Abstract

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.

Highlights

  • Stability of the knee relies on the meniscus, a complex connective tissue with poor healing ability

  • It was demonstrated that both fibrin gel addition and optimized scaffold architecture effectively promote meniscal cell proliferation

  • When fibrin clots were tested in meniscal lesions in goats, it was found that adding fibrin did not improve the repair rate obtained by sutures alone, the organization of the repair tissue improved.[7]

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Summary

Introduction

Stability of the knee relies on the meniscus, a complex connective tissue with poor healing ability. Scaffold architecture and fibrin gels promote meniscal cell proliferation Collagen scaffold structure, isotropic or aligned, and fibrin gel addition were tested.

Results
Conclusion
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