Your browser doesn't support javascript.
loading
The Effect of Ferroptosis on the Activation of Human Hepatic Stellate Cells Induced by Inorganic Arsenic / 医学研究杂志
Journal of Medical Research ; (12): 45-49, 2024.
Article in Zh | WPRIM | ID: wpr-1023596
Responsible library: WPRO
ABSTRACT
Objective To investigate the effect of NaAsO2 on ferroptosis in human hepatic stellate cells(LX-2).Methods LX-2 cells were cultured in vitro,and different concentrations of NaAsO2(5μmol/L,10μmol/L,15μmol/L)were infected with LX-2 cells for 24h in a group design to construct the activation model of LX-2 induced by NaAsO2 in vitro,and a control group was set up.Mitochon-drial structure of LX-2 cells treated with NaAsO2 was observed by transmission electron microscopy(TEM).Fe2+levels were detected by fluorescence microscope and fluorescent enzyme label.The content of malondialdehyde(MDA)was determined by the colorimetric meth-od.The protein expression levels of SLC7A11,GPX4,and α-smooth muscle actin(α-SMA)were detected by Western blot.Results TEM showed that mitochondrial membrane integrity was damaged and mitochondrial ridges were reduced and disappeared in the NaAsO2group.In addition,compared with the control group,Fe2+levels in NaAsO2 treatment groups were increased(P<0.05).There were statistically significant differences in MDA content among different doses of NaAsO2groups(F=7.18,P<0.05).Compared with the control group,MDA content of LX-2 cells in 5 and 15μmol/L NaAsO2groups was higher than that in the control group(P<0.05).At the translation level,the expression of fibrosis index α-SMA protein level was up-regulated with the increase of NaAsO2dose(P<0.05),the protein expression levels of ferroptosis index SLC7A11 and GPX4decreased in a dose-dependent manner with the increase of the dose of NaAsO2(P<0.05).Conclusion Ferroptosis is involved in the activation of LX-2 cells induced by NaAsO2.
Key words
Full text: 1 Database: WPRIM Language: Zh Journal: Journal of Medical Research Year: 2024 Document type: Article
Full text: 1 Database: WPRIM Language: Zh Journal: Journal of Medical Research Year: 2024 Document type: Article