3D skin model to investigate the early epidermal morphological psoriatic features

E. Donetti, G. Lombardo, F. B. Preis, L. Cornaghi, L. Pescitelli, F. Prignano
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引用次数: 3

Abstract

Epidermal cells, together with different molecules of the immunosystem, promote psoriasis, but several data concerning the early phases of this disease still lack. This study evaluated the early morphological features of psoriasis using an organotypic culture of normal human skin. Cellular proliferation, expressions of Toll-like receptors (TLR) 7 and 9, and keratin 17 were analysed by indirect immunofluorescence in normal human skin biopsies exposed to a cytokine mix strictly reproducing a psoriatic environment. After mix incubation, an early and progressive decrease of cell proliferation was detected. TLR9 was present in the granular layer of mix samples, while TLR7 was expressed throughout the entire epidermal compartment. K17 expression was evident after mix exposure. In conclusion, our results prove that a psoriatic microenvironment is able to induce pivotal morphological changes in our skin model, strongly suggesting that an early epidermal “psoriatic switch” can be reproduced for studying the epidermal homeostasis and innate immune response.
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三维皮肤模型研究银屑病早期表皮形态特征
表皮细胞与免疫系统的不同分子一起促进银屑病,但有关该疾病早期阶段的一些数据仍然缺乏。本研究使用正常人类皮肤的器官型培养来评估银屑病的早期形态特征。在暴露于严格再现银屑病环境的细胞因子混合物的正常人类皮肤活检中,通过间接免疫荧光分析细胞增殖、Toll样受体(TLR)7和9以及角蛋白17的表达。混合培养后,检测到细胞增殖的早期和渐进性下降。TLR9存在于混合样品的颗粒层中,而TLR7在整个表皮隔室中表达。混合暴露后K17表达明显。总之,我们的研究结果证明,银屑病微环境能够在我们的皮肤模型中诱导关键的形态学变化,这有力地表明,可以复制早期的表皮“银屑病开关”来研究表皮稳态和先天免疫反应。
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