of Nanohealth, Swansea University Medical School, Swansea, United Kingdom.
Stem Cells and Regenerative Medicine, UCL Great Ormond Street Institute of Child Health, London, United Kingdom.

Yadan Zhang (Y)

Centre of Nanohealth, Swansea University Medical School, Swansea, United Kingdom.

Riccardo Levato (R)

Department of Orthopaedics, University Medical Center Utrecht, Utrecht, the Netherlands.

Charles W Archer (CW)

Centre of Nanohealth, Swansea University Medical School, Swansea, United Kingdom.

Rene van Weeren (R)

Department of Equine Sciences, Faculty of Veterinary Medicine, Utrecht University, Utrecht, the Netherlands.

Jos Malda (J)

Department of Orthopaedics, University Medical Center Utrecht, Utrecht, the Netherlands.
Department of Equine Sciences, Faculty of Veterinary Medicine, Utrecht University, Utrecht, the Netherlands.

Robert Steven Conlan (RS)

Centre of Nanohealth, Swansea University Medical School, Swansea, United Kingdom.

Lewis W Francis (LW)

Centre of Nanohealth, Swansea University Medical School, Swansea, United Kingdom.

Ilyas M Khan (IM)

Centre of Nanohealth, Swansea University Medical School, Swansea, United Kingdom.

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Classifications MeSH