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Current reconstructive approaches to large craniofacial skeletal defects are often complicated and challenging. Critical-sized defects are unable to heal via natural regenerative processes and require surgical intervention, traditionally involving autologous bone (mainly in the form of nonvascularized grafts) or alloplasts. Autologous bone grafts remain the gold standard of care in spite of the associated risk of donor site morbidity. Tissue engineering approaches represent a promising alternative that would serve to facilitate bone regeneration even in large craniofacial skeletal defects. This strategy has been tested in a myriad of iterations by utilizing a variety of osteoconductive scaffold materials, osteoblastic stem cells, as well as osteoinductive growth factors and small molecules. One of the major challenges facing tissue engineers is creating a scaffold fulfilling the properties necessary for controlled bone regeneration. These properties include osteoconduction, osteoinduction, biocompatibility, biodegradability, vascularization, and progenitor cell retention. This review will provide an overview of how optimization of the aforementioned scaffold parameters facilitates bone regenerative capabilities as well as a discussion of common osteoconductive scaffold materials.

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Publication history

Received: 31 July 2015
Accepted: 22 September 2015
Published: 02 October 2015
Issue date: March 2016

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© 2015 Chongqing Medical University.

Acknowledgements

Acknowledgements

The reported work was funded in part by the Chicago Biomedical Consortium with support from the Searle Funds at The Chicago Community Trust (RRR, GA), and a NIH/NIDCK Career Development Award (#1K08 DE020140-01; RRR). VT was a recipient of the Pritzker Summer Research Fellowship funded through a National Institutes of Health (NIH) T-35 training grant (NIDDK). ZC was a recipient of the Pritzker Research Fellowship. MKM was a recipient of Howard Hughes Medical Institute Medical Research Fellowship.

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This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

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