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特定蛋白质在银屑病发病机制中的作用

The Role of Selected Proteins in the Pathogenesis of Psoriasis.

作者信息

Matwiejuk Mateusz, Kulczyńska-Przybik Agnieszka, Myśliwiec Hanna, Chabowski Adrian, Mroczko Barbara, Flisiak Iwona

机构信息

Department of Dermatology and Venereology, Medical University of Bialystok, 15-540 Bialystok, Poland.

Department of Neurodegeneration Diagnostics, Medical University of Bialystok, 15-269 Bialystok, Poland.

出版信息

Int J Mol Sci. 2025 Jul 4;26(13):6475. doi: 10.3390/ijms26136475.

DOI:10.3390/ijms26136475
PMID:40650250
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12250344/
Abstract

Psoriasis is a chronic, immune-mediated inflammatory skin disease with complex genetic, environmental, and immunological determinants. Beyond the skin, it affects multiple systems, including the joints and cardiovascular system. A hallmark of psoriasis is an overactivation of the innate and adaptive immune responses, leading to dysregulated cytokine signaling, altered keratinocyte function, and aberrant expression of structural and regulatory proteins. In recent years, growing attention has been given to the skin as a neuro-immuno-endocrine organ, with evidence showing the role of stress-related neuropeptides, UVB-induced immune modulation, and vitamin D signaling in the disease pathogenesis. This review highlights emerging evidence on key multifunctional proteins-elafin, chemerin, and NAMPT (visfatin)-that exert both pro- and anti-inflammatory actions. Although still underexplored, these molecules appear to contribute significantly to the psoriatic microenvironment by modulating inflammation, immunity, and skin barrier function. Their dual roles suggest complex interactions within the cutaneous immune-neuroendocrine network, positioning them as potential biomarkers or therapeutic targets in psoriasis. By integrating insights into classical and emerging mediators, this review aims to provide a comprehensive perspective on the evolving landscape of psoriasis pathophysiology.

摘要

银屑病是一种慢性、免疫介导的炎症性皮肤病,具有复杂的遗传、环境和免疫决定因素。除皮肤外,它还影响多个系统,包括关节和心血管系统。银屑病的一个标志是先天性和适应性免疫反应的过度激活,导致细胞因子信号失调、角质形成细胞功能改变以及结构和调节蛋白的异常表达。近年来,皮肤作为神经免疫内分泌器官受到越来越多的关注,有证据表明应激相关神经肽、紫外线B诱导的免疫调节以及维生素D信号在该疾病发病机制中的作用。本综述重点介绍了关键多功能蛋白——弹性蛋白、chemerin和烟酰胺磷酸核糖转移酶(内脂素)——的新证据,这些蛋白具有促炎和抗炎作用。尽管仍未得到充分研究,但这些分子似乎通过调节炎症、免疫和皮肤屏障功能,对银屑病微环境有显著贡献。它们的双重作用表明皮肤免疫神经内分泌网络内存在复杂的相互作用,使其成为银屑病潜在的生物标志物或治疗靶点。通过整合对经典和新出现介质的见解,本综述旨在提供一个关于银屑病病理生理学不断演变的全面观点。

相似文献

1
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本文引用的文献

1
Neuro-immuno-endocrinology of the skin: how environment regulates body homeostasis.皮肤的神经-免疫-内分泌学:环境如何调节身体稳态。
Nat Rev Endocrinol. 2025 Apr 22. doi: 10.1038/s41574-025-01107-x.
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Epidermal proteomics demonstrates Elafin as a psoriasis-specific biomarker and highlights increased anti-inflammatory activity around psoriatic plaques.表皮蛋白质组学表明弹性蛋白酶抑制剂是银屑病特异性生物标志物,并突出了银屑病斑块周围抗炎活性的增强。
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Biological Effects of CYP11A1-Derived Vitamin D and Lumisterol Metabolites in the Skin.CYP11A1 衍生的维生素 D 和路甾醇代谢物在皮肤中的生物学效应。
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The chemerin-CMKLR1 axis in keratinocytes impairs innate host defense against cutaneous Staphylococcus aureus infection.角质形成细胞中的 chemerin-CMKLR1 轴损害了先天宿主防御,导致皮肤金黄色葡萄球菌感染。
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Corticotropin-releasing hormone receptor-1 is increased in mast cells in psoriasis and actinic keratosis, but not markedly in keratinocyte skin carcinomas.促肾上腺皮质激素释放激素受体-1在银屑病和光化性角化病的肥大细胞中增加,但在角质形成细胞皮肤癌中没有明显增加。
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7
Chemerin Exacerbates Psoriasis by Stimulating Keratinocyte Proliferation and Cytokine Production.趋化素通过刺激角质形成细胞增殖和细胞因子产生加重银屑病。
Curr Med Sci. 2023 Apr;43(2):399-408. doi: 10.1007/s11596-023-2721-x. Epub 2023 Apr 5.
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Neuroendocrine signaling in the skin with a special focus on the epidermal neuropeptides.皮肤中的神经内分泌信号转导,特别关注表皮神经肽。
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Inverse correlation between the expression of AMPK/SIRT1 and NAMPT in psoriatic skin: A pilot study.银屑病皮肤中 AMPK/SIRT1 与 NAMPT 的表达呈负相关:一项初步研究。
Adv Med Sci. 2022 Sep;67(2):262-268. doi: 10.1016/j.advms.2022.07.001. Epub 2022 Jul 12.
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The Prevalence and Disease Characteristics of Generalized Pustular Psoriasis.泛发性脓疱型银屑病的患病率和疾病特征。
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