MicroRNA-31 Can Positively Regulate the Proliferation, Differentiation and Migration of Keratinocytes.

Biomedicine Hub Pub Date : 2020-08-05 eCollection Date: 2020-05-01 DOI:10.1159/000508612
Fei Wang, Yuantao Gao, Yitong Yuan, Ruochen Du, Pengfei Li, Fang Liu, Ye Tian, Yali Wang, Ruxin Zhang, Bichun Zhao, Chunfang Wang
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引用次数: 7

Abstract

In the past decades, the key roles of most microRNA in dermatosis and skin development have been explored one after another. Among them, microRNA-31 (miR-31) has a prominent role in the regulation of keratinocytes. Numerous studies show that miR-31 can positively regulate the proliferation, differentiation and cell activity of keratinocytes via regulating the NF-κB, RAS/MAPK, Notch signaling pathways, and some cytokines. At present, the interaction between miR-31 and the NF-κB signaling pathway in keratinocytes is a hot research topic. The positive feedback loop formed by miR-31 and NF-κB signaling may bring new ideas for the prevention of psoriasis. The abnormal state of keratinocytes is usually the pathological basis of many skin and immune system diseases. Therefore, strengthening the ability to regulate keratinocytes may be a breakthrough for a variety of diseases. At the same time, miR-31's capacity to accelerate wound healing via positively regulating keratinocytes should be further investigated in the treatment of chronic ulcers and trauma.

MicroRNA-31可以正向调节角质形成细胞的增殖、分化和迁移。
在过去的几十年里,大多数microRNA在皮肤病和皮肤发育中的关键作用被陆续探索。其中,microRNA-31 (miR-31)在角化细胞的调控中具有突出作用。大量研究表明,miR-31可通过调节NF-κB、RAS/MAPK、Notch信号通路及部分细胞因子,正向调节角质形成细胞的增殖、分化和细胞活性。目前,miR-31与角质形成细胞NF-κB信号通路的相互作用是一个研究热点。miR-31与NF-κB信号通路形成的正反馈回路可能为银屑病的防治带来新的思路。角质形成细胞的异常状态通常是许多皮肤和免疫系统疾病的病理基础。因此,加强对角质形成细胞的调节能力可能是治疗多种疾病的突破口。同时,在慢性溃疡和创伤的治疗中,miR-31通过正向调节角质形成细胞加速伤口愈合的能力还有待进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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