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IL-6 通过激活 MEK/ERK/NF-κB 通路上调银屑病角质形成细胞中 LIM 结构域只有蛋白 4 的表达。

IL-6 Up-Regulates Expression of LIM-Domain Only Protein 4 in Psoriatic Keratinocytes through Activation of the MEK/ERK/NF-κB Pathway.

机构信息

Department of Immunology, School of Basic Medical Sciences, Anhui Medical University, Hefei, China; Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Anhui Medical University, Hefei, China.

Department of Dermatology, Anhui Medical University-Affiliated Provincial Hospital, Hefei, China.

出版信息

Am J Pathol. 2024 May;194(5):708-720. doi: 10.1016/j.ajpath.2024.01.014. Epub 2024 Feb 4.

DOI:10.1016/j.ajpath.2024.01.014
PMID:38320628
Abstract

Psoriasis is a chronic inflammatory skin disease characterized by the activation of keratinocytes and the infiltration of immune cells. Overexpression of the transcription factor LIM-domain only protein 4 (LMO4) promoted by IL-23 has critical roles in regulating the proliferation and differentiation of psoriatic keratinocytes. IL-6, an autocrine cytokine in psoriatic epidermis, is a key mediator of IL-23/T helper 17-driven cutaneous inflammation. However, little is known about how IL-6 regulates the up-regulation of LMO4 expression in psoriatic lesions. In this study, human immortalized keratinocyte cells, clinical biopsy specimens, and an animal model of psoriasis induced by imiquimod cream were used to investigate the role of IL-6 in the regulation of keratinocyte proliferation and differentiation. Psoriatic epidermis showed abnormal expression of IL-6 and LMO4. IL-6 up-regulated the expression of LMO4 and promoted keratinocyte proliferation and differentiation. Furthermore, in vitro and in vivo studies showed that IL-6 up-regulates LMO4 expression by activating the mitogen-activated extracellular signal-regulated kinase (MEK)/extracellular signal-regulated kinase (ERK)/NF-κB signaling pathway. These results suggest that IL-6 can activate the NF-κB signaling pathway, up-regulate the expression of LMO4, lead to abnormal proliferation and differentiation of keratinocytes, and promote the occurrence and development of psoriasis.

摘要

银屑病是一种慢性炎症性皮肤病,其特征在于角质形成细胞的激活和免疫细胞的浸润。白细胞介素-23(IL-23)促进转录因子 LIM 结构域只有蛋白 4(LMO4)的过表达在调节银屑病角质形成细胞的增殖和分化中起关键作用。IL-6 是银屑病表皮中的自分泌细胞因子,是 IL-23/T 辅助 17 驱动的皮肤炎症的关键介质。然而,对于 IL-6 如何调节银屑病病变中 LMO4 表达的上调知之甚少。在这项研究中,使用人永生化角质形成细胞、临床活检标本和咪喹莫特乳膏诱导的银屑病动物模型,研究了 IL-6 在调节角质形成细胞增殖和分化中的作用。银屑病表皮表现出 IL-6 和 LMO4 的异常表达。IL-6 上调 LMO4 的表达并促进角质形成细胞的增殖和分化。此外,体外和体内研究表明,IL-6 通过激活丝裂原活化细胞外信号调节激酶(MEK)/细胞外信号调节激酶(ERK)/核因子-κB(NF-κB)信号通路上调 LMO4 的表达。这些结果表明,IL-6 可以激活 NF-κB 信号通路,上调 LMO4 的表达,导致角质形成细胞异常增殖和分化,并促进银屑病的发生和发展。

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