BMP-2 but not VEGF or PDGF in fibrin matrix supports bone healing in a delayed-union rat model

被引:67
作者
Kaipel, Martin [1 ,2 ]
Schuetzenberger, Sebastian [2 ]
Schultz, Arthur [2 ]
Ferguson, James [2 ]
Slezak, Paul [2 ]
Morton, Tatjana J. [2 ]
Van Griensven, Martijn [2 ]
Redl, Heinz [2 ]
机构
[1] Barmherzige Bruder Hosp, Dept Orthopaed, A-7000 Eisenstadt, Austria
[2] Ludwig Boltzmann Inst Expt & Clin Traumatol, A-1200 Vienna, Austria
关键词
PDGF; VEGF; BMP-2; fibrin; delayed-union; ENDOTHELIAL GROWTH-FACTOR; SIZE DEFECT MODEL; MORPHOGENETIC PROTEIN; DUAL DELIVERY; FACTOR-BB; REGENERATION; NONUNION; ANGIOGENESIS;
D O I
10.1002/jor.22132
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
100224 [整形外科学];
摘要
Treatment of delayed bone healing and non-unions after fractures, osteotomies or arthrodesis still is a relevant clinical challenge. Artificially applied growth factors can increase bone healing and progressively gain importance in clinical routine. The aim of this study was to determine the effects of rhPDGF-BB, rhVEGF-165, and rhBMP-2 in fibrin matrix on bone healing in a delayed-union rat model. Thirty-seven rats underwent a first operation where a standardized femoral critical size defect was created. A silicone spacer was implanted to impair vascularization within the defect. At 4 weeks the spacer was removed in a second operation and rhPDGF-BB, rhVEGF-165, or rhBMP-2 were applied in a fibrin clot. Animals in a fourth group received a fibrin clot without growth factors. At 8 weeks fibrin bound rhBMP-2 treated animals showed a significantly increased union rate and bone volume within the defect compared to the other groups. Single application of fibrin bound rhPDGF-BB and rhVEGF-165 failed to increase bone healing in our atrophic non-union model. (c) 2012 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 30:15631569, 2012
引用
收藏
页码:1563 / 1569
页数:7
相关论文
共 27 条
[1]
Recombinant Human Platelet-Derived Growth Factor BB (rhPDGF-BB) and Beta-Tricalcium Phosphate/Collagen Matrix Enhance Fracture Healing in a Diabetic Rat Model [J].
Al-Zube, Loay ;
Breitbart, Eric A. ;
O'Connor, J. Patrick ;
Parsons, J. Russell ;
Bradica, Gino ;
Hart, Charles E. ;
Lin, Sheldon S. .
JOURNAL OF ORTHOPAEDIC RESEARCH, 2009, 27 (08) :1074-1081
[2]
Beamer B, 2010, HSS J, V6, P85, DOI [10.1007/s11420-009-9129-4, DOI 10.1007/S11420-009-9129-4]
[3]
Benjamin LE, 1998, DEVELOPMENT, V125, P1591
[4]
Tissue engineering for bone defect heating: An update on a multi-component approach [J].
Drosse, Inga ;
Volkmer, Elias ;
Capanna, Rodolfo ;
De Biase, Pietro ;
Mutschler, Wolf ;
Schieker, Matthias .
INJURY-INTERNATIONAL JOURNAL OF THE CARE OF THE INJURED, 2008, 39 :S9-S20
[5]
Eckardt H, 2005, J BONE JOINT SURG BR, V87B, P1434, DOI 10.1302/0301-620X.87B10
[6]
Friedlaender GE, 2001, J BONE JOINT SURG AM, V83A, pS151
[7]
THE USE OF BONE MORPHOGENETIC PROTEIN IN THE TREATMENT OF NONUNION IN A CANINE MODEL [J].
HECKMAN, JD ;
BOYAN, BD ;
AUFDEMORTE, TB ;
ABBOTT, JT .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 1991, 73A (05) :750-764
[8]
Accelerated fracture healing in the geriatric, osteoporotic rat with recombinant human platelet-derived growth Factor-BB and an injectable beta-tricalcium phosphate/collagen matrix [J].
Hollinger, Jeffrey O. ;
Onikepe, Andrew O. ;
MacKrell, Jim ;
Einhorn, Thomas ;
Bradica, Gino ;
Lynch, Samuel ;
Hart, Charles E. .
JOURNAL OF ORTHOPAEDIC RESEARCH, 2008, 26 (01) :83-90
[9]
Human bone morphogenetic protein allografting for reconstruction of femoral nonunion [J].
Johnson, EE ;
Urist, MR .
CLINICAL ORTHOPAEDICS AND RELATED RESEARCH, 2000, (371) :61-74
[10]
Biological enhancement of tibial diaphyseal aseptic non-unions: the efficacy of autologous bone grafting, BMPs and reaming by-products [J].
Kanakaris, Nikolaos K. ;
Paliobeis, Christos ;
Manidakis, Nikolaos ;
Giannoudis, Peter V. .
INJURY-INTERNATIONAL JOURNAL OF THE CARE OF THE INJURED, 2007, 38 :S65-S75