Division of Allergy, Immunology and Rheumatology Division of General Surgery, Buddhist Dalin Tzu Chi General Hospital, no. 2 Min-Sheng Road, Dalin Town, Chia-Yi, Taiwan.
Clin Exp Immunol. 2012 Apr;168(1):78-86. doi: 10.1111/j.1365-2249.2012.04563.x.
Abnormal Ca(2+) -mediated signalling contributes to the pathogenesis of rheumatoid arthritis (RA). However, the potential implication of calcium channel blocker in RA remained unknown. We hypothesized that nifedipine, an L-type calcium channel blocker, combined with a calcineurin inhibitor, could suppress T cell activation via targeting different level of the Ca(2+) signalling pathway. The percentage of activated T cells and the apoptotic rate of mononuclear cells (MNCs) was measured by flow cytometry. The MNC viability, cytokine production, cytosolic Ca(2+) level and activity of the nuclear factor of activated T cells (NFAT) were measured by enzyme-linked immunosorbent assay (ELISA). The NFAT-regulated gene expression, including interleukin (IL)-2, interferon (IFN)-γ and granulocyte-macrophage colony-stimulating factor (GM-CSF), was measured by real-time polymerase chain reaction (PCR). We found that the percentage of activated T cells in anti-CD3 + anti-CD28-activated MNC was higher in RA patients. High doses of nifedipine (50 µM) increased MNCs apoptosis, inhibited T cell activation and decreased T helper type 2 (Th1) (IFN-γ)/Th2 (IL-10) cytokine production in both groups. The Ca(2+) influx was lower in anti-CD3 + anti-CD28-activated MNC from RA patients than healthy volunteers and suppressed by nifedipine. When combined with a subtherapeutic dose (50 ng/ml) of cyclosporin, 1 µM nifedipine suppressed the percentage of activated T cells in both groups. Moreover, this combination suppressed more IFN-γ secretion and NFAT-regulated gene (GM-CSF and IFN-γ) expression in RA-MNCs than normal MNCs via decreasing the activity of NFATc1. In conclusion, we found that L-type Ca(2+) channel blockers and subtherapeutic doses of cyclosporin act additively to suppress the Ca(2+) -calcineurin-NFAT signalling pathway, leading to inhibition of T cell activity. We propose that this combination may become a potential treatment of RA.
异常的 Ca(2+)介导的信号转导导致类风湿关节炎 (RA) 的发病机制。然而,钙通道阻滞剂在 RA 中的潜在作用尚不清楚。我们假设硝苯地平,一种 L 型钙通道阻滞剂,与钙调神经磷酸酶抑制剂联合使用,可通过靶向 Ca(2+)信号通路的不同水平来抑制 T 细胞激活。通过流式细胞术测量激活的 T 细胞的百分比和单核细胞 (MNC) 的凋亡率。通过酶联免疫吸附试验 (ELISA) 测量 MNC 活力、细胞因子产生、细胞内 Ca(2+)水平和活化 T 细胞核因子 (NFAT) 的活性。通过实时聚合酶链反应 (PCR) 测量 NFAT 调节的基因表达,包括白细胞介素 (IL)-2、干扰素 (IFN)-γ 和粒细胞-巨噬细胞集落刺激因子 (GM-CSF)。我们发现 RA 患者抗 CD3+抗 CD28 激活的 MNC 中激活的 T 细胞百分比较高。高剂量硝苯地平 (50 µM) 增加了 MNC 凋亡,抑制了 T 细胞激活,并减少了两组中的 Th1(IFN-γ)/Th2(IL-10)细胞因子产生。RA 患者抗 CD3+抗 CD28 激活的 MNC 中的 Ca(2+)内流低于健康志愿者,并被硝苯地平抑制。当与亚治疗剂量 (50 ng/ml) 的环孢素联合使用时,1 µM 硝苯地平抑制了两组中激活的 T 细胞百分比。此外,这种组合通过降低 NFATc1 的活性,在 RA-MNC 中比在正常 MNC 中抑制更多的 IFN-γ 分泌和 NFAT 调节基因 (GM-CSF 和 IFN-γ) 表达。总之,我们发现 L 型钙通道阻滞剂和亚治疗剂量的环孢素通过抑制 T 细胞活性而协同作用于抑制 Ca(2+) -钙调神经磷酸酶-NFAT 信号通路。我们提出这种组合可能成为 RA 的一种潜在治疗方法。