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Hydrostatic pressure induces apoptosis of chondrocytes cultured in alginate beads
Author(s) -
Nakamura Shu,
Arai Yuji,
Takahashi Kenji A.,
Terauchi Ryu,
Ohashi Suzuyo,
Mazda Osam,
Imanishi Jiro,
Inoue Atsuo,
Tonomura Hitoshi,
Kubo Toshikazu
Publication year - 2006
Publication title -
journal of orthopaedic research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.041
H-Index - 155
eISSN - 1554-527X
pISSN - 0736-0266
DOI - 10.1002/jor.20077
Subject(s) - hydrostatic pressure , apoptosis , microbiology and biotechnology , hydrostatic equilibrium , chemistry , biophysics , biology , mechanics , biochemistry , physics , quantum mechanics
The purpose of this study was to investigate the influence of hydrostatic pressure (HP) on apoptosis and expression of heat‐shock protein 70 (HSP70) in chondrocytes cultured in alginate beads. Chondrocytes were isolated from the articular cartilage of rabbit joints and seeded in alginate beads. The beads in Group A were cultured for less than 24 h after being embedded with the chondrocytes, while those in Group B were cultured for 2 weeks. Both groups were exposed to HP of 10 or 50 MPa for 12 or 24 h. The beads in Groups A and B that were not exposed to HP were regarded as controls. Apoptotic cells induced by exposure to HP were quantified using the TUNEL method. Immunohistochemical analysis for HSP70 and in situ TUNEL analysis were also performed. Apoptotic chondrocytes were not observed in the control cells under atmospheric pressure, whereas apoptosis was observed in the beads in Group A, and the number of apoptotic cells increased as the duration and magnitude of HP increased. On the other hand, we observed no significant population of apoptotic cells in the beads in Group B. Chondrocytes expressing HSP70 were not TUNEL positive in the histological analysis. Excessively strong HP could evoke apoptosis when the extracellular matrix did not accumulate around the chondrocytes. HSP70 expression was related to occurrence of apoptosis that resulted from HP. These findings suggest a mechanism for the pathogenesis of cartilage degeneration in osteoarthritis. © 2006 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res