The Effects of Mucopolysaccharide Polysulfate on Steroid-Induced Tight Junction Barrier Dysfunction in Human Epidermal Keratinocytes and a 3D Skin Model

紧密连接 势垒函数 克洛丹 经皮失水 化学 人体皮肤 角质形成细胞 丙酸氯倍他索 特应性皮炎 角质层 医学 药理学 免疫学 银屑病 生物 细胞生物学 病理 体外 生物化学 遗传学
作者
Akira Koda,Yuko Ishii,Ayu Kashiwagi,Mika Fujikawa,Keisuke Kikuchi,Ryota Hashimoto,Yuhki Ueda,Takaaki Doi
出处
期刊:Skin Pharmacology and Physiology [S. Karger AG]
卷期号:36 (4): 186-194 被引量:1
标识
DOI:10.1159/000529962
摘要

The long-term use of topical corticosteroids (TCS) is associated with side effects such as skin atrophy and barrier deterioration. Moisturizers, such as mucopolysaccharide polysulfate (MPS), have been reported to prevent relapses in atopic dermatitis (AD) when used in combination with TCS. However, the mechanisms underlying the positive effects of MPS in combination with TCS in AD are poorly understood. In the present study, we investigated the effects of MPS in combination with clobetasol 17-propionate (CP) on tight junction (TJ) barrier function in human epidermal keratinocytes (HEKa) and 3D skin models.The expression of claudin-1, which is crucial for TJ barrier function in keratinocytes, and transepithelial electrical resistance (TEER) was measured in CP-treated human keratinocytes incubated with and without MPS. A TJ permeability assay, using Sulfo-NHS-Biotin as a tracer, was also conducted in a 3D skin model.CP reduced claudin-1 expression and TEER in human keratinocytes, whereas MPS inhibited these CP-induced effects. Moreover, MPS inhibited the increase in CP-induced TJ permeability in a 3D skin model.The present study demonstrated that MPS improved TJ barrier impairment induced by CP. The improvement of TJ barrier function may partially be responsible for the delayed relapse of AD induced by the combination of MPS and TCS.

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