口腔黏膜和皮肤伤口愈合中的不同炎症反应

T. Uchiyama, Xiaoyan Li, Kou Nakajima, Ayako Teranaka, Yi Liu, U. Bhawal, S. Hirayama
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引用次数: 0

摘要

伤口愈合是生物体生存的重要过程,但口腔黏膜与皮肤愈合能力的差异研究甚少。本研究的目的是评估口腔黏膜和皮肤的伤口愈合能力,并比较其愈合反应的差异。人牙龈成纤维细胞(HGF)和人皮肤成纤维细胞(HSF)在伤口愈合实验中被用来表征细胞迁移能力。在口腔黏膜和皮肤创面愈合小鼠模型中,采用RT-PCR检测创面周围组织中几种炎症标志物IL-1β、IL-6和IL-17的mRNA水平。采用免疫组化方法观察创面愈合后第3天口腔黏膜和皮肤的愈合能力,并比较IL-1β在口腔黏膜和创面周围皮肤组织中的表达水平。我们的研究结果表明,HSF细胞的细胞迁移速度比HGF细胞慢。体内实验表明,损伤诱导愈合口腔黏膜中IL-1β、IL-6和IL-17的表达高于愈合皮肤组织。口腔黏膜损伤的组织修复速度明显快于皮肤损伤。这些结果首次比较了口腔黏膜和皮肤对损伤反应的愈合能力差异,并提示不同损伤反应的愈合能力可能源于炎症标志物的表达差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Differential Inflammatory Responses in the Healing of Oral Mucosa and Skin Wounds
Wound healing is an essential process for organism survival, but differences in the healing ability between the oral mucosa and the skin have rarely been studied. The objective of this study was to evaluate the wound healing ability of oral mucosa and skin and to compare differences in their healing responses. Human gingival fibroblasts(HGF) and human skin fibroblasts(HSF)were used to characterize cell migration ability in wound healing assays. In oral mucosa and skin wound healing mouse models, mRNA levels of several inflammatory markers, IL-1β, IL-6 and IL-17, were examined in tissues collected around the wounds using RT-PCR. The healing ability of the oral mucosa as well as the skin was observed using immunohistochemistry at day 3 post-wound healing, and the expression level of IL-1β was also compared in oral mucosa and skin tissues collected around the wounds. Our findings showed that the cell migration of HSF cells was slower than HGF cells. In vivo experiments suggested that wounding induced a more significant up-regulation of IL-1β, IL-6 and IL-17 in healing oral mucosa compared with healing skin tissue. Tissue repair in oral mucosa wounds was more rap-id that in skin wounds. These results compared differences in the healing ability in response to injury in the oral mucosa and the skin for the first time and suggest that the healing ability of divergent reactions to injury may derive from expression differences among inflammatory markers.
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