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Influence of Xenogeneic and Alloplastic Carriers for Bone Augmentation on Human Unrestricted Somatic Stem Cells
Authors:Lara Schorn,Anna Sine,Karin Berr,Jö  rg Handschel,Rita Depprich,Norbert R. Kü  bler,Christoph Sproll,Majeed Rana,Julian Lommen
Affiliation:1.Department of Oral-, Maxillofacial and Facial Plastic Surgery, University Hospital Düsseldorf, Moorenstr. 5, 40225 Düsseldorf, Germany; (A.S.); (K.B.); (R.D.); (N.R.K.); (C.S.); (M.R.); (J.L.);2.Medical School, Heinrich-Heine-University, Universitätsstr. 1, 40225 Düsseldorf, Germany;3.Klinik am Kaiserteich, Reichsstraße 59, 40217 Düsseldorf, Germany
Abstract:Alloplastic and xenogeneic bone grafting materials are frequently used for bone augmentation. The effect of these materials on precursor cells for bone augmentation is yet to be determined. The aim of this study was to ascertain, in vitro, how augmentation materials influence the growth rates and viability of human unrestricted somatic stem cells. The biocompatibility of two xenogeneic and one alloplastic bone graft was tested using human unrestricted somatic stem cells (USSCs). Proliferation, growth, survival and attachment of unrestricted somatic stem cells were monitored after 24 h, 48 h and 7 days. Furthermore, cell shape and morphology were evaluated by SEM. Scaffolds were assessed for their physical properties by Micro-CT imaging. USSCs showed distinct proliferation on the different carriers. Greatest proliferation was observed on the xenogeneic carriers along with improved viability of the cells. Pore sizes of the scaffolds varied significantly, with the xenogeneic materials providing greater pore sizes than the synthetic inorganic material. Unrestricted somatic stem cells in combination with a bovine collagenous bone block seem to be very compatible. A scaffold’s surface morphology, pore size and bioactive characteristics influence the proliferation, attachment and viability of USSCs.
Keywords:bone augmentation   dental bone substitute materials   xenogeneic bone grafts   alloplastic bone grafts   unrestricted somatic stem cells   bone regeneration
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