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Evaluation of the potential of chitosan/β-1,3-glucan/hydroxyapatite material as a scaffold for living bone graft production in vitro by comparison of ADSC and BMDSC behaviour on its surface
Agata Przekora, Marta Vandrovcova, Martina Travnickova, Julia Pajorova, Martin Molitor, Grazyna Ginalska, Lucie Bacakova
Jazyk angličtina Země Velká Británie
Grantová podpora
NV15-33018A
MZ0
CEP - Centrální evidence projektů
PubMed
28054934
DOI
10.1088/1748-605x/aa56f9
Knihovny.cz E-zdroje
- MeSH
- beta-glukany chemie MeSH
- biokompatibilní materiály chemie MeSH
- buněčná diferenciace MeSH
- chitosan chemie MeSH
- fokální adheze MeSH
- hydroxyapatit chemie MeSH
- kultivované buňky MeSH
- lidé MeSH
- mezenchymální kmenové buňky cytologie fyziologie MeSH
- osteogeneze MeSH
- pohyb buněk MeSH
- proliferace buněk MeSH
- regenerace kostí MeSH
- testování materiálů MeSH
- tkáňové podpůrné struktury chemie MeSH
- tuková tkáň cytologie MeSH
- Check Tag
- lidé MeSH
The opinion regarding the origin of adult stem cells that should be used for living bone construct generation is strongly divided in the scientific community. In this study, the potential of chitosan/β-1,3-glucan/hydroxyapatite (chit/glu/HA) material as a scaffold for bone regeneration applications was evaluated by behaviour comparison of adult stem cells derived from both origins-adipose derived mesenchymal stem cell (ADSC) tissue and bone marrow derived mesenchymal stem cells (BMDSCs). In the case of ADSC isolation, low and high negative pressures were applied during a liposuction procedure in order to determine if negative pressure settings may have an impact on subsequent cell behaviour in vitro. The obtained results demonstrated that the chit/glu/HA material is a promising candidate to be used for living bone graft production in vitro as both ADSCs and BMDSCs revealed a satisfactory proliferation and differentiation ability on its surface. Nevertheless, BMDSCs would be a better choice of adult stem cells since they were better spread, more strongly attached and showed a more superior proliferation and differentiation ability than ADSCs when cultured on the chit/glu/HA scaffold. However, if BMDSCs cannot be isolated, ADSCs may be used for bone construct production but lipoaspirate should be collected under low negative pressure (-200 mm Hg), as high negative pressure (-700 mmHg) applied during liposuction surgery may retard subsequent ADSC proliferation and type I collagen production.
Citace poskytuje Crossref.org
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