Department of Prosthodontics, Harvard School of Dental Medicine, Boston, Massachusetts.
Department of Developmental Biology, Harvard School of Dental Medicine, Boston, Massachusetts; Faculty of Medicine, Harvard Medical School, Boston, Massachusetts.
Am J Pathol. 2016 Nov;186(11):3000-3010. doi: 10.1016/j.ajpath.2016.06.023. Epub 2016 Sep 16.
Osteoarthritis (OA) is the most common form of arthritis disorders, but the identification of therapeutic targets to effectively prevent OA has been increasingly difficult. The goal of this investigation is to provide experimental evidence that discoidin domain receptor 2 (DDR2) may be an ideal target for the development of disease-modifying OA drugs. Ddr2 was conditionally deleted from articular cartilage of adult mouse knee joints. Aggrecan-CreERT2;floxed Ddr2 mice, which were generated by crossing Aggrecan-CreERT2 mice with floxed Ddr2 mice, then received tamoxifen injections at the age of 8 weeks. The mice were then subjected to destabilization of the medial meniscus (DMM) surgery. At 8 and 16 weeks after DMM, mice were euthanized for the collection of knee joints. In a separate experiment, Aggrecan-CreERT2;floxed Ddr2 mice were subjected to DMM at the age of 10 weeks. The mice then received tamoxifen injections at 8 weeks after DMM. The mice were euthanized for the collection of knee joints at 16 weeks after DMM. The progressive process of articular cartilage degeneration was significantly delayed in the knee joints of Ddr2-deficient mice in comparison to their control littermates. Articular cartilage damage in the knee joints of the mice was associated with increased expression profiles of both Ddr2 and matrix metalloproteinase 13. These findings suggest that DDR2 may be an ideal target for the development of disease-modifying OA drugs.
骨关节炎(OA)是最常见的关节炎疾病,但识别有效的治疗靶点以预防 OA 已变得越来越困难。本研究的目的是提供实验证据,表明盘状结构域受体 2(DDR2)可能是开发治疗 OA 的药物的理想靶点。通过将 Aggrecan-CreERT2 小鼠与 floxed Ddr2 小鼠杂交,生成了条件性敲除成年小鼠膝关节关节软骨中 Ddr2 的 Aggrecan-CreERT2;floxed Ddr2 小鼠,然后在 8 周龄时给予他莫昔芬注射。然后对这些小鼠进行内侧半月板不稳定(DMM)手术。在 DMM 后 8 和 16 周,处死小鼠收集膝关节。在另一个实验中,Aggrecan-CreERT2;floxed Ddr2 小鼠在 10 周龄时进行 DMM。然后在 DMM 后 8 周给予他莫昔芬注射。在 DMM 后 16 周处死小鼠收集膝关节。与对照组相比,DDR2 缺失的小鼠膝关节中的关节软骨退化的进展过程明显延迟。DMM 后,小鼠膝关节中的关节软骨损伤与 Ddr2 和基质金属蛋白酶 13 的表达谱增加有关。这些发现表明,DDR2 可能是开发治疗 OA 的药物的理想靶点。