Scaffold architecture and fibrin gels promote meniscal cell proliferation

Stability of the knee relies on the meniscus, a complex connective tissue with poor healing ability. Current meniscal tissue engineering is inadequate, as the signals for increasing meniscal cell proliferation have not been established. In this study, collagen scaffold structure, isotro...

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Main Authors: K. M. Pawelec, S. M. Best, R. E. Cameron, R. J. Wardale
Format: Article
Language:English
Published: AIP Publishing LLC 2015-01-01
Series:APL Materials
Online Access:http://dx.doi.org/10.1063/1.4900885
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spelling doaj-69651cf5d1b64dffa380d2d15c6f60ad2020-11-25T02:26:20ZengAIP Publishing LLCAPL Materials2166-532X2015-01-0131014901014901-710.1063/1.4900885001595APMScaffold architecture and fibrin gels promote meniscal cell proliferationK. M. Pawelec0S. M. Best1R. E. Cameron2R. J. Wardale3Cambridge Centre for Medical Materials, Materials Science and Metallurgy Department, University of Cambridge, Cambridge CB3 0FS, United KingdomCambridge Centre for Medical Materials, Materials Science and Metallurgy Department, University of Cambridge, Cambridge CB3 0FS, United KingdomCambridge Centre for Medical Materials, Materials Science and Metallurgy Department, University of Cambridge, Cambridge CB3 0FS, United KingdomDivision of Trauma and Orthopaedic Surgery, Department of Surgery, University of Cambridge, Cambridge CB2 2QQ, United Kingdom Stability of the knee relies on the meniscus, a complex connective tissue with poor healing ability. Current meniscal tissue engineering is inadequate, as the signals for increasing meniscal cell proliferation have not been established. In this study, collagen scaffold structure, isotropic or aligned, and fibrin gel addition were tested. Metabolic activity was promoted by fibrin addition. Cellular proliferation, however, was significantly increased by both aligned architectures and fibrin addition. None of the constructs impaired collagen type I production or triggered adverse inflammatory responses. It was demonstrated that both fibrin gel addition and optimized scaffold architecture effectively promote meniscal cell proliferation. http://dx.doi.org/10.1063/1.4900885
collection DOAJ
language English
format Article
sources DOAJ
author K. M. Pawelec
S. M. Best
R. E. Cameron
R. J. Wardale
spellingShingle K. M. Pawelec
S. M. Best
R. E. Cameron
R. J. Wardale
Scaffold architecture and fibrin gels promote meniscal cell proliferation
APL Materials
author_facet K. M. Pawelec
S. M. Best
R. E. Cameron
R. J. Wardale
author_sort K. M. Pawelec
title Scaffold architecture and fibrin gels promote meniscal cell proliferation
title_short Scaffold architecture and fibrin gels promote meniscal cell proliferation
title_full Scaffold architecture and fibrin gels promote meniscal cell proliferation
title_fullStr Scaffold architecture and fibrin gels promote meniscal cell proliferation
title_full_unstemmed Scaffold architecture and fibrin gels promote meniscal cell proliferation
title_sort scaffold architecture and fibrin gels promote meniscal cell proliferation
publisher AIP Publishing LLC
series APL Materials
issn 2166-532X
publishDate 2015-01-01
description Stability of the knee relies on the meniscus, a complex connective tissue with poor healing ability. Current meniscal tissue engineering is inadequate, as the signals for increasing meniscal cell proliferation have not been established. In this study, collagen scaffold structure, isotropic or aligned, and fibrin gel addition were tested. Metabolic activity was promoted by fibrin addition. Cellular proliferation, however, was significantly increased by both aligned architectures and fibrin addition. None of the constructs impaired collagen type I production or triggered adverse inflammatory responses. It was demonstrated that both fibrin gel addition and optimized scaffold architecture effectively promote meniscal cell proliferation.
url http://dx.doi.org/10.1063/1.4900885
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