Literature DB >> 18163475

Engineered cartilage generated by nasal chondrocytes is responsive to physical forces resembling joint loading.

C Candrian1, D Vonwil, A Barbero, E Bonacina, S Miot, J Farhadi, D Wirz, S Dickinson, A Hollander, M Jakob, Z Li, M Alini, M Heberer, I Martin.   

Abstract

OBJECTIVE: To determine whether engineered cartilage generated by nasal chondrocytes (ECN) is responsive to different regimens of loading associated with joint kinematics and previously shown to be stimulatory of engineered cartilage generated by articular chondrocytes (ECA).
METHODS: Human nasal and articular chondrocytes, harvested from 5 individuals, were expanded and cultured for 2 weeks into porous polymeric scaffolds. The resulting ECN and ECA were then maintained under static conditions or exposed to the following loading regimens: regimen 1, single application of cyclic deformation for 30 minutes; regimen 2, intermittent application of cyclic deformation for a total of 10 days, followed by static culture for 2 weeks; regimen 3, application of surface motion for a total of 10 days.
RESULTS: Prior to loading, ECN constructs contained significantly higher amounts of glycosaminoglycan (GAG) and type II collagen compared with ECA constructs. ECN responded to regimen 1 by increasing collagen and proteoglycan synthesis, to regimen 2 by increasing the accumulation of GAG and type II collagen as well as the dynamic modulus, and to regimen 3 by increasing the expression of superficial zone protein, at the messenger RNA level and the protein level, as well as the release of hyaluronan. ECA constructs were overall less responsive to all loading regimens, likely due to the lower extracellular matrix content.
CONCLUSION: Human ECN is responsive to physical forces resembling joint loading and can up-regulate molecules typically involved in joint lubrication. These findings should prompt future in vivo studies exploring the possibility of using nasal chondrocytes as a cell source for articular cartilage repair.

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Year:  2008        PMID: 18163475     DOI: 10.1002/art.23155

Source DB:  PubMed          Journal:  Arthritis Rheum        ISSN: 0004-3591


  23 in total

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Review 4.  Pro-chondrogenic effect of miR-221 and slug depletion in human MSCs.

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Review 5.  Emergence of scaffold-free approaches for tissue engineering musculoskeletal cartilages.

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7.  Response of human engineered cartilage based on articular or nasal chondrocytes to interleukin-1β and low oxygen.

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8.  Scaffold-based delivery of a clinically relevant anti-angiogenic drug promotes the formation of in vivo stable cartilage.

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9.  Prediction of cartilage compressive modulus using multiexponential analysis of T(2) relaxation data and support vector regression.

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10.  Human nasal cartilage ultrastructure: characteristics and comparison using scanning electron microscopy.

Authors:  Paul K Holden; Li-Huei Liaw; Brian J-F Wong
Journal:  Laryngoscope       Date:  2008-07       Impact factor: 3.325

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