Engineering tubular bone constructs

被引:25
作者
Chen, Fulin
Zhou, Yefang
Barnabas, Saey Tuan
Woodruff, Maria Ann
Hutmacher, Dietmar W. [1 ]
机构
[1] Natl Univ Singapore, Fac Engn, Div Bioengn, Singapore 117548, Singapore
[2] Natl Univ Singapore, Fac Engn, Dept Biol Sci, Singapore 117548, Singapore
[3] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Orthopaed Surg, Singapore 117548, Singapore
[4] Queensland Univ Technol, IHBI, Chair Regenerat Med, Brisbane, Qld, Australia
关键词
D O I
10.1016/j.jbiomech.2007.02.017
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Cell-sheet techniques have been proven effective in various soft tissue engineering applications. In this experiment, we investigated the feasibility of bone tissue engineering using a hybrid of mesenchymal stem cell (MSC) sheets and PLGA meshes. Porcine MSCs were Cultured to a thin layer of cell sheets via osteogenic induction. Tube-like long bones were constructed by wrapping the cell sheet on to PLGA meshes resulting in constructs which could be cultured in spinner flasks, prior to implantation in nude rats. Our results showed that the sheets were composed of viable cells and dense matrix with a thickness of about 80-120 mu m, mineral deposition was also observed in the sheet. In vitro cultures demonstrated calcified cartilage-like tissue formation and most PLGA meshes were absorbed during the 8-week Culture period. In vivo experiments revealed that dense mineralized tissue was formed in subcutaneous sites and the 8-week plants shared similar micro-CT characteristics with native bone. The neo tissue demonstrated histological markers for both bone and cartilage, indicating that the bone formation pathway in constructs was akin to endochondral ossification, with the residues of PLGA having an effect on the neo tissue organization and formation. These results indicate that cell-sheet approaches in combination with custom-shaped scaffolds have potential in producing bone tissue. (c) 2007 Published by Elsevier Ltd.
引用
收藏
页码:S73 / S79
页数:7
相关论文
共 21 条
[1]   DETERMINATION OF THE CAPACITY FOR PROLIFERATION AND DIFFERENTIATION OF OSTEOPROGENITOR CELLS IN THE PRESENCE AND ABSENCE OF DEXAMETHASONE [J].
BELLOWS, CG ;
HEERSCHE, JNM ;
AUBIN, JE .
DEVELOPMENTAL BIOLOGY, 1990, 140 (01) :132-138
[2]   Rabbit calvarial wound healing by means of seeded Caprotite® scaffolds [J].
Bidic, SMS ;
Calvert, JW ;
Marra, K ;
Kumta, P ;
Campbell, P ;
Mitchell, R ;
Wigginton, W ;
Hollinger, JO ;
Weiss, L ;
Mooney, MP .
JOURNAL OF DENTAL RESEARCH, 2003, 82 (02) :131-135
[3]   OSTEOLYTIC CHANGES ACCOMPANYING DEGRADATION OF ABSORBABLE FRACTURE FIXATION IMPLANTS [J].
BOSTMAN, OM .
JOURNAL OF BONE AND JOINT SURGERY-BRITISH VOLUME, 1991, 73 (04) :679-682
[4]   DIRECT COMPARISON OF A CULTURED COMPOSITE SKIN SUBSTITUTE CONTAINING HUMAN KERATINOCYTES AND FIBROBLASTS TO AN EPIDERMAL SHEET GRAFT CONTAINING HUMAN KERATINOCYTES ON ATHYMIC MICE [J].
COOPER, ML ;
ANDREE, C ;
HANSBROUGH, JF ;
ZAPATASIRVENT, RL ;
SPIELVOGEL, RL .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1993, 101 (06) :811-819
[5]   Adipose-derived adult stromal cells heal critical-size mouse calvarial defects [J].
Cowan, CM ;
Shi, YY ;
Aalami, OO ;
Chou, YF ;
Mari, C ;
Thomas, R ;
Quarto, N ;
Contag, CH ;
Wu, B ;
Longaker, MT .
NATURE BIOTECHNOLOGY, 2004, 22 (05) :560-567
[6]  
FRANCESCHI RT, 1994, J BONE MINER RES, V9, P843
[7]   Tissue engineering - Current challenges and expanding opportunities [J].
Griffith, LG ;
Naughton, G .
SCIENCE, 2002, 295 (5557) :1009-+
[8]   Scaffold design and fabrication technologies for engineering tissues - state of the art and future perspectives [J].
Hutmacher, DW .
JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, 2001, 12 (01) :107-124
[9]   A completely biological tissue-engineered human blood vessel [J].
L'Heureux, N ;
Pâquet, S ;
Labbé, R ;
Germain, L ;
Auger, FA .
FASEB JOURNAL, 1998, 12 (01) :47-56
[10]   Tissue engineering: The challenges ahead [J].
Langer, RS ;
Vacanti, JP .
SCIENTIFIC AMERICAN, 1999, 280 (04) :86-89