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作 者:韩阳 张芯蕊 陈娟 刘文琪 李晓东[1] HAN Yang;ZHANG Xinrui;CHEN Juan;LIU Wenqi;LI Xiaodong(Central Hospital Affiliated To Shenyang Medical College,Shenyang 110024,China)
出 处:《中国麻风皮肤病杂志》2021年第1期8-12,共5页China Journal of Leprosy and Skin Diseases
基 金:沈阳医学院科技基金项目(编号:20196079)。
摘 要:目的:明确抑制树突细胞MMP-13基因对咪喹莫特诱导的小鼠银屑病样炎症模型的影响。方法:构建树突细胞MMP-13基因特异性敲除的小鼠模型(MMP-13 LOX/LOX),应用咪喹莫特诱导小鼠银屑病样皮损的发生。将小鼠分为野生型对照组、MMP-13 LOX/LOX对照组、咪喹莫特诱导的野生型实验组和咪喹莫特诱导的MMP-13 LOX/LOX实验组,分析不同组别小鼠皮损临床表现并记录PASI评分,检测各组小鼠皮损中IL-1β、IL-6、IL-23和IL-17A表达。结果:与咪喹莫特诱导的野生型实验组小鼠比较,咪喹莫特诱导的MMP-13 LOX/LOX实验组银屑病皮损表现相比更加温和,仅有轻度的棘层肥厚和真皮细胞浸润,皮损中IL-1β、IL-6表达下调,而IL-23和IL-17A表达无明显改变。结论:抑制树突细胞MMP-13基因可降低炎症因子IL-6、IL-1β的表达及减弱小鼠皮肤银屑病炎症反应。Objective:To determine the effect of inhibition of MMP-13 gene in dendritic cell on a mouse model of imiquimod-induced psoriasis.Methods:A mouse model of MMP-13 gene specific knockout in dendritic cells was constructed,and then,the psoriasis lesion was induced by imiquimod.Mice were divided into wild-type control group,MMP-13 LOX/LOX control group,wild-type imiquimod group,MMP-13 LOX/LOX imiquimod group.The clinical manifestations of skin lesions in each group and the psoriasis severity index(PASI)were assessed.The expressions of IL-1,IL-6,IL-23 and IL-17A in mice lesions were detected.Results:Compared with the wild-type imiquimod group,the lesions manifestation of the mice in MMP-13 LOX/LOX imiquimod group were milder,with only mild acanthosis and dermal cell infiltration.The expression level of IL-1 and IL-6 was lower and there was no significant difference in the expression level of IL-23 and IL-17A.Conclusion:Inhibition of MMP-13 gene of dendritic cells can decrease the level of IL-6 and IL-1β and inhibit the inflammation of psoriasis mouse model.
分 类 号:R758.63[医药卫生—皮肤病学与性病学]
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