Comparative study between tissue-engineered periosteum and structural allograft in rabbit critical-sized radial defect model

被引:31
作者
Zhao, Lin [1 ]
Zhao, Junli [2 ]
Wang, Shuanke [1 ]
Wang, Junsheng [1 ]
Liu, Jia [1 ]
机构
[1] Lanzhou Univ, Dept Orthopaed Surg, Inst Orthopaed, Hosp 2, Lanzhou 730030, Peoples R China
[2] Lanzhou Univ, Dept Nephrol, Hosp 2, Lanzhou 730030, Peoples R China
基金
中国国家自然科学基金;
关键词
tissue engineering; periosteum; bone defect; allograft; MESENCHYMAL STEM-CELLS; SEGMENTAL BONE DEFECTS; SMALL-INTESTINAL SUBMUCOSA; ENDOTHELIAL GROWTH-FACTOR; EXTRACELLULAR-MATRIX; GRAFTS; VASCULARIZATION; OSTEOGENESIS; CHALLENGES; RESPONSES;
D O I
10.1002/jbm.b.31768
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The purpose of this study was to compare the efficacy of tissue-engineered periosteum (TEP) to allgeneic bone in repairing segmental bone defect. TEP was fabricated with osteoinduced rabbit bone marrow mesenchymal stem cells (MSCs) and porcine small intestinal submucosa (SIS). Allogrfats were cryopreserved radial segments of New Zealand Rabbits. Forty-eight radial critical-sized defects (CSD) were bilaterally produced in 24 rabbits. The defects were divided into three groups, group A, TEP implantation, group B, SIS implantation, and group C allograft. Bone defect reconstruction was kinetically analyzed at 4, 8, and 12 weeks by radiographic and histological scoring system. In group A, bone defects were radiographically and histologically healed with mature cortex and marrow cavity by 12 weeks, while none of the defects healed in group B. Group C showed a slow process of creeping substitution with lymphocyte infiltration. Statistical comparison confirmed that group A had a more efficient and rapid bone defect reparation as well as remodelling than Group B and C. In conclusion, TEP is superior to structural allograft in reconstruction of allogenic segmental bone defect. Pure SIS cannot guide bone regeneration in this rabbit model. (C) 2011 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater 978: 1-9, 2011.
引用
收藏
页码:1 / 9
页数:9
相关论文
共 35 条
[21]  
Ishikawa K, 1999, J BIOMED MATER RES, V47, P111, DOI 10.1002/(SICI)1097-4636(199911)47:2<111::AID-JBM1>3.3.CO
[22]  
2-S
[23]   Vascularization-The Conduit to Viable Engineered Tissues [J].
Kaully, Tamar ;
Kaufman-Francis, Keren ;
Lesman, Ayelet ;
Levenberg, Shulamit .
TISSUE ENGINEERING PART B-REVIEWS, 2009, 15 (02) :159-169
[24]   Bone tissue engineering in a critical size defect compared to ectopic implantations in the goat [J].
Kruyt, MC ;
Dhert, WJA ;
Yuan, HP ;
Wilson, CE ;
van Blitterswijk, CA ;
Verbout, AJ ;
de Bruijn, JD .
JOURNAL OF ORTHOPAEDIC RESEARCH, 2004, 22 (03) :544-551
[25]  
LANE JM, 1987, ORTHOP CLIN N AM, V18, P213
[26]   Mesenchymal stem cells inhibit and stimulate mixed lymphocyte cultures and mitogenic responses independently of the major histocompatibility complex [J].
Le Blanc, K ;
Tammik, L ;
Sundberg, B ;
Haynesworth, SE ;
Ringdén, O .
SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 2003, 57 (01) :11-20
[27]   The immunogenicity and immunomodulatory function of osteogenic cells differentiated from mesenchymal stem cells [J].
Liu, Hua ;
Kemeny, David Michael ;
Heng, Boon Chin ;
Ouyang, Hong Wei ;
Melendez, Alirio J. ;
Cao, Tong .
JOURNAL OF IMMUNOLOGY, 2006, 176 (05) :2864-2871
[28]   Preformed grafts of porcine small intestine submucosa (SIS) for bridging segmental bone defects [J].
Moore, DC ;
Pedrozo, HA ;
Crisco, JJ ;
Ehrlich, MG .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2004, 69A (02) :259-266
[29]   Comparison of immunological properties of bone marrow stromal cells and adipose tissue-derived stem cells before and after osteogenic differentiation in vitro [J].
Niemeyer, Philipp ;
Kornacker, Martin ;
Mehlhorn, Alexander ;
Seckinger, Anja ;
Vohrer, Jana ;
Schmal, Hagen ;
Kasten, Philip ;
Eckstein, Volker ;
Suedkamp, Norbert P. ;
Krause, Ulf .
TISSUE ENGINEERING, 2007, 13 (01) :111-121
[30]  
Parikh S N, 2002, J Postgrad Med, V48, P142