电场通过EGFR/p38 MAPK/Akt通路引导HaCaT细胞迁移。

IF 4.1 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Current Issues in Molecular Biology Pub Date : 2024-12-31 DOI:10.3390/cimb47010016
Huajian Zhou, Shihao Zhang, Xiaoli Jin, Chunxian A, Peng Gong, Sanjun Zhao
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引用次数: 0

摘要

已有研究表明,内源性电场(EF)是引导细胞向创面中心迁移,促进创面愈合的重要机制,但其机制尚不清楚。在这项研究中,我们研究了电场引导人类角质细胞HaCaT细胞迁移的分子机制。结果表明,在电场作用下,HaCaT细胞向阳极迁移。EF中p38 MAPK和Akt的磷酸化水平明显升高。敲除p38 MAPK可明显抑制EFs下HaCaT细胞的定向迁移。SB203580抑制p38 MAPK抑制ef引导的细胞迁移。电场可能通过EGFR/p38 MAPK/Akt通路引导HaCaT细胞迁移。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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The Electric Field Guided HaCaT Cell Migration Through the EGFR/p38 MAPK/Akt Pathway.

Previous studies have shown that the endogenous electric field (EF) is an overriding cure in guiding cell migration toward the wound center to promote wound healing, but the mechanism underlying is unclear. In this study, we investigated the molecular mechanism of electric field-guided cell migration in human keratinocyte HaCaT cells. Our results showed that HaCaT cells migrate toward the anode under EFs. The phosphorylation levels of p38 MAPK and Akt were obviously elevated in the EF. Knocking down p38 MAPK obviously abolished directed migration of HaCaT cells under the EFs. Inhibiting p38 MAPK by SB203580 impaired the EF-guided cell migration. The electric field may guide HaCaT cell migration through the EGFR/p38 MAPK/Akt pathway.

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来源期刊
Current Issues in Molecular Biology
Current Issues in Molecular Biology 生物-生化研究方法
CiteScore
2.90
自引率
3.20%
发文量
380
审稿时长
>12 weeks
期刊介绍: Current Issues in Molecular Biology (CIMB) is a peer-reviewed journal publishing review articles and minireviews in all areas of molecular biology and microbiology. Submitted articles are subject to an Article Processing Charge (APC) and are open access immediately upon publication. All manuscripts undergo a peer-review process.
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