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提取物通过角质形成细胞中ERK1/2的磷酸化促进伤口愈合。

Extract Promotes Wound Healing through the Phosphorylation of ERK1/2 in Keratinocytes.

作者信息

Kim Minho, Kim Jae-Goo, Kim Ki-Young

机构信息

Graduate School of Biotechnology, Kyung Hee University, Yongin-si 446-701, Gyeonggi-do, Korea.

Department of Genetics and Biotechnology, College of Life Science, and Graduate School of Biotechnology, Kyung Hee University, Seocheon, Giheung, Yongin-si 446-701, Gyeonggi-do, Korea.

出版信息

Biomimetics (Basel). 2022 Oct 7;7(4):154. doi: 10.3390/biomimetics7040154.

Abstract

The proliferation of keratinocytes is one of the important steps in the wound-healing process, which is regulated by various signals. Prior studies have shown that extract has the ability to promote angiogenesis. Therefore, in this study, we tested the wound-healing efficacy of extract with respect to promoting keratinocyte proliferation. A total of 100 μg/mL of extract treatment improved 145.38% of keratinocyte proliferation compared with DMSO-treated control in an MTT assay and increased 238.2% of wound closure by re-epithelialization in an in vitro wound-healing assay. extract promoted ERK1/2 phosphorylation in western blot analysis and induced the expression of the c-fos and c-jun (AP-1 transcription factors), cyclins (cell cycle regulator), and growth factors CTGF and VEGF (stimulator of angiogenesis) in qRT-PCR analysis. An in vivo wound-healing assay showed that extract improved wound healing, and the significant difference in wound closure compared with DMSO-treated control was shown on days 6 and 7 with a mouse model. Taken together, we demonstrate that extract promotes the proliferation of keratinocytes by activating ERK1/2 and increasing the mRNA expression of c-fos, c-jun, CTGF, and VEGF. Therefore, we suggest extract as a new component for skin care and as a wound-healing substance.

摘要

角质形成细胞的增殖是伤口愈合过程中的重要步骤之一,其受多种信号调控。先前的研究表明,提取物具有促进血管生成的能力。因此,在本研究中,我们测试了提取物在促进角质形成细胞增殖方面的伤口愈合功效。在MTT试验中,与二甲基亚砜(DMSO)处理的对照组相比,总共100μg/mL的提取物处理使角质形成细胞增殖提高了145.38%;在体外伤口愈合试验中,通过再上皮化使伤口闭合增加了238.2%。蛋白质印迹分析显示提取物促进细胞外信号调节激酶1/2(ERK1/2)磷酸化,实时定量聚合酶链反应(qRT-PCR)分析表明提取物诱导了原癌基因c-fos和原癌基因c-jun(激活蛋白-1转录因子)、细胞周期蛋白(细胞周期调节因子)以及生长因子结缔组织生长因子(CTGF)和血管内皮生长因子(VEGF)(血管生成刺激因子)的表达。体内伤口愈合试验表明,提取物改善了伤口愈合情况,在小鼠模型中,与DMSO处理的对照组相比,在第6天和第7天伤口闭合存在显著差异。综上所述,我们证明提取物通过激活ERK1/2并增加c-fos、c-jun、CTGF和VEGF的mRNA表达来促进角质形成细胞的增殖。因此,我们建议将提取物作为皮肤护理的新成分和伤口愈合物质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbfc/9624328/27754d52acb8/biomimetics-07-00154-g001.jpg

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