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Influence of collagen and chondroitin sulfate (CS) coatings on poly-(lactide-co-glycolide) (PLGA) on MG 63 osteoblast-like cells
M. Vandrovcová, T. Douglas, D. Hauk, B. Grössner-Schreiber, J. Wiltfang, L. Bačáková, P. H. Warnk
Jazyk angličtina Země Česko
Typ dokumentu práce podpořená grantem
NLK
Directory of Open Access Journals
od 1991
Free Medical Journals
od 1998
ProQuest Central
od 2005-01-01
Medline Complete (EBSCOhost)
od 2006-01-01
Nursing & Allied Health Database (ProQuest)
od 2005-01-01
Health & Medicine (ProQuest)
od 2005-01-01
ROAD: Directory of Open Access Scholarly Resources
od 1998
- MeSH
- biokompatibilní potahované materiály farmakologie chemie MeSH
- buněčné inženýrství metody MeSH
- buněčné linie MeSH
- chondroitinsulfáty farmakologie chemie MeSH
- kolagen typu I farmakologie chemie MeSH
- kultivované buňky MeSH
- kyselina mléčná chemie MeSH
- kyselina polyglykolová chemie MeSH
- lidé MeSH
- osteoblasty cytologie fyziologie účinky léků MeSH
- osteogeneze fyziologie účinky léků MeSH
- proliferace buněk účinky léků MeSH
- testování materiálů MeSH
- tkáňové podpůrné struktury MeSH
- viabilita buněk účinky léků MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- práce podpořená grantem MeSH
Poly-(lactide-co-glycolide) (PLGA) is an FDA-approved biodegradable polymer which has been widely used as a scaffold for tissue engineering applications. Collagen has been used as a coating material for bone contact materials, but relatively little interest has focused on biomimetic coating of PLGA with extracellular matrix components such as collagen and the glycosaminoglycan chondroitin sulfate (CS). In this study, PLGA films were coated with collagen type I or collagen I with CS (collagen I/CS) to investigate the effect of CS on the behaviour of the osteoblastic cell line MG 63. Collagen I/CS coatings promoted a significant increase in cell number after 3 days (in comparison to PLGA) and after 7 days (in comparison to PLGA and collagencoated PLGA). No influence of collagen I or collagen I/CS coatings on the spreading area after 1 day of culture was observed. However, the cells on collagen I/CS formed numerous filopodia and displayed well developed vinculin-containing focal adhesion plaques. Moreover, these cells contained a significantly higher concentration of osteocalcin, measured per mg of protein, than the cells on the pure collagen coating. Thus, it can be concluded that collagen I/CS coatings promote MG 63 cell proliferation, improve cell adhesion and enhance osteogenic cell differentiation.
Department of Biomaterials Radboud University Nijmegen Medical Center Nijmegen Netherlands
Department of Oral and Maxillofacial Surgery University of Kiel Kiel Germany
Faculty of Health Sciences and Medicine Bond University Gold Coast Queensland Australia
Institute of Physiology Academy of Sciences of the Czech Republic Prague
Citace poskytuje Crossref.org
Literatura
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