Quantifying migration and polarization of murine mesenchymal stem cells on different bone substitutes by confocal laser scanning microscopy

• Published in: Journal of cranio-maxillo-facial surgery 2010-12, Vol.38 (8), p.580-588
• Main Authors: Roldán, J.C, Chang, E, Kelantan, M, Jazayeri, L, Deisinger, U, Detsch, R, Reichert, T.E, Gurtner, G.C
• Format: Article
• Language: English
• Subjects: Animals; Biological and medical sciences; Bone Regeneration - physiology; bone substitutes; Bone Substitutes - chemistry; Calcium Phosphates - chemistry; Cattle; cell migration; Cell Movement - physiology; cell polarity; Cell Polarity - physiology; Cells, Cultured; Ceramics - chemistry; confocal scanning laser microscopy; Dentistry; green fluorescent protein; Medical sciences; mesenchymal stem cells; Mesenchymal Stromal Cells - cytology; Mice; Minerals - chemistry; Neovascularization, Physiologic - physiology; Osseointegration - physiology; Otorhinolaryngology. Stomatology; Surgery; Tissue Engineering; Tissue Scaffolds - chemistry
• ISSN: 1010-5182; 1878-4119
• DOI: 10.1016/j.jcms.2010.01.004

Summary Introduction Cell migration is preceded by cell polarization. The aim of the present study was to evaluate the impact of the geometry of different bone substitutes on cell morphology and chemical responses in vitro. Materials and methods Cell polarization and migration were monitored temporally by using confocal laser scanning microscopy (CLSM) to follow green fluorescent protein (GFP) ± mesenchymal stem cells (MSCs) on anorganic cancellous bovine bone (Bio-Oss® ), β-tricalcium phosphate (β-TCP) (chronOS® ) and highly porous calcium phosphate ceramics (Friedrich-Baur-Research-Institute for Biomaterials, Germany). Differentiation GFP ± MSCs was observed using pro-angiogenic and pro-osteogenic biomarkers. Results At the third day of culture polarized vs. non-polarized cellular sub-populations were clearly established. Biomaterials that showed more than 40% of polarized cells at the 3rd day of culture, subsequently showed an enhanced cell migration compared to biomaterials, where non-polarized cells predominated ( p < 0.003). This trend continued untill the 7th day of culture ( p < 0.003). The expression of vascular endothelial growth factor was enhanced in biomaterials where cell polarization predominated at the 7th day of culture ( p = 0.001). Conclusions This model opens an interesting approach to understand osteoconductivity at a cellular level. MSCs are promising in bone tissue engineering considering the strong angiogenic effect before differentiation occurs.