miR-34a partially reverses inhibition of CEES-exposed keratinocytes migration via ERK1/2 pathway
10.7644/j.issn.1674-9960.2014.11.002
- VernacularTitle:miR-34 a通过ERK1/2通路部分逆转CEES染毒对角质形成细胞迁移的抑制
- Author:
Feng YE
;
Jian WANG
;
Guorong DAN
;
Tao SHANGGUAN
;
Jiqing ZHAO
;
Yuanpeng ZHAO
;
Zhongmin ZOU
- Publication Type:Journal Article
- Keywords:
CEES;
HaCaT;
miR-34a;
cell migration;
ERK1/2
- From:
Military Medical Sciences
2014;(11):845-849
- CountryChina
- Language:Chinese
-
Abstract:
Objective To explore the effect of 2-chloroethyl ethyl sulfide(CEES) poisoning on keratinocyte migration and the regulatory role of microRNA(miR)-34a.Methods MTS was used to detect the viability of cells exposed to CEES in order to select an appropriate dose of CEES exposure in this in vitro model.The protein level of keratin 5 and keratin 10 was detected to assess cell differentiation status .Scratch assay was applied to evaluate cell migration ,and miR-34a silencing in keratinocytes was achieved by transfecting chemically synthesized miR-34a specific miRNA inhibitor.t-ERK1/2 and p-ERK1/2 levels closely related to cell migration were detected using Western blotting .Results An in vitro CEES exposure model of keratinocytes was established at the optimal concentration of 0.5 mmol/L CEES in the viability test , and this dose was chosen to evaluate cell migration changes .The migration of cells was significantly inhibited 24 h after CEES exposure , accompanied by no changes in morphology and keratin 5/10 levels.Silencing of miR-34a significantly increased the migration of cells exposed to CEES , which could be blocked by adding 5 μmol/L U0126 , an ERK1/2 phosphorylation selective inhibitor.Conclusion Silencing of miR-34a can significantly increase keratinocyte migration and partially reverse the inhibition of CEES-caused migration , which could be mediated by ERK 1/2 pathway activation .