Jiangsu Key Laboratory of Molecular Biology for Skin Diseases and Sexually Transmitted Infections, Institute of Dermatology, Chinese Academy of Medical Sciences and Peking Union Medical College, Nanjing, Jiangsu, China; Department of Internal Medicine, Southern Illinois University School of Medicine, Springfield, Illinois, USA.
Department of Internal Medicine, Southern Illinois University School of Medicine, Springfield, Illinois, USA; Molecular Biology, Microbiology and Biochemistry, Southern Illinois University School of Medicine, Springfield, Illinois, USA.
J Invest Dermatol. 2019 Apr;139(4):859-867. doi: 10.1016/j.jid.2018.07.046. Epub 2018 Nov 2.
Psoriasis is a systemic inflammatory disease, associated with metabolic disorders, including high level of low-density lipoprotein. PCSK9, which promotes the degradation of low-density lipoprotein receptors and, therefore, the increased concentration of circulating low-density lipoprotein, is also involved in inflammation. This study aims to examine the role of PCSK9 in psoriasis and to investigate the potential of topically applying small interfering RNA targeting Pcsk9 as a psoriasis treatment. We investigated the expression of PCSK9 in lesions of psoriasis patients and imiquimod-induced psoriatic reactions in Pcsk9-knockout and Pcsk9 small interfering RNA-treated mice, and we also used cultured human keratinocytes to investigate the role of PCSK9 in regulating cell proliferation and apoptosis. We found that PCSK9 is overexpressed in psoriatic lesions and that suppressing Pcsk9 can decrease the inflammatory reaction induced by imiquimod treatment and inhibit hyperproliferation of keratinocytes. We also found that suppressing PCSK9 can significantly alter the cell cycle and induce apoptosis of human keratinocytes. Taken together, our findings indicate that PCSK9 plays an important role in psoriasis and may be a therapeutic target.
银屑病是一种系统性炎症性疾病,与代谢紊乱有关,包括低密度脂蛋白水平升高。PCSK9 可促进低密度脂蛋白受体的降解,从而导致循环中低密度脂蛋白浓度升高,同时它也参与炎症反应。本研究旨在探讨 PCSK9 在银屑病中的作用,并研究靶向 Pcsk9 的小干扰 RNA 局部应用作为银屑病治疗的潜力。我们研究了银屑病患者皮损和咪喹莫特诱导的 Pcsk9 敲除和 Pcsk9 小干扰 RNA 处理小鼠的 PCSK9 表达,并使用培养的人角质形成细胞研究 PCSK9 在调节细胞增殖和凋亡中的作用。我们发现 PCSK9 在银屑病皮损中过度表达,抑制 Pcsk9 可减轻咪喹莫特治疗引起的炎症反应,并抑制角质形成细胞的过度增殖。我们还发现抑制 PCSK9 可显著改变细胞周期并诱导人角质形成细胞凋亡。综上所述,我们的研究结果表明 PCSK9 在银屑病中发挥重要作用,可能是一个治疗靶点。