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Prinsepia utilis Royle polysaccharides promote skin barrier repair through the Claudin family

克洛丹 多糖 免疫印迹 经皮失水 表皮(动物学) 污渍 甲壳素 化学 分子生物学 生物 细胞生物学 紧密连接 生物化学 基因 解剖 角质层 壳聚糖 遗传学
作者
Bo Wang,Feifei Wang,Liping Qu,Hongyu Ma,Yuying Cheng,Xinlang Wu,Junxi Liu,Li He
出处
期刊:Skin Research and Technology [Wiley]
卷期号:30 (7) 被引量:3
标识
DOI:10.1111/srt.13848
摘要

Abstract Background Plant polysaccharides have various biological activities. However, few studies have been conducted on the skin barrier of Prinsepia utilis Royle polysaccharide extract (PURP). Materials and methods The proportions of polysaccharides, monosaccharides and proteins were determined by extracting polysaccharides from fruit meal using water. The healing rate was measured by cell scratch assays. SDS‐damaged reconstructed human epidermal models, an acetone–ether‐induced mouse model and an IL‐4‐induced cellular inflammation model were used to detect the effects of polysaccharides on the phenotype, HA, TEWL, and TEER, with further characterizations performed using QRT‐PCR, Western blotting, immunofluorescence (IF) assays. Results PURP contained 35.73% polysaccharides and 11.1% proteins. PURP promoted cell migration and increased skin thickness in a reconstructed human epidermis model. The TEWL significantly decreased, and the HA content significantly increased. PURP significantly increased the TEER and decreased the permeability of the SDS‐damaged reconstructed human epidermis model. Claudin‐3, Claudin‐4, and Claudin‐5 were significantly upregulated. IF and Western blot analysis revealed that the Claudin‐4 level significantly increased after treatment with PURP. Claudin‐1, Claudin‐3, Claudin‐4, and Claudin‐5 gene expression and IF and immunohistochemical staining were significantly increased in mice treated with acetone–ether. PURP promoted the expression of Claudin‐1, Claudin‐3, Claudin‐4, and Claudin‐5 after treatment with 100 ng/mL IL‐4. PURP also downregulated the expression of NO, IL6, TNFα and NFκB in Raw 264.7 cells and in a mouse model. Conclusion We hypothesize that PURP may repair the skin barrier by promoting the expression of the claudin family and can assist in skin therapy.
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