Kou Xiao-Xing, Wang Xue-Dong, Li Chen-Shuang, Bi Rui-Yun, Meng Zhen, Li Bei, Zhou Yan-Heng, Gan Ye-Hua
Department of Orthodontics, 22 Zhongguancun Nandajie, Haidian District, Beijing 100081, PR China; Center for Craniofacial Stem Cell Research and Regeneration, 22 Zhongguancun Nandajie, Haidian District, Beijing 100081, PR China.
Department of Orthodontics, 22 Zhongguancun Nandajie, Haidian District, Beijing 100081, PR China.
J Steroid Biochem Mol Biol. 2014 Sep;143:444-50. doi: 10.1016/j.jsbmb.2014.07.002. Epub 2014 Jul 6.
Estrogen is involved in inflammation/pain of temporomandibular joint (TMJ), but the underlying mechanisms are largely unknown. Cadherin-11 plays an essential role in synovial inflammation. This study examined whether estrogen could potentiate cadherin-11 in synoviocytes and contribute to TMJ inflammatory pain. Female rats were ovariectomized, treated with increasing doses of 17β-estradiol for 10 days, and injected intra-articularly with complete Freund's adjuvant to induce TMJ inflammation. The expression of cadherin-11 in synovial membrane was evaluated. TMJ pain was blocked with intra-articular injection of anti-cadherin-11 antibody and evaluated by head withdrawal threshold. Primary TMJ synoviocytes were treated with estradiol and tumor necrosis factor (TNF)-α or blocked with anti-cadherin-11 antibody to assess the expression of cadherin-11, interleukin (IL)-6, cyclooxygenase 2 (COX-2), and inducible nitric oxide synthase (iNOS). We observed that estradiol potentiated the inflammation-induced expression of cadherin-11 in the synoviocytes of synovial membrane from inflamed TMJ. Estradiol induced cadherin-11 expression in a dose- and time-dependent manner in primary synoviocytes and further potentiated the induction of cadherin-11 by TNF-α in synoviocytes. Furthermore, an estrogen receptor antagonist or a NF-κB inhibitor partially blocked the effects of estradiol on cadherin-11 induction in the synovial membrane. Blocking cadherin-11 partially reversed the TMJ inflammatory pain and estradiol-potentiated proliferation of synovial lining cells accompanied with iNOS expression. In addition, blocking cadherin-11 reversed TNF-α-induced and estradiol-potentiated transcription of IL-6, COX-2, and iNOS in primary synoviocytes. These results suggest that estrogen aggravated TMJ inflammatory pain partially through cadherin-11-mediated release of proinflammatory cytokines and enzymes in the synoviocytes.
雌激素与颞下颌关节(TMJ)的炎症/疼痛有关,但其潜在机制尚不清楚。钙黏蛋白-11在滑膜炎症中起重要作用。本研究探讨雌激素是否能增强滑膜细胞中钙黏蛋白-11的表达并导致TMJ炎性疼痛。对雌性大鼠进行卵巢切除术,用递增剂量的17β-雌二醇治疗10天,并关节内注射完全弗氏佐剂以诱导TMJ炎症。评估滑膜中钙黏蛋白-11的表达。通过关节内注射抗钙黏蛋白-11抗体阻断TMJ疼痛,并通过甩头阈值进行评估。用雌二醇和肿瘤坏死因子(TNF)-α处理原代TMJ滑膜细胞,或用抗钙黏蛋白-11抗体阻断,以评估钙黏蛋白-11、白细胞介素(IL)-6、环氧化酶2(COX-2)和诱导型一氧化氮合酶(iNOS)的表达。我们观察到,雌二醇增强了炎症诱导的TMJ滑膜细胞中钙黏蛋白-11的表达。雌二醇在原代滑膜细胞中以剂量和时间依赖性方式诱导钙黏蛋白-11表达,并进一步增强TNF-α对滑膜细胞中钙黏蛋白-11的诱导作用。此外,雌激素受体拮抗剂或NF-κB抑制剂部分阻断了雌二醇对滑膜中钙黏蛋白-11诱导的作用。阻断钙黏蛋白-11可部分逆转TMJ炎性疼痛以及雌二醇增强的滑膜衬里细胞增殖,并伴有iNOS表达。此外,阻断钙黏蛋白-11可逆转TNF-α诱导的以及雌二醇增强的原代滑膜细胞中IL-6、COX-2和iNOS的转录。这些结果表明,雌激素部分通过钙黏蛋白-11介导的滑膜细胞中促炎细胞因子和酶的释放加重TMJ炎性疼痛。