4.5 Article

Progressive Cell-Mediated Changes in Articular Cartilage and Bone in Mice Are Initiated by a Single Session of Controlled Cyclic Compressive Loading

期刊

JOURNAL OF ORTHOPAEDIC RESEARCH
卷 34, 期 11, 页码 1941-1949

出版社

WILEY
DOI: 10.1002/jor.23204

关键词

osteoarthritis; mouse; mechanical loading; bone resorption; chondrocytes

资金

  1. NIH [R01-AG028664, RC4-AR060546, R01-AG022021, R21-AR064034]
  2. NSF GRFP
  3. Clark Foundation
  4. Kirby Foundation

向作者/读者索取更多资源

We previously showed that repetitive cyclic loading of the mouse knee joint causes changes that recapitulate the features of osteoarthritis (OA) in humans. By applying a single loading session, we characterized the temporal progression of the structural and compositional changes in subchondral bone and articular cartilage. We applied loading during a single 5-minute session to the left tibia of adult (26-week-old) C57Bl/6 male mice at a peak load of 9.0N for 1,200 cycles. Knee joints were collected at times 0, 1, and 2 weeks after loading. The changes in articular cartilage and subchondral bone were analyzed by histology, immunohistochemistry (caspase-3 and cathepsin K), and microcomputed tomography. At time 0, no change was evident in chondrocyte viability or cartilage or subchondral bone integrity. However, cartilage pathology demonstrated by localized thinning and proteoglycan loss occurred at 1 and 2 weeks after the single session of loading. Transient cancellous bone loss was evident at 1 week, associated with increased osteoclast number. Bone loss was reversed to control levels at 2 weeks. We observed formation of fibrous and cartilaginous tissues at the joint margins at 1 and 2 weeks. Our findings demonstrate that a single session of noninvasive loading leads to the development of OA-like morphological and cellular alterations in articular cartilage and subchondral bone. The loss in subchondral trabecular bone mass and thickness returns to control levels at 2 weeks, whereas the cartilage thinning and proteoglycan loss persist. (C) 2016 Orthopaedic Research Society. Published by Wiley Periodicals, Inc.

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