首页> 外国专利> APPLICATION OF MICRORNA-210 INHIBITOR IN THE PREPARATION OF DRUGS FOR TREATING INFLAMMATORY SKIN DISEASES

APPLICATION OF MICRORNA-210 INHIBITOR IN THE PREPARATION OF DRUGS FOR TREATING INFLAMMATORY SKIN DISEASES

机译:MICRORNA-210抑制剂在制备治疗炎症性皮肤病的药物中的应用

摘要

Disclosed is application of a microRNA-210 inhibitor in the preparation of drugs for treating inflammatory skin diseases. The present inventor has demonstrated in a large number of experiments that in vitro inhibition of microRNA-210 expression can significantly enhance the expression of target gene STAT6 of microRNA-210, thereby inhibiting the proliferation of keratinocytes and the secretion of chemokine CCL20, further inhibiting chemotactic T cell migration towards a skin lesion part, and also inhibiting the differentiation of TH1 and TH17. MicroRNA-210 knockout and intradermal injection of a microRNA-210 inhibitor (cholesterol-modified antagomir-210) on a skin lesion specifically inhibit the expression of microRNA-210, so that skin inflammation in mice can be significantly inhibited and T cell immune imbalance is mitigated. The present invention provides a new pathophysiological mechanism for inflammatory skin diseases and provides a new strategy for preparing drugs for treating inflammatory skin diseases.
机译:公开了microRNA-210抑制剂在制备用于治疗炎性皮肤病的药物中的应用。本发明人在大量实验中证明,体外抑制microRNA-210的表达可以显着增强microRNA-210的靶基因STAT6的表达,从而抑制角质形成细胞的增殖和趋化因子CCL20的分泌,进一步抑制趋化性。 T细胞向皮肤病变部位迁移,并抑制T H 1和T H 17的分化。 MicroRNA-210基因敲除并在皮肤病变处皮内注射microRNA-210抑制剂(胆固醇修饰的antagomir-210)可特异性抑制microRNA-210的表达,因此可显着抑制小鼠皮肤炎症,并显着降低T细胞免疫失衡缓解。本发明为炎症性皮肤病提供了新的病理生理机制,为制备治疗炎症性皮肤病的药物提供了新的策略。

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