Decreased retinoid concentration and retinoid signalling pathways in human atopic dermatitis

维甲酸 视黄醇X受体α 维甲酸 视黄醇X受体β 视黄醇X受体γ 芬瑞替尼 视黄醇X受体 内分泌学 受体 化学 人体皮肤 维甲酸 内科学 生物 医学 生物化学 核受体 转录因子 基因 遗传学
作者
Johanna Mihály,Anat Gamlieli,Margitta Worm,Ralph Rühl
出处
期刊:Experimental Dermatology [Wiley]
卷期号:20 (4): 326-330 被引量:46
标识
DOI:10.1111/j.1600-0625.2010.01225.x
摘要

Abstract: Atopic dermatitis (AD) is one of the most common skin diseases. Various features present in AD like inflammation, reduced apoptosis, altered epidermal differentiation and hyperproliferation as well as permeability dysfunction are also regulated by retinoids. The aim of our study is to identify the retinoid signalling pathways and retinoid concentration profiles in AD skin. Human skin biopsies were obtained from healthy volunteers (HS) (n = 6) and patients with AD (n = 6), with both affected (AS) and non-affected (NAS) skin. The gene expression of retinoid receptors, retinoid-binding proteins and retinoid-metabolizing enzymes was investigated by QRT-PCR. Retinoid concentrations in serum and skin were measured via high performance liquid chromatography mass spectrometry–mass spectrometry. Our results show that the target gene expression of retinoid receptor regulated pathways is significantly decreased in AS and NAS of patients with AD. CYP26A1, transglutaminase 2 and retinoic acid receptor responder 1 decreased in NAS and AS in comparison with HS. The main retinoic acid synthesizing enzyme, retinal dehydrogenase 1, was significantly lower expressed in NAS (0.1%) and AS (1%) in patients with AD. Analysis of retinoid concentration in serum and skin showed comparable all-trans retinoic acid (ATRA) and retinol (ROL) concentrations from AD and healthy serum, but strongly reduced ATRA and ROL concentrations in affected and non-affected skin in comparison with healthy skin. Our data indicate that retinoid transport, synthesis, concentrations and signalling are strongly decreased in the affected but also in non-affected skin of patients with AD suggesting a general intrinsic influence on skin retinoid signalling pathway in patients with AD.
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