Charles Institute of Dermatology, School of Medicine, University College Dublin, Dublin 4, Ireland.
Skin Biology and Pharmacology, Almirall R&D Centre, Sant Feliu de Llobregat, Barcelona, Spain.
Exp Dermatol. 2019 Nov;28(11):1298-1308. doi: 10.1111/exd.14030. Epub 2019 Sep 17.
Atopic dermatitis (AD) is a complex skin disease involving causative effects from both intrinsic and extrinsic sources. Murine models of the disease often fall short in one of these components and, as a result, do not fully encapsulate these disease mechanisms.
We aimed to determine whether the protease-activated receptor 2 over-expressor mouse (PAR2OE) with topical house dust mite (HDM) application is a more comprehensive and clinically representative AD model.
Following HDM extract application to PAR2OE mice and controls, AD clinical scoring, itching behaviour, skin morphology and structure, barrier function, immune cell infiltration and inflammatory markers were assessed. Skin morphology was analysed using haematoxylin and eosin staining, and barrier function was assessed by transepidermal water loss measurements. Immune infiltrate was characterised by histological and immunofluorescence staining. Finally, an assessment of AD-related gene expression was performed using quantitative RT-PCR.
PAR2OE mice treated with HDM displays all the characteristic clinical symptoms including erythema, dryness and oedema, skin morphology, itch and inflammation typically seen in patients with AD. There is a significant influx of mast cells (P < .01) and eosinophils (P < .0001) into the dermis of these mice. Furthermore, the PAR2OE + HDM mice exhibit similar expression patterns of key differentially expressed genes as seen in human AD.
The PAR2OE + HDM mouse presents with a classic AD pathophysiology and is a valuable model in terms of reproducibility and overall disease representation to study the condition and potential therapeutic approaches.
特应性皮炎(AD)是一种复杂的皮肤疾病,涉及内在和外在因素的致病作用。该疾病的小鼠模型在其中一个方面常常存在不足,因此不能完全包含这些疾病机制。
我们旨在确定过表达蛋白酶激活受体 2 的小鼠(PAR2OE)经局部屋尘螨(HDM)应用后是否是一种更全面和更具临床代表性的 AD 模型。
在对 PAR2OE 小鼠和对照小鼠应用 HDM 提取物后,评估 AD 临床评分、瘙痒行为、皮肤形态和结构、屏障功能、免疫细胞浸润和炎症标志物。采用苏木精和伊红染色分析皮肤形态,通过经表皮水分丢失测量评估屏障功能。通过组织学和免疫荧光染色来描述免疫浸润。最后,使用定量 RT-PCR 评估 AD 相关基因表达。
用 HDM 处理的 PAR2OE 小鼠表现出所有典型的临床症状,包括红斑、干燥和水肿、皮肤形态、瘙痒和炎症,这些症状通常见于 AD 患者。这些小鼠的真皮中有大量肥大细胞(P<.01)和嗜酸性粒细胞(P<.0001)浸润。此外,PAR2OE+HDM 小鼠表现出与人类 AD 中关键差异表达基因相似的表达模式。
PAR2OE+HDM 小鼠表现出经典的 AD 病理生理学,在可重复性和整体疾病表现方面是一种有价值的模型,可用于研究该疾病状况和潜在的治疗方法。