Biomaterial and implant induced ossification: in vitro and in vivo findings
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu kazuistiky, práce podpořená grantem, časopisecké články
PubMed
32415757
PubMed Central
PMC7496445
DOI
10.1002/term.3056
Knihovny.cz E-zdroje
- Klíčová slova
- bioactive glass, bioactivity, biomaterial-induced ossification, cranial implant, fiber-reinforced composite, osteogenesis,
- MeSH
- biokompatibilní materiály aplikace a dávkování MeSH
- lebka zranění metabolismus MeSH
- lidé středního věku MeSH
- lidé MeSH
- osteogeneze účinky léků MeSH
- protézy a implantáty * MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- kazuistiky MeSH
- práce podpořená grantem MeSH
- Názvy látek
- biokompatibilní materiály MeSH
Material-induced ossification is suggested as a suitable approach to heal large bone defects. Fiber-reinforced composite-bioactive glasses (FRC-BGs) display properties that could enhance the ossification of calvarial defects. Here, we analyzed the healing processes of a FRC-BG implant in vivo from the perspective of material-induced ossification. Histological analysis of the implant, which was removed 5 months after insertion, showed the formation of viable, noninflammatory mesenchymal tissue with newly-formed mineralized woven bone, as well as nonmineralized connective tissue with capillaries and larger blood vessels. The presence of osteocytes was detected within the newly generated bone matrix. To expand our understanding on the osteogenic properties of FRC-BG, we cultured human adipose tissue-derived mesenchymal stromal cells (AD-MSCs) in the presence of two different BGs (45S5 and S53P4) and Al2 O3 control. AD-MSCs grew and proliferated on all the scaffolds tested, as well as secreted abundant extracellular matrix, when osteogenic differentiation was appropriately stimulated. 45S5 and S53P4 induced enhanced expression of COL2A1, COL10A1, COL5A1 collagen subunits, and pro-osteogenic genes BMP2 and BMP4. The concomitant downregulation of BMP3 was also detected. Our findings show that FRC-BG can support the vascularization of the implant and the formation of abundant connective tissue in vivo. Specifically, BG 45S5 and BG S53P4 are suited to evoke the osteogenic potential of host mesenchymal stromal cells. In conclusion, FRC-BG implant demonstrated material-induced ossification both in vitro and in vivo.
Department of Oral Pathology and Radiology Institute of Dentistry University of Turku Turku Finland
Institute of Biomedicine University of Turku Turku Finland
International Clinical Research Center of St Anne's University Hospital Brno Brno Czech Republic
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