Vascularization in Bone Tissue Engineering Constructs

被引:218
作者
Mercado-Pagan, Angel E. [1 ]
Stahl, Alexander M. [1 ,2 ]
Shanjani, Yaser [1 ]
Yang, Yunzhi [1 ,3 ]
机构
[1] Stanford Univ, Dept Orthoped Surg, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Mat Sci & Engn, Stanford, CA 94305 USA
关键词
Vascularized bone scaffolds; Vascular grafts; Osseointegration; Angiogenesis; Anastomosis; MESENCHYMAL STEM-CELLS; INDUCED MEMBRANE; DISTRACTION OSTEOGENESIS; EXTRACELLULAR-MATRIX; GROWTH-FACTOR; CHITOSAN GEL; GRAFT; SCAFFOLDS; BIOMATERIALS; INTEGRATION;
D O I
10.1007/s10439-015-1253-3
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Vascularization of large bone grafts is one of the main challenges of bone tissue engineering (BTE), and has held back the clinical translation of engineered bone constructs for two decades so far. The ultimate goal of vascularized BTE constructs is to provide a bone environment rich in functional vascular networks to achieve efficient osseointegration and accelerate restoration of function after implantation. To attain both structural and vascular integration of the grafts, a large number of biomaterials, cells, and biological cues have been evaluated. This review will present biological considerations for bone function restoration, contemporary approaches for clinical salvage of large bone defects and their limitations, state-of-the-art research on the development of vascularized bone constructs, and perspectives on evaluating and implementing novel BTE grafts in clinical practice. Success will depend on achieving full graft integration at multiple hierarchical levels, both between the individual graft components as well as between the implanted constructs and their surrounding host tissues. The paradigm of vascularized tissue constructs could not only revolutionize the progress of BTE, but could also be readily applied to other fields in regenerative medicine for the development of new innovative vascularized tissue designs.
引用
收藏
页码:718 / 729
页数:12
相关论文
共 124 条
[1]   Dynamics of bone marrow-derived endothelial progenitor cell/mesenchymal stem cell interaction in co-culture and its implications in angiogenesis [J].
Aguirre, A. ;
Planell, J. A. ;
Engel, E. .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2010, 400 (02) :284-291
[2]   Capillary vessel network integration by inserting a vascular pedicle enhances bone formation in tissue-engineered bone using interconnected porous hydroxyapatite ceramics [J].
Akita, S ;
Tamai, N ;
Myoui, A ;
Nishikawa, M ;
Kaito, T ;
Takaoka, K ;
Yoshikawa, H .
TISSUE ENGINEERING, 2004, 10 (5-6) :789-795
[3]   Osteoinduction, osteoconduction and osseointegration [J].
Albrektsson, T ;
Johansson, C .
EUROPEAN SPINE JOURNAL, 2001, 10 (Suppl 2) :S96-S101
[4]  
An YH., 2000, MECH TESTING BONE BO, P41
[5]   Cross-linked open-pore elastic hydrogels based on tropoelastin, elastin and high pressure CO2 [J].
Annabi, Nasim ;
Mithieux, Suzanne M. ;
Weiss, Anthony S. ;
Dehghani, Fariba .
BIOMATERIALS, 2010, 31 (07) :1655-1665
[6]  
ASTM, 2000, F 756-00
[7]   Geometric control of vascular networks to enhance engineered tissue integration and function [J].
Baranski, Jan D. ;
Chaturvedi, Ritika R. ;
Stevens, Kelly R. ;
Eyckmans, Jeroen ;
Carvalho, Brian ;
Solorzano, Ricardo D. ;
Yang, Michael T. ;
Miller, Jordan S. ;
Bhatia, Sangeeta N. ;
Chen, Christopher S. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2013, 110 (19) :7586-7591
[8]  
Bauer TW, 2000, CLIN ORTHOP RELAT R, P10
[9]   The role of pericytes in blood-vessel formation and maintenance [J].
Bergers, G ;
Song, S .
NEURO-ONCOLOGY, 2005, 7 (04) :452-464
[10]   Biomimetic tubular nanofiber mesh and platelet rich plasma-mediated delivery of BMP-7 for large bone defect regeneration [J].
Berner, A. ;
Boerckel, J. D. ;
Saifzadeh, S. ;
Steck, R. ;
Ren, J. ;
Vaquette, C. ;
Zhang, J. Qiyi ;
Nerlich, M. ;
Guldberg, R. E. ;
Hutmacher, D. W. ;
Woodruff, M. A. .
CELL AND TISSUE RESEARCH, 2012, 347 (03) :603-612