胸腺基质淋巴细胞生成素
丝状蛋白
特应性皮炎
免疫学
表皮(动物学)
瘙痒的
表型
医学
调解人
角质形成细胞
细胞生物学
生物
癌症研究
细胞培养
遗传学
解剖
基因
作者
Marine Bernard,C. Acuña Carrasco,Léo Laoubi,B. Guiraud,Aurore Rozières,C. Goujon,Hélène Duplan,S. Bessou‐Touya,Jean‐François Nicolas,Marc Vocanson,M. Galliano
出处
期刊:
日期:2017-02-13
卷期号:242 (2): 234-245
被引量:61
摘要
2 polarization. Recent studies suggest that IL-1β contributes to the development of AD skin inflammation. Here, we have investigated the impact of IL-1β signalling on the epidermal homeostasis of both healthy subjects and AD patients [with functional filaggrin (FLG) alleles], with particular attention to TSLP production and keratinocyte differentiation. In healthy reconstructed human epidermis (RHE), IL-1β promoted (i) robust secretion of TSLP in an NF-κB-dependent manner and (ii) a significant decrease in the expression of filaggrin and other proteins of the epidermal differentiation complex. These effects were prevented by treatment of RHE with the anti-IL-1β mAb canakinumab and by the IL-1 receptor antagonist anakinra. Interestingly, RHE generated from AD donors behaved like that of healthy individuals and showed comparable responses to IL-1β signals. Collectively, our results suggest that IL-1β may be an early key mediator for the acquisition of an AD phenotype through induction of TSLP and alteration of the epidermal homeostasis. Copyright © 2017 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
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