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小窝蛋白-1作为银屑病的病理生理因素及靶点

Caveolin-1 as a pathophysiological factor and target in psoriasis.

作者信息

Kruglikov Ilja L, Scherer Philipp E

机构信息

Scientific Department, Wellcomet GmbH, Karlsruhe, Germany.

2Touchstone Diabetes Center, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390-8549 USA.

出版信息

NPJ Aging Mech Dis. 2019 Feb 5;5:4. doi: 10.1038/s41514-019-0034-x. eCollection 2019.

Abstract

Low expression of caveolin-1 (Cav-1) is typical in psoriatic lesions and overexpression of Cav-1 leads to a reduction of inflammation and suppression of epidermal hyperproliferation, thus ameliorating these two well-known hallmarks of psoriasis. At the same time, the interfacial layers of the white adipose tissue (WAT) adjacent to psoriatic lesions demonstrate much higher stiffness, which also points to a modification of Cav-1 expression in this tissue. These processes are connected with each other and regulated via exosomal exchange. Here we discuss the role of Cav-1 expression in inflammatory and hyperproliferative processes and analyze the ways to provide spatially different modulation of Cav-1 expression in the skin and WAT. Such modulation can be induced by different pharmacological and physical factors. These include application of mechanical stress and supra-physiological temperatures. Cav-1 should therefore be considered as an important target in treatment of psoriasis.

摘要

小窝蛋白-1(Cav-1)低表达在银屑病皮损中很典型,而Cav-1过表达会导致炎症减轻和表皮过度增殖受到抑制,从而改善银屑病这两个众所周知的特征。同时,与银屑病皮损相邻的白色脂肪组织(WAT)的界面层表现出更高的硬度,这也表明该组织中Cav-1表达发生了改变。这些过程相互关联并通过外泌体交换进行调节。在此,我们讨论Cav-1表达在炎症和过度增殖过程中的作用,并分析在皮肤和WAT中提供空间差异调节Cav-1表达的方法。这种调节可由不同的药理和物理因素诱导。这些因素包括施加机械应力和超生理温度。因此,Cav-1应被视为银屑病治疗的重要靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd03/6363785/b47bc4322a99/41514_2019_34_Fig1_HTML.jpg

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