Quantitative screening of engineered implants in a long bone defect model in rabbits

Tissue Engineering - Part C: Methods

Volumn 14, Issue 3, 2008, Pages 251-260

  Bakker, Astrid D ^a   Schrooten, Jan ^a   Van Cleynenbreugel, Tim ^a   Vanlauwe, Johan ^b   Luyten, Jan ^c   Schepers, Evert ^a   Dubruel, Peter ^d   Schacht, Etienne ^d   Lammens, Johan ^a,b   Luyten, Frank P ^a,b  

^a UNIVERSITY OF LEUVEN   (Belgium)

^b UNIVERSITY HOSPITALS LEUVEN   (Belgium)

^c FLEMISH INSTITUTE FOR TECHNOLOGICAL RESEARCH VITO   (Belgium)

^d GHENT UNIVERSITY   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

ABS RESINS; BIODEGRADABLE POLYMERS; HYDROXYAPATITE; POLYMER MATRIX COMPOSITES; SCAFFOLDS; TITANIUM;

BONE HEALING; CYLINDRICAL SCAFFOLDS; LONG BONE;

BONE;

BIOCERAMICS; HYDROXYAPATITE; TITANIUM;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BIODEGRADABILITY; BONE CONDUCTION; BONE DEFECT; BONE RADIOGRAPHY; CALLUS; COMPOSITE MATERIAL; CORTICAL BONE; FEMALE; FRACTURE HEALING; IMPLANT; LONG BONE; NONHUMAN; PERIOSTEUM; POROSITY; PRIORITY JOURNAL; RABBIT; TIBIA; TISSUE ENGINEERING;

ANIMALIA; ORYCTOLAGUS CUNICULUS;

EID: 51449109096     PISSN: 19373384     EISSN: 19373392     Source Type: Journal    
DOI: 10.1089/ten.tec.2008.0022     Document Type: Article

References (24)

1. Walkley, C.R., Olsen, G.H., Dworkin, S., Fabb, S.A., Swann, J., McArthur, G.A., Westmoreland, S.V., Chambon, P., Scadden, D.T., and Purton, L.E. A microenvironment-induced myeloproliferative syndrome caused by retinoic acid receptor gamma deficiency. Cell 129, 1097, 2007.
2. Engler, A.J., Sen, S., Sweeney, H.L., and Discher, D.E. Matrix elasticity directs stem cell lineage specification. Cell 126, 677, 2006.
3. Mauney, J.R., Volloch, V., and Kaplan, D.L. Role of adult mesenchymal stem cells in bone tissue engineering applications: current status and future prospects. Tissue Eng 11, 787, 2005.
4. Uebersax, L., Hagenmuler, H., Hofmann, S., Gruenblatt, E., Muler, R., Vunjak-Novakovic, G., Kaplan, D.L., Merkle, H.P., and Meinel, L. Effect of scaffold design on bone morphology in vitro. Tissue Eng 12, 3417, 2006.
5. Teixeira, A.I., Duckworth, J.K., and Hermanson, O. Getting the right stuff: controlling neural stem cell state and fate in vivo and in vitro with biomaterials. Cell Res 17, 56, 2007.
6. Hamada, K., Hirose, M., Yamashita, T., and Ohgushi, H. Spatial distribution of mineralized bone matrix produced by marrow mesenchymal stem cells in self-assembling peptide hydrogel scaffold. J Biomed Mater Res A. ISSN: 1552, 2007 (online).
7. Kim, M.S., Kim, S.K., Kim, S.H., Hyun, H., Khang, G., and Lee, H.B. In vivo osteogenic differentiation of rat bone marrow stromal cells in thermosensitive MPEG-PCL diblock copolymer gels. Tissue Eng 12, 2863, 2006.
8. Park, H., Temenoff, J.S., Tabata, Y., Caplan, A.I., and Mikos, A.G. Injectable biodegradable hydrogel composites for rabbit marrow mesenchymal stem cell and growth factor delivery for cartilage tissue engineering. Biomaterials 28, 3217, 2007.
9. Luyten, J., Mullens, S., Cooymans, J., de Wilde, A., and Thijs, I. New processing techniques of ceramic foams. Adv Eng Mat 5, 715, 2003.
10. Gorski, T., and Schacht, E.H. In situ crosslinkable poly (ortho)esters prepolymers for bone regeneration. 18th European Conference on Biomaterials, October 1-4, 2003, Stuttgart, Germany.
11. van Cleynenbreugel, T., Schrooten, J., van Oosterwyck, H., and Vander Sloten, J. Micro-CT based modelling and design of bone tissue engineering scaffolds. Med Biol Eng Comp 44, 517, 2006.
12. de Bari, C., Dell'Accio, F., and Luyten, F.P. Human periosteum-derived cells maintain phenotypic stability and chondrogenic potential throughout expansion regardless of donor age. Arthritis Rheum 44, 85, 2001.
13. Koshihara, Y., Hirano, M., Kawamura, M., Oda, H., and Higaki, S. Mineralization ability of cultured human osteoblast-like periosteal cells does not decline with aging. J Gerontol 46, B201, 1991.
14. Nakahara, H., Bruder, S.P., Goldberg, V.M., and Caplan, A.I. In vivo osteochondrogenic potential of cultured cells derived from the periosteum. Clin Orthop 259, 223, 1990.
15. Ito, Y., Fitzsimmons, J.S., Sanyal, A., Mello, M.A., Mukherjee, N., and O'Driscoll, S.W. Localization of chondrocyte precursors in periosteum. Osteoarthritis Cartilage 9, 215, 2001.
16. Stafford, H.J., Roberts, M.T., Oni, O.O., Hay, J., and Gregg, P. Localisation of boneforming cells during fracture healing by osteocalcin immunocytochemistry: an experimental study of the rabbit tibia. J Orthop Res 12, 29, 1994.
17. Ozaki, A., Tsunoda, M., Kinoshita, S., and Saura, R. Role of fracture hematoma and periosteum during fracture healing in rats: interaction of fracture hematoma and the periosteum in the initial step of the healing process. J Orthop Sci 5, 64, 2000.
18. Kojimoto, H., Yasui, N., Goto, T., Matsuda, S., and Shimomura, Y. Bone lengthening in rabbits by callus distraction: the role of periosteum and endosteum. J Bone Joint Surg Br 70, 543, 1988.
19. Hutmacher, D.W., and Sittinger, M. Periosteal cells in bone tissue engineering. Tissue Eng 9 (Suppl 1), S45, 2003.
20. Stevens, M.M., Marini, R.P., Schaefer, D., Aronson, J., Langer, R., and Shastri, V.P. In vivo engineering of organs: the bone bioreactor. Proc Natl Acad Sci USA 102, 11450, 2005.
21. Schantz, J.T., Hutmacher, D.W., Chim, H., Ng, K.W., Lim, T.C., and Teoh, S.H. Induction of ectopic bone formation by using human periosteal cells in combination with a novel scaffold technology. Cell Transplant 11, 25, 2002.
22. Takushima, A., Kitano, Y., and Harii, K. Osteogenic potential of cultured periosteal cells in a distracted bone gap in rabbits. J Surg Res 78, 68, 1998.
23. Eyckmans, J., and Luyten, F.P. Species specificity of ectopic bone formation using periosteum-derived mesenchymal progenitor cells. Tissue Eng 12, 2203, 2006.
24. Eyckmans, J., Bakker, A., and Luyten, F.P. Mode of action of ectopic bone formation induced by periosteum-derived progenitor cells. Proc. of the TERMIS-EU Meeting, 2006. Abstract no. 186.