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IL-22 下调人角质形成细胞中的肽基精氨酸脱亚氨酶-1:在表皮屏障形成中添加 IL-22 之谜的另一个环节。

IL-22 Downregulates Peptidylarginine Deiminase-1 in Human Keratinocytes: Adding Another Piece to the IL-22 Puzzle in Epidermal Barrier Formation.

机构信息

Dermatology and Venereology Section, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden; Division of Clinical Microbiology, Department of Laboratory Medicine, Karolinska Institutet, Sweden.

Dermatology and Venereology Section, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden; Department of Microbiology, Tumor and Cell Biology, Science for Life Laboratory, Karolinska Institute, Stockholm, Sweden; The Program in Epithelial Biology, Stanford University School of Medicine, Stanford, California, USA.

出版信息

J Invest Dermatol. 2022 Feb;142(2):333-342.e6. doi: 10.1016/j.jid.2021.07.155. Epub 2021 Aug 2.

Abstract

Increased presence of IL-22 cells in the skin is a characteristic finding in skin barrier defects, such as psoriasis and atopic dermatitis. However, mechanistic insight into effects of IL-22 on epidermal functioning is yet to be elucidated. One crucial step during epidermal differentiation is deimination or citrullination. Here, we show reduced levels of peptidylarginine deiminase 1, an enzyme that converts peptidylarginine into citrulline in lesional psoriatic skin. IL-22 signaling through the IL-22 receptor complex was found to suppress expression of peptidylarginine deiminase 1 in epidermal keratinocytes. Subsequently, total peptidylarginine deiminase activity and extent of protein deimination in keratinocytes treated with IL-22 were reduced together with a significant decrease in deimination of keratin 1 and FLG, both important for epidermal differentiation. Vitamin D and acitretin partly restored the peptidylarginine deiminase 1 defect caused by IL-22. Collectively, we show that IL-22 downregulates deimination, thus identifying a potential target for treatment of skin barrier defects.

摘要

皮肤中 IL-22 细胞的增加是皮肤屏障缺陷的特征性发现,如银屑病和特应性皮炎。然而,IL-22 对表皮功能的影响的机制仍有待阐明。表皮分化过程中的一个关键步骤是脱亚氨基或瓜氨酸化。在这里,我们发现在病变的银屑病皮肤中,一种将肽精氨酸转化为瓜氨酸的酶——肽基精氨酸脱亚氨酶 1 的水平降低。IL-22 通过 IL-22 受体复合物的信号传导被发现可抑制表皮角质形成细胞中肽基精氨酸脱亚氨酶 1 的表达。随后,用 IL-22 处理的角质形成细胞中的总肽基精氨酸脱亚氨酶活性和蛋白质脱亚氨基程度降低,同时角蛋白 1 和 FLG 的脱亚氨基显著减少,这两者对表皮分化都很重要。维生素 D 和阿维 A 酯部分恢复了由 IL-22 引起的肽基精氨酸脱亚氨酶 1 缺陷。总的来说,我们表明 IL-22 下调脱亚氨基作用,从而确定了治疗皮肤屏障缺陷的潜在靶点。

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