Simvastatin coating of TiO2 scaffold induces osteogenic differentiation of human adipose tissue-derived mesenchymal stem cells

•Tissue engineering approach combining MSCs, simvastatin and a 3D porous scaffold.•Induction of osteogenic differentiation in MSCs by simvastatin coated scaffolds.•Lower concentration of simvastatin needed in 3D culture than reported for 2D culture.•A strategy for human adipose tissue-derived MSC ba...

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Veröffentlicht in:Biochemical and biophysical research communications 2014-04, Vol.447 (1), p.139-144
Hauptverfasser: Pullisaar, Helen, Reseland, Janne E., Haugen, Håvard J., Brinchmann, Jan E., Østrup, Esben
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container_issue 1
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container_title Biochemical and biophysical research communications
container_volume 447
creator Pullisaar, Helen
Reseland, Janne E.
Haugen, Håvard J.
Brinchmann, Jan E.
Østrup, Esben
description •Tissue engineering approach combining MSCs, simvastatin and a 3D porous scaffold.•Induction of osteogenic differentiation in MSCs by simvastatin coated scaffolds.•Lower concentration of simvastatin needed in 3D culture than reported for 2D culture.•A strategy for human adipose tissue-derived MSC based bone tissue engineering. Bone tissue engineering requires an osteoconductive scaffold, multipotent cells with regenerative capacity and bioactive molecules. In this study we investigated the osteogenic differentiation of human adipose tissue-derived mesenchymal stem cells (hAD-MSCs) on titanium dioxide (TiO2) scaffold coated with alginate hydrogel containing various concentrations of simvastatin (SIM). The mRNA expression of osteoblast-related genes such as collagen type I alpha 1 (COL1A1), alkaline phosphatase (ALPL), osteopontin (SPP1), osteocalcin (BGLAP) and vascular endothelial growth factor A (VEGFA) was enhanced in hAD-MSCs cultured on scaffolds with SIM in comparison to scaffolds without SIM. Furthermore, the secretion of osteoprotegerin (OPG), vascular endothelial growth factor A (VEGFA), osteopontin (OPN) and osteocalcin (OC) to the cell culture medium was higher from hAD-MSCs cultured on scaffolds with SIM compared to scaffolds without SIM. The TiO2 scaffold coated with alginate hydrogel containing SIM promote osteogenic differentiation of hAD-MSCs in vitro, and demonstrate feasibility as scaffold for hAD-MSC based bone tissue engineering.
doi_str_mv 10.1016/j.bbrc.2014.03.133
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Bone tissue engineering requires an osteoconductive scaffold, multipotent cells with regenerative capacity and bioactive molecules. In this study we investigated the osteogenic differentiation of human adipose tissue-derived mesenchymal stem cells (hAD-MSCs) on titanium dioxide (TiO2) scaffold coated with alginate hydrogel containing various concentrations of simvastatin (SIM). The mRNA expression of osteoblast-related genes such as collagen type I alpha 1 (COL1A1), alkaline phosphatase (ALPL), osteopontin (SPP1), osteocalcin (BGLAP) and vascular endothelial growth factor A (VEGFA) was enhanced in hAD-MSCs cultured on scaffolds with SIM in comparison to scaffolds without SIM. Furthermore, the secretion of osteoprotegerin (OPG), vascular endothelial growth factor A (VEGFA), osteopontin (OPN) and osteocalcin (OC) to the cell culture medium was higher from hAD-MSCs cultured on scaffolds with SIM compared to scaffolds without SIM. 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Bone tissue engineering requires an osteoconductive scaffold, multipotent cells with regenerative capacity and bioactive molecules. In this study we investigated the osteogenic differentiation of human adipose tissue-derived mesenchymal stem cells (hAD-MSCs) on titanium dioxide (TiO2) scaffold coated with alginate hydrogel containing various concentrations of simvastatin (SIM). The mRNA expression of osteoblast-related genes such as collagen type I alpha 1 (COL1A1), alkaline phosphatase (ALPL), osteopontin (SPP1), osteocalcin (BGLAP) and vascular endothelial growth factor A (VEGFA) was enhanced in hAD-MSCs cultured on scaffolds with SIM in comparison to scaffolds without SIM. Furthermore, the secretion of osteoprotegerin (OPG), vascular endothelial growth factor A (VEGFA), osteopontin (OPN) and osteocalcin (OC) to the cell culture medium was higher from hAD-MSCs cultured on scaffolds with SIM compared to scaffolds without SIM. 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Bone tissue engineering requires an osteoconductive scaffold, multipotent cells with regenerative capacity and bioactive molecules. In this study we investigated the osteogenic differentiation of human adipose tissue-derived mesenchymal stem cells (hAD-MSCs) on titanium dioxide (TiO2) scaffold coated with alginate hydrogel containing various concentrations of simvastatin (SIM). The mRNA expression of osteoblast-related genes such as collagen type I alpha 1 (COL1A1), alkaline phosphatase (ALPL), osteopontin (SPP1), osteocalcin (BGLAP) and vascular endothelial growth factor A (VEGFA) was enhanced in hAD-MSCs cultured on scaffolds with SIM in comparison to scaffolds without SIM. Furthermore, the secretion of osteoprotegerin (OPG), vascular endothelial growth factor A (VEGFA), osteopontin (OPN) and osteocalcin (OC) to the cell culture medium was higher from hAD-MSCs cultured on scaffolds with SIM compared to scaffolds without SIM. 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subjects Adipose Tissue - cytology
Adult
Alginate hydrogel
Cell Differentiation - drug effects
Cell Survival
Female
Human adipose tissue-derived mesenchymal stem cells
Humans
Mesenchymal Stromal Cells - drug effects
Mesenchymal Stromal Cells - physiology
Middle Aged
Osteocalcin - secretion
Osteogenesis
Osteopontin - secretion
Osteoprotegerin - secretion
RNA, Messenger - metabolism
Simvastatin
Simvastatin - pharmacology
TiO2 scaffold
Tissue Engineering - methods
Tissue Scaffolds
Titanium
Vascular Endothelial Growth Factor A - secretion
title Simvastatin coating of TiO2 scaffold induces osteogenic differentiation of human adipose tissue-derived mesenchymal stem cells
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