Lu Jian-Hua, Liu Yi-Qian, Deng Qiao-Wen, Peng Yu-Ping, Qiu Yi-Hua
Department of Physiology, School of Medicine and Co-Innovation Center of Neuroregeneration, Nantong University, 19 Qixiu Road, Nantong, Jiangsu 226001, China.
Biomed Res Int. 2015;2015:496759. doi: 10.1155/2015/496759. Epub 2015 Nov 29.
Human and murine lymphocytes express dopamine (DA) D2-like receptors including DRD2, DRD3, and DRD4. However, their roles in rheumatoid arthritis (RA) are less clear. Here we showed that lymphocyte DRD2 activation alleviates both imbalance of T-helper (Th)17/T-regulatory (Treg) cells and inflamed symptoms in a mouse arthritis model of RA. Collagen-induced arthritis (CIA) was prepared by intradermal injection of chicken collagen type II (CII) in tail base of DBA/1 mice or Drd2 (-/-) C57BL/6 mice. D2-like receptor agonist quinpirole downregulated expression of proinflammatory Th17-related cytokines interleukin- (IL-) 17 and IL-22 but further upregulated expression of anti-inflammatory Treg-related cytokines transforming growth factor- (TGF-) β and IL-10 in lymphocytes in vitro and in ankle joints in vivo in CIA mice. Quinpirole intraperitoneal administration reduced both clinical arthritis score and serum anti-CII IgG level in CIA mice. However, Drd2 (-/-) CIA mice manifested more severe limb inflammation and higher serum anti-CII IgG level and further upregulated IL-17 and IL-22 expression and downregulated TGF-β and IL-10 expression than wild-type CIA mice. In contrast, Drd1 (-/-) CIA mice did not alter limb inflammation or anti-CII IgG level compared with wild-type CIA mice. These results suggest that DRD2 activation is involved in alleviation of CIA symptoms by amelioration of Th17/Treg imbalance.
人类和小鼠淋巴细胞表达多巴胺(DA)D2样受体,包括DRD2、DRD3和DRD4。然而,它们在类风湿关节炎(RA)中的作用尚不清楚。在此我们表明,淋巴细胞DRD2激活可减轻RA小鼠关节炎模型中辅助性T(Th)17/调节性T(Treg)细胞的失衡及炎症症状。通过在DBA/1小鼠或Drd2(-/-)C57BL/6小鼠的尾基部皮内注射鸡II型胶原蛋白(CII)制备胶原诱导的关节炎(CIA)。D2样受体激动剂喹吡罗在体外淋巴细胞以及CIA小鼠体内踝关节中下调促炎Th17相关细胞因子白细胞介素(IL)-17和IL-22的表达,但进一步上调抗炎Treg相关细胞因子转化生长因子(TGF)-β和IL-10的表达。喹吡罗腹腔注射降低了CIA小鼠的临床关节炎评分和血清抗CII IgG水平。然而,与野生型CIA小鼠相比,Drd2(-/-)CIA小鼠表现出更严重的肢体炎症和更高的血清抗CII IgG水平,并且进一步上调IL-17和IL-22的表达,下调TGF-β和IL-10的表达。相比之下,与野生型CIA小鼠相比,Drd1(-/-)CIA小鼠的肢体炎症或抗CII IgG水平没有改变。这些结果表明,DRD2激活通过改善Th17/Treg失衡参与减轻CIA症状。