Yu Xiaoyun, An Jingang, Hua Yunhui, Li Zihai, Yan Ning, Fan Weixin, Su Chuan
Department of Pathogen Biology & Immunology, Jiangsu Key Laboratory of Pathogen Biology, Nanjing Medical University, Nanjing, Jiangsu 210029, China; Department of Dermatovenereology, The Second Hospital of Nanjing, Nanjing, Jiangsu 210003, China.
Department of Dermatology, The Second Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi 710004, China.
Pathol Res Pract. 2017 Feb;213(2):89-97. doi: 10.1016/j.prp.2016.11.020. Epub 2016 Dec 19.
MicroRNAs (miRNAs) are currently emerged as important regulators in psoriasis. Psoriasis is characterized by hyperproliferation and impaired differentiation of keratinocytes in skin lesions. miR-194 is a well-known regulator of cell proliferation and differentiation. However, the role of miR-194 in psoriasis pathogenesis remains unclear. In this study we aimed to investigate the role of miR-194 in keratinocyte hyperproliferation and differentiation. We found that miR-194 was significantly downregulated in psoriasis lesional skin. Overexpression of miR-194 inhibited the proliferation and promoted the differentiation of primary human keratinocytes, whereas miR-194 suppression promoted the proliferation and inhibited their differentiation. Bioinformatic analysis predicted that the Grainyhead-like 2 (GRHL2) was a target gene of miR-194, which we further validated with a dual-luciferase reporter assay, real-time quantitative polymerase chain reaction (RT-qPCR), and Western blot analysis. The effect of miR-194 on cell proliferation and differentiation was significantly reversed by overexpression of GRHL2. Moreover, the expression of miR-194 and GRHL2 was inversely correlated in psoriasis lesional skin. Taken together, our results suggest that miR-194 inhibits the proliferation and promotes the differentiation of keratinocytes through targeting GRHL2. The downregulation of miR-194 expression may contribute to the pathogenesis of psoriasis and targeting miR-194 may represent a novel and potential therapeutic strategy for psoriasis.
微小RNA(miRNA)目前已成为银屑病的重要调节因子。银屑病的特征是皮肤病变中角质形成细胞过度增殖和分化受损。miR-194是一种众所周知的细胞增殖和分化调节因子。然而,miR-194在银屑病发病机制中的作用仍不清楚。在本研究中,我们旨在探讨miR-194在角质形成细胞过度增殖和分化中的作用。我们发现miR-194在银屑病皮损中显著下调。miR-194的过表达抑制了原代人角质形成细胞的增殖并促进其分化,而miR-194的抑制则促进了增殖并抑制了它们的分化。生物信息学分析预测颗粒头样2(GRHL2)是miR-194的靶基因,我们通过双荧光素酶报告基因检测、实时定量聚合酶链反应(RT-qPCR)和蛋白质印迹分析进一步验证了这一点。GRHL2的过表达显著逆转了miR-194对细胞增殖和分化的影响。此外,在银屑病皮损中,miR-194和GRHL2的表达呈负相关。综上所述,我们的结果表明miR-194通过靶向GRHL2抑制角质形成细胞的增殖并促进其分化。miR-194表达的下调可能有助于银屑病的发病机制,靶向miR-194可能代表一种新的潜在银屑病治疗策略。