Perspective on the Evolution of Cell-Based Bone Tissue Engineering Strategies

被引:34
作者
Jakob, M.
Saxer, F.
Scotti, C.
Schreiner, S.
Studer, P.
Scherberich, A.
Heberer, M.
Martin, I. [1 ]
机构
[1] Univ Basel Hosp, Inst Surg Res & Hosp Management, Dept Surg, CH-4031 Basel, Switzerland
关键词
Bioreactor systems; Bone regeneration; Cell-based bone graft substitutes; Developmental engineering; Intraoperative graft engineering; Stromal vascular fraction; Tissue engineering; HUMAN ADIPOSE-TISSUE; MARROW STROMAL CELLS; 3-DIMENSIONAL PERFUSION CULTURE; REAMER-IRRIGATOR-ASPIRATOR; MESENCHYMAL STEM-CELLS; DONOR SITE MORBIDITY; ILIAC CREST; MORPHOGENETIC PROTEINS; GRAFT SUBSTITUTES; ANTERIOR;
D O I
10.1159/000338362
中图分类号
R61 [外科手术学];
学科分类号
摘要
Despite the compelling clinical needs in enhancing bone regeneration and the potential offered by the field of tissue engineering, the adoption of cell-based bone graft substitutes in clinical practice is limited to date. In fact, no study has yet convincingly demonstrated reproducible clinical performance of tissue-engineered implants and at least equivalent cost-effectiveness compared to the current treatment standards. Here, we propose and discuss how tissue engineering strategies could be evolved towards more efficient solutions, depicting three different experimental paradigms: (i) bioreactor-based production; (ii) intraoperative manufacturing, and (iii) developmental engineering. The described approaches reflect the need to streamline graft manufacturing processes while maintaining the potency of osteoprogenitors and recapitulating the sequence of biological steps occurring during bone development, including vascularization. The need to combine the assessment of efficacy of the different strategies with the understanding of their mechanisms of action in the target regenerative processes is highlighted. This will be crucial to identify the necessary and sufficient set of signals that need to be delivered at the injury or defect site and should thus form the basis to define release criteria for reproducibly effective engineered bone graft substitutes. Copyright (c) 2012 S. Karger AG, Basel
引用
收藏
页码:1 / 7
页数:7
相关论文
共 48 条
[1]   Comparison of anterior and posterior iliac crest bone grafts in terms of harvest-site morbidity and functional outcomes [J].
Ahlmann, E ;
Patzakis, M ;
Roidis, N ;
Shepherd, L ;
Holtom, P .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 2002, 84A (05) :716-720
[2]   Molecular mechanisms controlling bone formation during fracture healing and distraction osteogenesis [J].
Ai-Aql, Z. S. ;
Alagl, A. S. ;
Graves, D. T. ;
Gerstenfeld, L. C. ;
Einhorn, T. A. .
JOURNAL OF DENTAL RESEARCH, 2008, 87 (02) :107-118
[3]   Complications of iliac crest bone graft harvesting [J].
Arrington, ED ;
Smith, WJ ;
Chambers, HG ;
Bucknell, AL ;
Davino, NA .
CLINICAL ORTHOPAEDICS AND RELATED RESEARCH, 1996, (329) :300-309
[4]   Osteogenic differentiation of noncultured immunoisolated bone marrow-derived CD105+ cells [J].
Aslan, Hadi ;
Zilberman, Yoram ;
Kandel, Leonid ;
Liebergall, Meir ;
Oskouian, Rod J. ;
Gazit, Dan ;
Gazit, Zulma .
STEM CELLS, 2006, 24 (07) :1728-1737
[5]   Proliferation kinetics and differentiation potential of ex vivo expanded human bone marrow stromal cells: Implications for their use in cell therapy [J].
Banfi, A ;
Muraglia, A ;
Dozin, B ;
Mastrogiacomo, M ;
Cancedda, R ;
Quarto, R .
EXPERIMENTAL HEMATOLOGY, 2000, 28 (06) :707-715
[6]  
Bates P., 2007, Basic Orthopaedic Sciences, P123
[7]   Arthroplasty of the lunate using bone marrow mesenchymal stromal cells [J].
Berner, Arne ;
Pfaller, Carola ;
Dienstknecht, Thomas ;
Zellner, Johannes ;
Mueller, Michael ;
Prantl, Lukas ;
Kujat, Richard ;
Englert, Carsten ;
Fuechtmeier, Bernd ;
Nerlich, Michael ;
Angele, Peter .
INTERNATIONAL ORTHOPAEDICS, 2011, 35 (03) :379-387
[8]   Biology of lumbar spine fusion and use of bone graft substitutes: Present, future, and next generation [J].
Boden, SD .
TISSUE ENGINEERING, 2000, 6 (04) :383-399
[9]   Three-dimensional perfusion culture of human bone marrow cells and generation of osteoinductive grafts [J].
Braccini, A ;
Wendt, D ;
Jaquiery, C ;
Jakob, M ;
Heberer, M ;
Kenins, L ;
Wodnar-Filipowicz, A ;
Quarto, R ;
Martin, I .
STEM CELLS, 2005, 23 (08) :1066-1072
[10]   The osteogenicity of implanted engineered bone constructs is related to the density of clonogenic bone marrow stromal cells [J].
Braccini, Alessandra ;
Wendt, David ;
Farhadi, Jian ;
Schaeren, Stefan ;
Heberer, Michael ;
Martin, Ivan .
JOURNAL OF TISSUE ENGINEERING AND REGENERATIVE MEDICINE, 2007, 1 (01) :60-65