## Abstract ## Objective To investigate the role of transforming growth factor Ξ² (TGFΞ²)/bone morphogenetic protein (BMP) superfamily members on accumulation of superficial zone protein (SZP) in articular chondrocytes and synoviocytes. ## Methods Chondrocytes and synoviocytes were isolated from a
Effects of mechanical stimuli on the synthesis of superficial zone protein in chondrocytes
β Scribed by T. Kamiya; K. Tanimoto; Y. Tanne; Y. Y. Lin; R. Kunimatsu; M. Yoshioka; N. Tanaka; E. Tanaka; K. Tanne
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 133 KB
- Volume
- 9999A
- Category
- Article
- ISSN
- 1549-3296
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β¦ Synopsis
Abstract
Superficial zone protein (SZP) has been demonstrated to contribute to the boundary lubrication in synovial joints. This study was designed to clarify the modulation of SZP expression by mechanical stress in articular chondrocytes. Cyclic tensile strains of 7 and 21% cell elongation were applied to cultured chondrocytes obtained from porcine mandibular condylar cartilage. The mRNA levels of SZP, ILβ1Ξ², and TGFβΞ²1 were examined by a quantitative realβtime PCR analysis. Protein level of SZP was examined by Western blotting. The SZP mRNA level was significantly upregulated after 12, 24, and 48 h by 7% elongation. Although SZP mRNA level was upregulated by 21% elongation after 12 h, it decreased to a lower level than the control after 48 h. The TGFβΞ²1 mRNA level exhibited an almost similar change to SZP. The ILβ1Ξ² mRNA level was not changed markedly by 7% elongation. However, the ILβ1Ξ² mRNA level was significantly increased by a 12βh application of 21% elongation. Western blot analysis revealed that the SZP expression was increased by 7% elongation, but decreased remarkably by 21% elongation. It is suggested from these findings that the SZP expression level in the chondrocytes is enhanced by optimal mechanical stimuli, but inhibited by excessive loading partly affected by TGFβΞ²1 and ILβ1Ξ², leading to the deterioration of joint lubrication. Β© 2009 Wiley Periodicals, Inc. J Biomed Mater Res, 2010
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