Kamekura Satoru, Kawasaki Yosuke, Hoshi Kazuto, Shimoaka Takashi, Chikuda Hirotaka, Maruyama Zenjiro, Komori Toshihisa, Sato Shingo, Takeda Shu, Karsenty Gerard, Nakamura Kozo, Chung Ung-il, Kawaguchi Hiroshi
Faculty of Medicine, University of Tokyo, Tokyo, Japan.
Arthritis Rheum. 2006 Aug;54(8):2462-70. doi: 10.1002/art.22041.
By producing instability in mouse knee joints, we attempted to determine the involvement of runt-related transcription factor 2 (RUNX-2), which is required for chondrocyte hypertrophy, in the development of osteoarthritis (OA).
An experimental mouse OA model was created by surgical transection of the medial collateral ligament and resection of the medial meniscus of the knee joints of heterozygous RUNX-2-deficient (Runx2+/-) mice and wild-type littermates. Cartilage destruction and osteophyte formation in the medial tibial cartilage were compared by histologic and radiographic analyses. Localization of type X collagen and matrix metalloproteinase 13 (MMP-13) was examined by immunohistochemistry. Localization of RUNX-2 was determined by X-Gal staining in heterozygous RUNX-2-deficient mice with the lacZ gene insertion at the Runx2-deletion site (Runx2+/lacZ). Messenger RNA levels of type X collagen, MMP-13, and RUNX-2 were examined by real-time reverse transcriptase-polymerase chain reaction analysis.
RUNX-2 was induced in the articular cartilage of wild-type mice at the early stage of OA, almost simultaneously with type X collagen but earlier than MMP-13. Runx2+/- and Runx2+/lacZ mice showed normal skeletal development and articular cartilage; however, after induction of knee joint instability, they exhibited decreased cartilage destruction and osteophyte formation, along with reduced type X collagen and MMP-13 expression, as compared with wild-type mice.
RUNX-2 contributes to the pathogenesis of OA through chondrocyte hypertrophy and matrix breakdown after the induction of joint instability.
通过使小鼠膝关节产生不稳定,我们试图确定软骨细胞肥大所需的 runt 相关转录因子 2(RUNX - 2)在骨关节炎(OA)发展中的作用。
通过手术切断内侧副韧带并切除杂合 RUNX - 2 缺陷(Runx2+/-)小鼠和野生型同窝小鼠膝关节的内侧半月板,建立实验性小鼠 OA 模型。通过组织学和影像学分析比较内侧胫骨软骨中的软骨破坏和骨赘形成。通过免疫组织化学检查 X 型胶原和基质金属蛋白酶 13(MMP - 13)的定位。在 Runx2 缺失位点插入 lacZ 基因的杂合 RUNX - 2 缺陷小鼠(Runx2+/lacZ)中,通过 X - Gal 染色确定 RUNX - 2 的定位。通过实时逆转录 - 聚合酶链反应分析检测 X 型胶原、MMP - 13 和 RUNX - 2 的信使核糖核酸水平。
在 OA 早期,野生型小鼠的关节软骨中诱导出 RUNX - 2,几乎与 X 型胶原同时出现,但早于 MMP - 13。Runx2+/-和 Runx2+/lacZ 小鼠显示正常的骨骼发育和关节软骨;然而,在诱导膝关节不稳定后,与野生型小鼠相比,它们表现出软骨破坏和骨赘形成减少,同时 X 型胶原和 MMP - 13 表达降低。
RUNX - 2 通过关节不稳定诱导后的软骨细胞肥大和基质分解,促进 OA 的发病机制。