Cited by 101Bone Tissue Engineering MaterialsTissue Engineering and Regenerative MedicineCollagen: Extraction and Characterization

Development of specific collagen scaffolds to support the osteogenic and chondrogenic differentiation of human bone marrow stromal cells

Dawson, Jonathan I., Wahl, Denys A., Lanham, Stuart A., Kanczler, Janos M., Czernuszka, Jan T., Oreffo, Richard O.C.·2008·Biomaterials

Abstract

Type I Collagen matrices of defined porosity, incorporating carbonate substituted hydroxyapatite (HA) crystals, were assessed for their ability to support osteo- and chondrogenic differentiation of human bone marrow stromal cells (HBMSCs). Collagen-HA composite scaffolds supported the osteogenic differentiation of HBMSCs both in vitro and in vivo as demonstrated by histological and micro-CT analyses indicating the extensive penetration of alkaline phosphatase expressing cells and new matrix synthesis with localised areas immunologically positive for osteocalcin. In vivo, extensive new osteoid formation of implant origin was observed in the areas of vasculature. Chondrogenic matrix synthesis was evidenced in the peripheral regions of pure collagen systems by an abundance of Sox9 expressing chondrocytes embedded within a proteoglycan and collagen II rich ECM. The introduction of microchannels to the scaffold architecture was seen to enhance chondrogenesis. Tissue specific gene expression and corresponding matrix synthesis indicate that collagen matrices support the growth and differentiation of HBMSCs and suggest the potential of this platform for understanding the ECM cues necessary for osteogenesis and chondrogenesis.

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Crossref · 10.1016/j.biomaterials.2008.03.040

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  • Composite scaffolds based on collagen and HA enhanced the biological properties of seeded cells, resulting in a higher proliferation and differentiation rate, leading to bone regeneration.

    “Another study determined that composite scaffolds based on collagen and HA enhanced the biological properties of seeded cells, which resulted in a higher proliferation and differentiation rate, leading to bone regeneration [63].”

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Authors
Dawson, J. I., Wahl, D. A., Lanham, S. A., Kanczler, J. M., Czernuszka, J. T., & Oreffo, R. O. C.
Affiliations
  • Southampton General Hospital (GB)
  • University of Oxford (GB)
Corresponding author
Dawson, Jonathan I.
Venue
Biomaterials
Publisher
Elsevier BV
Published
2008-07
Volume
29
Issue
21
Pages
3105-3116
ISSN
0142-9612 (ISSN-L)
OpenAlex
W2022790300
Cited by
101
References
1
Citations by year
2026: 1 · 2025: 1 · 2024: 1 · 2023: 3 · 2022: 2 · 2021: 6 · 2020: 6 · 2019: 5 · 2018: 3 · 2017: 5 · 2016: 5 · 2015: 5 · 2014: 8 · 2013: 6 · 2012: 11
FWCI
6.91
Type
journal article
Language
en
Open access
closed
Locations
  • Biomaterials (publishedVersion)
  • PubMed (publishedVersion)
  • ePrints Soton (University of Southampton) (submittedVersion)
Funders
Biotechnology and Biological Sciences Research Council
Topics
  • Physical Sciences › Engineering › Biomedical Engineering › Bone Tissue Engineering Materials
  • Health Sciences › Medicine › Surgery › Tissue Engineering and Regenerative Medicine
  • Physical Sciences › Materials Science › Biomaterials › Collagen: Extraction and Characterization
Keywords
collagen scaffolds, type I collagen, hydroxyapatite, mesenchymal stem cells, osteogenic differentiation, chondrogenic differentiation, osteoinduction, microchannels, extracellular matrix, SOX9, osteocalcin, alkaline phosphatase, osteoid formation, tissue engineering
MeSH terms
Biocompatible Materials, Bone Marrow Cells, Cell Differentiation, Cell Survival, Collagen, Humans, Microscopy, Electron, Scanning, Osteogenesis, Stromal Cells, Chondrogenesis, Tissue Engineering, Tissue Scaffolds

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