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Volume 38, Issue 6, Pages 423-430 (September 2010)


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Bone formation and degradation of a highly porous biphasic calcium phosphate ceramic in presence of BMP-7, VEGF and mesenchymal stem cells in an ectopic mouse model

J.C. Roldán1Corresponding Author Informationemail address, R. Detsch2, S. Schaefer3, E. Chang4, M. Kelantan4, W. Waiss1, T.E. Reichert1, G.C. Gurtner4, U. Deisinger3Corresponding Author Informationemail address

Received 19 September 2009; accepted 19 January 2010. published online 02 March 2010.

Summary 

Introduction

Angiogenesis and mesenchymal stem cells (MSCs) promote osteogenesis. The aim of the present study was to evaluate whether bone morphogenetic protein (BMP-7) promoted osteoinduction could be enhanced by combining it with vascular endothelial growth factor (VEGF) or MSCs in highly porous biphasic calcium phosphate (BCP) ceramics.

Materials and methods

BCP ceramic blocks were implanted in an ectopic site in 24 mice (BMP-7 vs. BMP-7/VEGF; BMP-7 vs. BMP-7/MSCs and BMP-7 vs. Control; each group n=8). Specimens were analysed 12 weeks after surgery by environmental scanning electron microscopy (ESEM) and Giemsa staining.

Results

In all implanted scaffolds, newly formed bone was observed, even in the control site. No statistical differences in the amount of new bone were found in the presence of BMP-7 compared to BMP-7/VEGF (p=1.0) or BMP-7/MSCs (p=0.786). ESEM revealed a degradation of the scaffolds. A higher degradation was observed in areas where no bone-implant contact was present compared to areas where the ceramic was integrated in newly formed bone.

Conclusions

Neither VEGF nor MSCs enhanced BMP-7 induced bone formation under the selected conditions. The present ceramic seemed to be osteoinductive and degradable, making this material suitable for bone tissue engineering.

1 Department of Cranio-Maxillofacial Surgery, University of Regensburg, Germany

2 BioCer Entwicklungs-GmbH, Bayreuth, Germany

3 Friedrich-Baur-Research-Institute for Biomaterials, University of Bayreuth, Germany

4 Laboratory for Microvascular Surgery and Vascular Tissue Engineering, Stanford University, CA, USA

Corresponding Author InformationJ. Camilo ROLDÁN, MD, DMD, Department of Oral & Maxillofacial Plastic Surgery, University of Regensburg, Germany.

Corresponding Author InformationUlrike DEISINGER, PhD, Friedrich-Baur-Research-Institute for Biomaterials, University of Bayreuth, Germany

PII: S1010-5182(10)00015-6

doi:10.1016/j.jcms.2010.01.003


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