Sakimoto Tohru, Ishimori Akiko
Department of Visual Sciences, Division of Ophthalmology, Nihon University School of Medicine, Tokyo, Japan.
Department of Visual Sciences, Division of Ophthalmology, Nihon University School of Medicine, Tokyo, Japan.
Exp Eye Res. 2016 Apr;145:110-117. doi: 10.1016/j.exer.2015.12.005. Epub 2015 Dec 12.
We evaluated an anti-inflammatory effect of topical administration of tofacitinib, janus kinase (JAK) blocker, on corneal inflammation. Topical instillation of either tofacitinib or PBS was applied after wounding BALB/c mice corneas with alkali burn. Topical instillation was performed until day 14 after injury and injured eye was analyzed. The vascularized area in the alkali burned cornea was significantly reduced in the tofacitinib group compared with that in the PBS group. The immunoreactivity of Gr-1, F4/80, IFN-γ, and phosphorylated STAT(signal transducer and activator of transcription)1 in corneal stroma was diminished significantly in the tofacitinib group. Using laser capture microdissection system and quantitative PCR array analysis, the expression levels of CXCL9, CXCL5, CCL7, CCL2, MMP(matrix metalloproteinase)-9, and STAT1 in corneal stroma were down-regulated in the tofacitinib group. In in vitro study, human fibroblast pretreated by IFN-γ showed phosphorylation of STAT1, and this phosphorylation was down-regulated by adding tofacitinib to the culture medium. These results indicate the topical application of JAK inhibitor causes down-regulation of JAK- or IFN-γ-related molecules. Therefore, we deduce that application of JAK inhibitor for topical instillation may contribute to the treatment of corneal inflammation.
我们评估了局部应用托法替布(一种 Janus 激酶(JAK)抑制剂)对角膜炎症的抗炎作用。在用碱烧伤 BALB/c 小鼠角膜后,局部滴注托法替布或 PBS。局部滴注持续至损伤后第 14 天,并对受伤眼睛进行分析。与 PBS 组相比,托法替布组碱烧伤角膜的血管化区域明显减少。托法替布组角膜基质中 Gr-1、F4/80、IFN-γ 和磷酸化 STAT(信号转导和转录激活因子)1 的免疫反应性显著降低。使用激光捕获显微切割系统和定量 PCR 阵列分析,托法替布组角膜基质中 CXCL9、CXCL5、CCL7、CCL2、基质金属蛋白酶(MMP)-9 和 STAT1 的表达水平下调。在体外研究中,经 IFN-γ 预处理的人成纤维细胞显示 STAT1 磷酸化,向培养基中添加托法替布可下调这种磷酸化。这些结果表明局部应用 JAK 抑制剂会导致 JAK 或 IFN-γ 相关分子的下调。因此,我们推断局部滴注 JAK 抑制剂可能有助于治疗角膜炎症。