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变应原受体及其在特应性皮炎中的伴侣。

Xenobiotic Receptors and Their Mates in Atopic Dermatitis.

机构信息

Department of Dermatology, Venereology and Allergology, Medical University of Innsbruck, 6020 Innsbruck, Austria.

出版信息

Int J Mol Sci. 2019 Aug 29;20(17):4234. doi: 10.3390/ijms20174234.

Abstract

Atopic dermatitis (AD) is the most common inflammatory skin disease worldwide. It is a chronic, relapsing and pruritic skin disorder which results from epidermal barrier abnormalities and immune dysregulation, both modulated by environmental factors. AD is strongly associated with asthma and allergic rhinitis in the so-called 'atopic march.' Xenobiotic receptors and their mates are ligand-activated transcription factors expressed in the skin where they control cellular detoxification pathways. Moreover, they regulate the expression of genes in pathways involved in AD in epithelial cells and immune cells. Activation or overexpression of xenobiotic receptors in the skin can be deleterious or beneficial, depending on context, ligand and activation duration. Moreover, their impact on skin might be amplified by crosstalk among xenobiotic receptors and their mates. Because they are activated by a broad range of endogenous molecules, drugs and pollutants owing to their promiscuous ligand affinity, they have recently crystalized the attention of researchers, including in dermatology and especially in the AD field. This review examines the putative roles of these receptors in AD by critically evaluating the conditions under which the proteins and their ligands have been studied. This information should provide new insights into AD pathogenesis and ways to develop new therapeutic interventions.

摘要

特应性皮炎(AD)是全球最常见的炎症性皮肤病。它是一种慢性、复发性和瘙痒性皮肤疾病,源于表皮屏障异常和免疫失调,两者均受环境因素的调节。AD 与哮喘和变应性鼻炎在所谓的“特应性进行曲”中密切相关。外源性生物受体及其伴侣是在皮肤中表达的配体激活转录因子,它们在那里控制细胞解毒途径。此外,它们调节上皮细胞和免疫细胞中参与 AD 的基因表达途径。外源性生物受体在皮肤中的激活或过度表达可能是有害的,也可能是有益的,这取决于环境、配体和激活持续时间。此外,由于它们与配体的广泛结合,它们与配体的伴侣之间的串扰可能会放大它们对皮肤的影响。由于它们具有广泛的内源性分子、药物和污染物的激活能力,由于其混杂的配体亲和力,它们最近引起了研究人员的关注,包括皮肤科,特别是 AD 领域。通过批判性地评估已研究过的蛋白质及其配体的条件,本综述检查了这些受体在 AD 中的潜在作用。这些信息应该为 AD 发病机制和开发新的治疗干预措施提供新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b04a/6747412/d930d5fb7dcb/ijms-20-04234-g001.jpg

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