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Calcined Hydroxyapatite with Collagen I Foam Promotes Human MSC Osteogenic Differentiation
V. Hefka Blahnová, L. Vojtová, V. Pavliňáková, J. Muchová, E. Filová
Language English Country Switzerland
Document type Journal Article
Grant support
448218
Grant Agency of Charles University
CEITEC 2020 LQ1601
Ministry of Education, Youth and Sports of the Czech Republic
LO1508
Ministry of Education, Youth and Sports of the Czech Rep
LO1309
Ministry of Education, Youth and Sports of the Czech Republic
18-09306S
Czech Science Foundation
NLK
Free Medical Journals
from 2000
Freely Accessible Science Journals
from 2000
PubMed Central
from 2007
Europe PubMed Central
from 2007
ProQuest Central
from 2000-03-01
Open Access Digital Library
from 2000-01-01
Open Access Digital Library
from 2007-01-01
Health & Medicine (ProQuest)
from 2000-03-01
ROAD: Directory of Open Access Scholarly Resources
from 2000
PubMed
35457055
DOI
10.3390/ijms23084236
Knihovny.cz E-resources
- MeSH
- Cell Differentiation MeSH
- Durapatite * chemistry pharmacology MeSH
- Collagen Type I genetics MeSH
- Cells, Cultured MeSH
- Humans MeSH
- Osteogenesis * MeSH
- Tissue Engineering methods MeSH
- Tissue Scaffolds chemistry MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
Collagen I-based foams were modified with calcined or noncalcined hydroxyapatite or calcium phosphates with various particle sizes and pores to monitor their effect on cell interactions. The resulting scaffolds thus differed in grain size, changing from nanoscale to microscopic, and possessed diverse morphological characteristics and resorbability. The materials' biological action was shown on human bone marrow MSCs. Scaffold morphology was identified by SEM. Using viability test, qPCR, and immunohistochemical staining, we evaluated the biological activity of all of the materials. This study revealed that the most suitable scaffold composition for osteogenesis induction is collagen I foam with calcined hydroxyapatite with a pore size of 360 ± 130 μm and mean particle size of 0.130 μm. The expression of osteogenic markers RunX2 and ColI mRNA was promoted, and a strong synthesis of extracellular protein osteocalcin was observed. ColI/calcined HAP scaffold showed significant osteogenic potential, and can be easily manipulated and tailored to the defect size, which gives it great potential for bone tissue engineering applications.
References provided by Crossref.org
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