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ECa 233 通过 FAK/Akt、ERK 和 p38 MAPK 信号通路诱导角质形成细胞迁移。

Induction of keratinocyte migration by ECa 233 is mediated through FAK/Akt, ERK, and p38 MAPK signaling.

机构信息

Department of Pharmacology, Faculty of Science, Prince of Songkla University, Hat Yai, Songkhla, 90110, Thailand.

Faculty of Pharmaceutical Science, Burapha University, Chon Buri Campus, Chon Buri, 20131, Thailand.

出版信息

Phytother Res. 2018 Jul;32(7):1397-1403. doi: 10.1002/ptr.6075. Epub 2018 Mar 13.

Abstract

Centella asiatica is widely considered the most important medicinal plant for treating and relieving skin diseases. Recently developed standardized extract of Centella asiatica ECa 233 has demonstrated positive effects on wound healing of incision and burn wound in rats. However, knowledge associated with wound healing mechanism of ECa 233 was scare. Therefore, this study aimed to investigate the effect and underlying molecular mechanisms of ECa 233 on the migration of a human keratinocyte cell line (HaCaT) using scratch wound healing assay. Formation of filopodia, a key protein in cell migration as well as signaling pathways possibly involved were subsequently assessed. It was found that HaCaT cell migration was significantly enhanced by ECa 233 in a concentration- and time-dependent manner. The filopodia formations were accordingly increased in exposure to ECa 233 at concentrations of 0.1-100 μg/ml. Furthermore, ECa 233 was found to significantly upregulate the expression of Rac1 and RhoA and to induce phosphorylation of FAK and Akt as well as ERK and p38 MAPK. Taken all together, it is suggestive that ECa 233 induces cell migration and subsequently promotes wound healing activity, through the activation of FAK, Akt, and MAPK signaling pathways thereby supporting the role of ECa 233 to be further developed for the clinical treatment of wound.

摘要

积雪草被广泛认为是治疗和缓解皮肤病最重要的药用植物。最近开发的积雪草标准化提取物 ECa 233 已证明对大鼠切口和烧伤创面愈合有积极作用。然而,与 ECa 233 的伤口愈合机制相关的知识还很匮乏。因此,本研究旨在通过划痕愈合试验研究 ECa 233 对人角质形成细胞系 (HaCaT) 迁移的影响及其潜在的分子机制。随后评估了形成丝状伪足的情况,丝状伪足是细胞迁移的关键蛋白,以及可能涉及的信号通路。结果发现,ECa 233 以浓度和时间依赖的方式显著增强 HaCaT 细胞的迁移。在 0.1-100μg/ml 的浓度下暴露于 ECa 233,丝状伪足的形成相应增加。此外,还发现 ECa 233 显著上调 Rac1 和 RhoA 的表达,并诱导 FAK 和 Akt 以及 ERK 和 p38 MAPK 的磷酸化。综上所述,ECa 233 通过激活 FAK、Akt 和 MAPK 信号通路诱导细胞迁移,从而促进伤口愈合活性,这支持了将 ECa 233 进一步开发用于临床伤口治疗的作用。

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