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首页|期刊导航|环境与职业医学|亚砷酸钠致人肝星状细胞活化中铁死亡相关基因SLC7A11和CDKN1A的DNA甲基化及表达变化

亚砷酸钠致人肝星状细胞活化中铁死亡相关基因SLC7A11和CDKN1A的DNA甲基化及表达变化

赵丽君 丁关鑫 黄菲 迪丽娜尔·亚尔麦麦提 吴顺华

环境与职业医学2023,Vol.40Issue(12):1403-1410,8.
环境与职业医学2023,Vol.40Issue(12):1403-1410,8.DOI:10.11836/JEOM23182

亚砷酸钠致人肝星状细胞活化中铁死亡相关基因SLC7A11和CDKN1A的DNA甲基化及表达变化

DNA methylation and expression changes of ferroptosis related genes SLC7A11 and CDKN1A in hu-man hepatic stellate cell activation induced by sodium arsenite

赵丽君 1丁关鑫 1黄菲 1迪丽娜尔·亚尔麦麦提 2吴顺华1

作者信息

  • 1. 新疆医科大学公共卫生学院劳动卫生与环境卫生学教研室,新疆 乌鲁木齐 830011
  • 2. 新疆医科大学公共卫生学院流行病与卫生统计学教研室,新疆 乌鲁木齐 830011
  • 折叠

摘要

Abstract

[Background]The accumulation of inorganic arsenic in the liver can lead to liver fibrosis.Solute carrier family 7 member 11(SLC7A11)and cyclin dependent kinase inhibitor 1A(CDKN1A)are ferroptosis related genes that are abnormally expressed in liver and fibrosis diseases,but their impacts on inorganic arsenic induced liver fibrosis has not been reported yet. [Objective]To explore the effect of different doses of sodium arsenite on the migration ability of human hepatic stellate(LX-2)cells and the changes in DNA methylation and expression of SLC7A11 and CDKN1A in LX-2 cell activation in-duced by sodium arsenite. [Methods]LX-2 cells were treated with different doses of sodium arsenite for 24 h.The experiment set up four groups:control group(0 μmol·L-1),low-dose group(5 μmol·L-1),medium-dose group(10 μmol·L-1),and high-dose group(15 μm·L-1).Possible morphological changes of LX-2 cells were observed under an inverted microscope in each group.Cell migration and movement were determined by cell scratch assay.Mitochondrial morphology was observed in the control and the high-dose groups under a transmission electron microscope(TEM).Fe2+ fluorescence intensity was detected with a FerroOrange fluorescence probe.Differentially methylated sites were screened using the Illumina 850 K methylation chip.Ferroptosis related markers(SLC7A11&CDKN1A)and hepatic stellate cell activation related markers[transforming growth factor-β1(TGF-β1)and collagen type Ⅲ(Collagen Ⅲ)]were detected by real-time fluorescence quantitative PCR and Western blot. [Results]With the increase of exposure dose,the cells retracted tentacles and gradually became round,and the healing of cell scratches gradually deteriorated.Destruction of mitochondrial membrane integrity and mitochondrial crista fracture in some cells were observed under a TEM in the high-dose group.Laser confocal microscopy showed that the fluorescence intensity of Fe2+ gradually increased with the increase of exposure dose.The results of methylation chip displayed that compared with the control group,high methylation was found in the high-dose group at the cg22659014 site in the promoter region of SLC7A11,and at the cg17964532 site in the promoter region of CDKN1A.With the increase of exposure dose,the mRNA and protein expression levels of SLC7A11 decreased(P<0.001);the CDKN1A mRNA expression level did not change significantly between groups(P>0.05),and its protein expression levels in the low-,medium-,and high-dose groups were higher than that in the control group(P<0.001).The TGF-β1 mRNA expression levels in the medium-and high-dose groups were higher than that in the control group(P<0.001),and its protein expression levels increased with the increase of exposure dose(P<0.001).The CollagenⅢ mRNA expression level increased with the increase of exposure dose(P<0.001),and its protein expression level was higher only in high-dose group than that in the control group(P<0.001). [Conclusion]Sodium arsenite exposure can weaken the migration ability of LX-2 cells,and the ferroptosis related genes SLC7A11 and CDKN1A are involved in the process of sodium arsenite-induced activation of LX-2 cells.

关键词

亚砷酸钠/人肝星状细胞/DNA甲基化/溶质载体家族7成员11/铁死亡

Key words

sodium arsenite/human hepatic stellate cell/DNA methylation/solute carrier family 7 member 11/ferroptosis

分类

医药卫生

引用本文复制引用

赵丽君,丁关鑫,黄菲,迪丽娜尔·亚尔麦麦提,吴顺华..亚砷酸钠致人肝星状细胞活化中铁死亡相关基因SLC7A11和CDKN1A的DNA甲基化及表达变化[J].环境与职业医学,2023,40(12):1403-1410,8.

基金项目

国家自然科学基金项目(82160650) (82160650)

环境与职业医学

OA北大核心CSCDCSTPCD

2095-9982

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