The use of a cartilage decellularized matrix scaffold for the repair of osteochondral defects: the importance of long-term studies in a large animal model

被引:40
作者
Bolanos, R. A. Vindas [1 ]
Cokelaere, S. M. [2 ]
McDermott, J. M. Estrada [1 ]
Benders, K. E. M. [3 ]
Gbureck, U. [4 ]
Plomp, S. G. M. [2 ]
Weinans, H. [3 ]
Groll, J. [4 ]
van Weeren, P. R. [2 ]
Malda, J. [2 ,3 ]
机构
[1] Univ Nacl, Escuela Med Vet, Catedra Cirugia Especies Mayores, Heredia, Costa Rica
[2] Univ Utrecht, Fac Vet Med, Dept Equine Sci, Utrecht, Netherlands
[3] Univ Med Ctr Utrecht, Dept Orthopaed, Div Surg, Utrecht, Netherlands
[4] Univ Wurzburg, Dept Funct Mat Med & Dent, D-97070 Wurzburg, Germany
基金
欧洲研究理事会;
关键词
Animal models; Cartilage; Scaffolds; Equine model; Long-term study; Osteochondral defect; ARTICULAR-CARTILAGE; EXTRACELLULAR-MATRIX; REGENERATION; CHONDROCYTES; IMPLANTS; TISSUE; EQUINE; CELLS; SITE;
D O I
10.1016/j.joca.2016.08.005
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
摘要
Objective: To investigate the effect of decellularized cartilage -derived matrix (CDM) scaffolds, by itself and as a composite scaffold with a calcium phosphate (CaP) base, for the repair of osteochondral defects. It was hypothesized that the chondral defects would heal with fibrocartilaginous tissue and that the composite scaffold would result in better bone formation. Methods: After an 8-week pilot experiment in a single horse, scaffolds were implanted in eight healthy horses in osteochondral defects on the medial trochlear ridge of the femur. In one joint a composite CDM CaP scaffold was implanted (+P), in the contralateral joint a CDM only (-P) scaffold. After euthanasia at 6 months, tissues were analysed by histology, immunohistochemistry, micro-CT, biochemistry and biomechanical evaluation. Results: The 8-week pilot showed encouraging formation of bone and cartilage, but incomplete defect filling. At 6 months, micro-CT and histology showed much more limited filling of the defect, but the CaP component of the +P scaffolds was well integrated with the surrounding bone. The repair tissue was fibrotic with high collagen type I and low type II content and with no differences between the groups. There were also no biochemical differences between the groups and repair tissue was much less stiff than normal tissue (P < 0.0001). Conclusions: The implants failed to produce reasonable repair tissue in this osteochondral defect model, although the CaP base in the P group integrated well with the recipient bone. The study stresses the importance of long-term in vivo studies to assess the efficacy of cartilage repair techniques. (C) 2016 Osteoarthritis Research Society International. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:413 / 420
页数:8
相关论文
共 31 条
[1]   Preclinical animal models in single site cartilage defect testing: a systematic review [J].
Ahern, B. J. ;
Parvizi, J. ;
Boston, R. ;
Schaer, T. P. .
OSTEOARTHRITIS AND CARTILAGE, 2009, 17 (06) :705-713
[2]   The extracellular matrix as a biologic scaffold material [J].
Badylak, Stephen F. .
BIOMATERIALS, 2007, 28 (25) :3587-3593
[3]   One-stage focal cartilage defect treatment with bone marrow mononuclear cells and chondrocytes leads to better macroscopic cartilage regeneration compared to microfracture in goats [J].
Bekkers, J. E. J. ;
Creemers, L. B. ;
Tsuchida, A. I. ;
van Rijen, M. H. P. ;
Custers, R. J. H. ;
Dhert, W. J. A. ;
Saris, D. B. E. .
OSTEOARTHRITIS AND CARTILAGE, 2013, 21 (07) :950-956
[4]   Multipotent Stromal Cells Outperform Chondrocytes on Cartilage-Derived Matrix Scaffolds [J].
Benders, K. E. M. ;
Boot, W. ;
Cokelaere, S. M. ;
Van Weeren, P. R. ;
Gawlitta, D. ;
Bergman, H. J. ;
Saris, D. B. F. ;
Dhert, W. J. A. ;
Malda, J. .
CARTILAGE, 2014, 5 (04) :221-230
[5]   Extracellular matrix scaffolds for cartilage and bone regeneration [J].
Benders, Kim E. M. ;
van Weeren, P. Rene ;
Badylak, Stephen F. ;
Saris, Daniel B. F. ;
Dhert, Wouter J. A. ;
Malda, Jos .
TRENDS IN BIOTECHNOLOGY, 2013, 31 (03) :169-176
[6]   Covalent attachment of a three-dimensionally printed thermoplast to a gelatin hydrogel for mechanically enhanced cartilage constructs [J].
Boere, Kristel W. M. ;
Visser, Jetze ;
Seyednejad, Hajar ;
Rahimian, Sima ;
Gawlitta, Debby ;
van Steenbergen, Mies J. ;
Dhert, Wouter J. A. ;
Hennink, Wim E. ;
Vermonden, Tina ;
Malda, Jos .
ACTA BIOMATERIALIA, 2014, 10 (06) :2602-2611
[7]   α-Tricalcium phosphate: Synthesis, properties and biomedical applications [J].
Carrodeguas, R. G. ;
De Aza, S. .
ACTA BIOMATERIALIA, 2011, 7 (10) :3536-3546
[8]   An overview of tissue and whole organ decellularization processes [J].
Crapo, Peter M. ;
Gilbert, Thomas W. ;
Badylak, Stephen F. .
BIOMATERIALS, 2011, 32 (12) :3233-3243
[9]  
Gawlitta D, 2015, TISSUE ENG PT A, V21, P694, DOI [10.1089/ten.tea.2014.0117, 10.1089/ten.TEA.2014.0117]
[10]   Low temperature direct 3D printed bioceramics and biocomposites as drug release matrices [J].
Gbureck, Uwe ;
Vorndran, Elke ;
Mueller, Frank A. ;
Barralet, Jake E. .
JOURNAL OF CONTROLLED RELEASE, 2007, 122 (02) :173-180