Comparison of mouse and human ankles and establishment of mouse ankle osteoarthritis models by surgically-induced instability

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• 作者：S.H. Chang^&dagger ; ; ^{s5chang@yahoo.co.jp" class="auth_mail" title="E-mail the corresponding author} ; T. Yasui^&dagger ; ; ^{yasui.tokyo@gmail.com" class="auth_mail" title="E-mail the corresponding author} ; S. Taketomi^&dagger ; ; ^{TAKETOMIS-ORT@h.u-tokyo.ac.jp" class="auth_mail" title="E-mail the corresponding author} ; T. Matsumoto^&dagger ; ; ^{matumot-tky@umin.ac.jp" class="auth_mail" title="E-mail the corresponding author} ; J.R. Kim-Kaneyama^&Dagger ; ; ^{shuri@pharm.showa-u.ac.jp" class="auth_mail" title="E-mail the corresponding author} ; T. Omiya^&dagger ; ; ^{oomiya9ort@yahoo.co.jp" class="auth_mail" title="E-mail the corresponding author} ; Y. Hosaka^&dagger ; ; ^{hosakayort@gmail.com" class="auth_mail" title="E-mail the corresponding author} ; H. Inui^&dagger ; ; ^{hiroshi_inu0707@yahoo.co.jp" class="auth_mail" title="E-mail the corresponding author} ; Y. Omata^&dagger ; ; ^{grandbleu_1024@yahoo.co.jp" class="auth_mail" title="E-mail the corresponding author} ; R. Yamagami^&dagger ; ; ^{yamagami-tky@umin.ac.jp" class="auth_mail" title="E-mail the corresponding author} ; D. Mori^§ ; ; ^{Mori.Daisuke@technopro.com" class="auth_mail" title="E-mail the corresponding author} ; F. Yano^§ ; ; ^‖ ; ^{fumikoyano706@gmail.com" class="auth_mail" title="E-mail the corresponding author} ; U. Chung^‖ ; ^{uichung-tky@umin.ac.jp" class="auth_mail" title="E-mail the corresponding author} ; S. Tanaka^&dagger ; ; ^{tanakas-ort@h.u-tokyo.ac.jp" class="auth_mail" title="E-mail the corresponding author} ; T. Saito^&dagger ; ; ^§ ; ; ^{tasaitou-tky@umin.ac.jp" class="auth_mail" title="E-mail the corresponding author}
• 关键词：Osteoarthritis ; Chondrocytes ; Ankle ; Animal model
• 刊名：Osteoarthritis and Cartilage
• 出版年：2016
• 出版时间：April 2016
• 年：2016
• 卷：24
• 期：4
• 页码：688-697
• 全文大小：5202 K

文摘

Prevalence of ankle osteoarthritis (OA) is lower than that of knee OA, however, the molecular mechanisms underlying the difference remain unrevealed. In the present study, we developed mouse ankle OA models for use as tools to investigate pathophysiology of ankle OA and molecular characteristics of ankle cartilage.

Design

We anatomically and histologically examined ankle and knee joints of C57BL/6 mice, and compared them with human samples. We examined joints of 8-week-old and 25-month-old mice. For experimental models, we developed three different ankle OA models: a medial model, a lateral model, and a bilateral model, by resection of respective structures. OA severity was evaluated 8 weeks after the surgery by safranin O staining, and cartilage degradation in the medial model was sequentially examined.

Results

Anatomical and histological features of human and mouse ankle joints were comparable. Additionally, the mouse ankle joint was more resistant to cartilage degeneration with aging than the mouse knee joint. In the medial model, the tibiotalar joint was markedly affected while the subtalar joint was less degenerated. In the lateral model, the subtalar joint was mainly affected while the tibiotalar joint was less altered. In the bilateral model, both joints were markedly degenerated. In the time course of the medial model, TdT-mediated dUTP nick end labeling (TUNEL) staining and Adamts5 expression were enhanced at early and middle stages, while Mmp13 expression was gradually increased during the OA development.

Conclusion

Since human and mouse ankles are comparable, the present models will contribute to ankle OA pathophysiology and general cartilage research in future.