Watanabe Hideaki, Kawaguchi Mio, Fujishima Sawa, Ogura Miyoko, Matsukura Satoshi, Takeuchi Hiroko, Ohba Motoi, Sueki Hirohiko, Kokubu Fumio, Hizawa Nobuyuki, Adachi Mitsuru, Huang Shau-Ku, Iijima Masafumi
Department of Dermatology, Showa University School of Medicine, Tokyo, Japan.
J Invest Dermatol. 2009 Mar;129(3):650-6. doi: 10.1038/jid.2008.294. Epub 2008 Oct 2.
IL-17F is known to be involved in many inflammatory diseases, but its role in skin diseases has not been fully examined. Because IL-8 is involved in many skin diseases such as psoriasis, we investigated the production of IL-8 in normal human epidermal keratinocytes (NHEKs) stimulated by IL-17F, tumor necrosis factor-alpha (TNF-alpha), IL-17A, and control using real-time PCR and ELISA. The results showed that IL-17F induced production of IL-8 in NHEKs in a time-dependent manner. Interestingly, the amounts of IL-8 stimulated by IL-17F were much higher than those stimulated by TNF-alpha or IL-17A. Next, we confirmed that selective mitogen-activated protein kinase kinase inhibitors significantly inhibited IL-17F-induced IL-8 production. Moreover, mouse skin intradermally injected with IL-17F expressed high level of IL-8 mRNA and induced ERK1/2 phosphorylation. Histological examination of mouse skin that was injected with IL-17F revealed marked neutrophilia in dermis and the infiltration was significantly inhibited by anti-IL-8 antibody. Finally, IL-17F expression in skin biopsy samples from psoriasis patients were examined by western blotting and ELISA. IL-17F was upregulated in lesional psoriatic skin compared with nonlesional skin. These results indicate that IL-17F may be involved in psoriasis via, in part, the activation of ERK1/2 and the induction of IL-8 in keratinocytes.
已知白细胞介素-17F(IL-17F)参与多种炎症性疾病,但它在皮肤病中的作用尚未得到充分研究。由于白细胞介素-8(IL-8)参与了许多皮肤病,如银屑病,我们使用实时定量聚合酶链反应(PCR)和酶联免疫吸附测定(ELISA),研究了IL-17F、肿瘤坏死因子-α(TNF-α)、IL-17A以及对照刺激正常人表皮角质形成细胞(NHEK)后IL-8的产生情况。结果显示,IL-17F以时间依赖性方式诱导NHEK产生IL-8。有趣的是,IL-17F刺激产生的IL-8量远高于TNF-α或IL-17A刺激产生的量。接下来,我们证实选择性丝裂原活化蛋白激酶激酶抑制剂可显著抑制IL-17F诱导的IL-8产生。此外,皮内注射IL-17F的小鼠皮肤表达高水平的IL-8信使核糖核酸(mRNA)并诱导细胞外信号调节激酶1/2(ERK1/2)磷酸化。对注射IL-17F的小鼠皮肤进行组织学检查发现真皮中有明显的嗜中性粒细胞增多,并且抗IL-8抗体可显著抑制这种浸润。最后,通过蛋白质免疫印迹法(western blotting)和ELISA检测银屑病患者皮肤活检样本中IL-17F的表达。与非皮损皮肤相比,IL-17F在银屑病皮损皮肤中上调。这些结果表明,IL-17F可能部分通过激活ERK1/2和诱导角质形成细胞产生IL-8而参与银屑病的发病过程。