Tantalum trabecular metal - addition of human skeletal cells to enhance bone implant interface strength and clinical application
Tantalum trabecular metal - addition of human skeletal cells to enhance bone implant interface strength and clinical application
The osteo-regenerative properties of allograft have recently been enhanced by addition of autogenous human bone marrow stromal cells (HBMSCs). Limitations in the use of allograft have prompted the investigation of tantalum trabecular metal (TTM) as a potential alternative. TTM is already in widespread orthopaedic use, although in applications where there is poor initial stability, or when TTM is used in conjunction with bone grafting, initial implant loading may need to be limited. The aim of this study was to evaluate the osteo-regenerative potential of TTM with HBMSCs, in direct comparison to human allograft and autograft. HBMSCs were cultured on blocks of TTM, allograft or autograft in basal and osteogenic media. Molecular profiling, confocal and scanning electron microscopy (SEM) and biochemical assays were used to characterize cell adherence, proliferation and phenotype. Mechanical testing was used to define the tensile characteristics of the constructs. HBMSCs displayed adherence and proliferation throughout TTM, evidenced by immunocytochemistry and SEM, with significant cellular ingrowth and matrix production through TTM. In contrast to cells cultured with allograft, cell proliferation assays showed significantly higher activity with TTM (p < 0.001), although molecular profiling confirmed no significant difference in expression of osteogenic genes. In contrast to acellular constructs, mechanical testing of cell-TTM constructs showed enhanced tensile characteristics, which compared favourably to cell-allograft constructs. These studies demonstrated the ability of TTM to support HBMSC growth and osteogenic differentiation comparable to allograft. Thus, TTM represents an alternative to allograft for osteo-regenerative strategies, extending its clinical applications as a substitute for allograft. Copyright © 2012 John Wiley & Sons, Ltd.
Smith, J.O.
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Sengers, B. G.
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Aarvold, A.
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Tayton, E. R.
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Dunlop, D. G.
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Oreffo, R. O. C.
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sm, None
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4 June 2012
Smith, J.O.
022d973d-c710-43a2-9f36-ae3873d62665
Sengers, B. G.
d6b771b1-4ede-48c5-9644-fa86503941aa
Aarvold, A.
cdb23726-6d5e-444a-979a-71ca7af83e3f
Tayton, E. R.
7569fb3b-2e05-4530-9a3e-ccbf76414318
Dunlop, D. G.
5f8d8b5c-e516-48b8-831f-c6e5529a52cc
Oreffo, R. O. C.
ff9fff72-6855-4d0f-bfb2-311d0e8f3778
sm, None
435823c8-8344-4f98-a782-e359374719f0
Smith, J.O., Sengers, B. G., Aarvold, A., Tayton, E. R., Dunlop, D. G., Oreffo, R. O. C. and sm, None
(2012)
Tantalum trabecular metal - addition of human skeletal cells to enhance bone implant interface strength and clinical application.
Journal of Tissue Engineering and Regenerative Medicine.
(doi:10.1002/term.1525).
(PMID:22674820)
Abstract
The osteo-regenerative properties of allograft have recently been enhanced by addition of autogenous human bone marrow stromal cells (HBMSCs). Limitations in the use of allograft have prompted the investigation of tantalum trabecular metal (TTM) as a potential alternative. TTM is already in widespread orthopaedic use, although in applications where there is poor initial stability, or when TTM is used in conjunction with bone grafting, initial implant loading may need to be limited. The aim of this study was to evaluate the osteo-regenerative potential of TTM with HBMSCs, in direct comparison to human allograft and autograft. HBMSCs were cultured on blocks of TTM, allograft or autograft in basal and osteogenic media. Molecular profiling, confocal and scanning electron microscopy (SEM) and biochemical assays were used to characterize cell adherence, proliferation and phenotype. Mechanical testing was used to define the tensile characteristics of the constructs. HBMSCs displayed adherence and proliferation throughout TTM, evidenced by immunocytochemistry and SEM, with significant cellular ingrowth and matrix production through TTM. In contrast to cells cultured with allograft, cell proliferation assays showed significantly higher activity with TTM (p < 0.001), although molecular profiling confirmed no significant difference in expression of osteogenic genes. In contrast to acellular constructs, mechanical testing of cell-TTM constructs showed enhanced tensile characteristics, which compared favourably to cell-allograft constructs. These studies demonstrated the ability of TTM to support HBMSC growth and osteogenic differentiation comparable to allograft. Thus, TTM represents an alternative to allograft for osteo-regenerative strategies, extending its clinical applications as a substitute for allograft. Copyright © 2012 John Wiley & Sons, Ltd.
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Published date: 4 June 2012
Organisations:
Human Development & Health
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Local EPrints ID: 345798
URI: http://eprints.soton.ac.uk/id/eprint/345798
ISSN: 1932-6254
PURE UUID: 9cb88963-b739-495a-804a-4902f6499ebf
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Date deposited: 04 Dec 2012 14:45
Last modified: 15 Mar 2024 03:26
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Author:
J.O. Smith
Author:
A. Aarvold
Author:
E. R. Tayton
Author:
D. G. Dunlop
Author:
None sm
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