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Evaluation of the potential of chitosan/beta-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
- 1.0474278 - FGÚ 2018 RIV GB eng J - Journal Article
Przekora, A. - Vandrovcová, Marta - Trávníčková, Martina - Pajorová, Julia - Molitor, M. - Ginalska, G. - Bačáková, Lucie
Evaluation of the potential of chitosan/beta-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.
Biomedical Materials. Roč. 12, č. 1 (2017), č. článku 015030. ISSN 1748-6041. E-ISSN 1748-605X
R&D Projects: GA MZd(CZ) NV15-33018A
Institutional support: RVO:67985823
Keywords : runx2 * adipose-derived stem cells * bone marrow-derived stem cells * osteogenic differentiation
OECD category: Bioproducts (products that are manufactured using biological material as feedstock) biomaterials, bioplastics, biofuels, bioderived bulk and fine chemicals, bio-derived novel materials
Impact factor: 2.897, year: 2017
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/beta-1,3glucan/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 (-200mm Hg), as high negative pressure (-700mm Hg) applied during liposuction surgery may retard subsequent ADSC proliferation and type I collagen production.
Permanent Link: http://hdl.handle.net/11104/0271397
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