A possible mechanism in DHEA-mediated protection against osteoarthritis

作者：Li, Wei-jun; Tang, Lu-ping; Xiong, Yan; Chen, Wei-ping; Zhou, Xin-die; Ding, Qian-hai; Wu, Li-dong^*

来源：Steroids, 2014, 89: 20-26.

DOI：10.1016/j.steroids.2014.07.011

• Dehydroepiandrosterone
• beta-Catenin
• Dickkopf1
• Osteoarthritis
• Chondrocyte
• Matrix metalloproteinase

Dehydroepiandrosterone (DHEA) and its ester form, DHEA-S, are the most abundant steroids in human plasma. Our previous studies showed that DHEA protects against osteoarthritis (OA). The aim of this paper was to explore the possible mechanisms that underlie DHEA-mediated protection against OA. We tested the expression of beta-catenin, it was increased significantly in OA. Rabbit cartilage was treated with various concentrations of DHEA in both IL-1 beta-induced rabbit chondrocytes and in rabbit cartilage from the anterior cruciate ligament transaction-induced OA model. We found DHEA decreased the expression of beta-catenin. Then we further activated Wnt/beta-catenin signaling by beta-catenin transfection and inactivated it by the inhibitor Dickkopf1 in chondrocytes to reveal its role in the pathogenesis of OA. It turns out the protective effect of DHEA was significantly decreased when Wnt/beta-catenin signaling was activated, while inactivating Wnt/beta-catenin signaling enhanced the effects of DHEA. Therefore, we hypothesize that DHEA probably exerted its chondroprotective effect by regulating Wnt/beta-catenin signaling. Our findings demonstrate the critical role of Wnt/beta-catenin signaling in DHEA-mediated protection against OA.

• 出版日期2014-11
• 单位浙江大学