香叶木素对RSL3诱导小鼠精母细胞GC-2铁死亡的抑制作用及其机制OA北大核心CSTPCD
Inhibitory effect of diosmetin on ferroptosis of GC-2 spermatocytes induced by RSL3 in mice and its mechanism
目的:探讨香叶木素(DIO)对谷胱甘肽过氧化物酶(GSH-Px)抑制剂(1S,3R)-RSL3(RSL3)诱导小鼠精母细胞GC-2铁死亡的抑制作用,并阐明相关作用机制.方法:GC-2细胞分为对照组、RSL3组、RSL3+0.8 nmol·L-1 DIO组、RSL3+4.0 nmol·L-1 DIO组、RSL3+20.0 nmol·L-1 DIO组和RSL3+铁死亡抑制剂Ferrostain-1(Fer-1)组(200 nmol·L-1 Fer-1).分别采用 0、1、5、10、50、100、500 和 1 000 nmol·L-1 RSL3 溶液及 0、0.1、0.5、1.0、5.0、10.0 和 50.0 μmol·L-1 DIO溶液处理细胞.另取GC-2细胞,分为空白组、模型组和给药组,给药组GC-2细胞按照处理方式分为 0.8、4.0和 20.0 nmol·L-1 DIO组及RSL3+0.8 nmol·L-1 DIO组、RSL3+4.0 nmol·L-1 DIO组和RSL3+20.0 nmol·L-1 DIO组.噻唑蓝(MTT)法检测各组GC-2细胞存活率.采用100 nmol·L-1 RSL3分别作用GC-2细胞0、6、12、24、36和48 h,Western blotting法检测各组GC-2细胞中铁死亡相关蛋白表达水平.试剂盒检测各组GC-2细胞中超氧化物歧化酶(SOD)活性和丙二醛(MDA)水平及谷胱甘肽(GSH)/氧化型谷胱甘肽(GSSG)比值,免疫荧光法观察各组GC-2细胞中酰基辅酶A合成酶长链家族成员4(ACSL4)蛋白荧光强度.结果:MTT法检测,与0 nmol·L-1 RSL3组比较,50、100、500 和 1 000 nmol·L-1 RSL3 组GC-2 细胞存活率均明显降低(P<0.01);与 0 μmol·L-1 DIO组比较,0.5、1.0、5.0、10.0和50.0 μmol·L-1 DIO组GC-2细胞存活率均明显降低(P<0.01),后续实验中选择100 nmol·L-1 RSL3作用GC-2细胞,DIO作用浓度<0.1 μmol·L-1.与空白组比较,模型组GC-2细胞存活率明显降低(P<0.01);与模型组比较,RSL3+20.0 nmol·L-1 DIO组细胞存活率明显升高(P<0.01).Western blotting法检测,与0 h比较,RSL3作用6 h时GC-2细胞中GPX4蛋白表达水平明显降低(P<0.01),RSL3作用12 h时GC-2细胞中HO-1蛋白表达水平明显升高(P<0.05),GPX4和FTH1蛋白表达水平均明显降低(P<0.05或P<0.01),RSL3作用24 h时GC-2细胞中GPX4和HO-1蛋白表达水平明显降低(P<0.05或P<0.01),RSL3作用36和48 h时GC-2细胞中HO-1蛋白表达水平均明显降低(P<0.01);将100 nmol·L-1 RSL3作用GC-2细胞12 h作为后续实验条件.与对照组比较,RSL3组GC-2细胞中MDA水平明显升高(P<0.01),SOD活性和GSH/GSSG比值均明显降低(P<0.05);与RSL3组比较,RSL3+0.8 nmol·L-1 DIO组、RSL3+4.0 nmol·L-1 DIO组、RSL3+20.0 nmol·L-1 DIO组和RSL3+Fer-1 组GC-2 细胞中SOD活性均明显升高(P<0.05或P<0.01),RSL3+20.0 nmol·L-1 DIO组和RSL3+Fer-1组GC-2细胞中MDA水平均明显降低(P<0.05或P<0.01),RSL3+4.0 nmol·L-1 DIO组、RSL3+20.0 nmol·L-1 DIO组和RSL3+Fer-1组GC-2细胞中GSH/GSSG比值均明显升高(P<0.05或P<0.01).免疫荧光法观察,与对照组比较,RSL3组GC-2细胞中ACSL4蛋白荧光强度明显增强;与RSL3组比较,RSL3+0.8 nmol·L-1 DIO组、RSL3+4.0 nmol·L-1 DIO组、RSL3+20.0 nmol·L-1 DIO组和RSL3+Fer-1组GC-2细胞中ACSL4蛋白荧光强度均明显减弱.Western blotting法检测,与对照组比较,RSL3组GC-2细胞中HO-1蛋白表达水平升高(P<0.05),GPX4和FTH1蛋白表达水平均明显降低(P<0.05或P<0.01);与RSL3组比较,RSL3+0.8 nmol·L-1 DIO组、RSL3+4.0 nmol·L-1 DIO组、RSL3+20.0 nmol·L-1 DIO组和RSL3+Fer-1组GC-2细胞中HO-1蛋白表达水平均明显降低(P<0.05或P<0.01),GPX4和FTH1蛋白表达水平均明显升高(P<0.05或P<0.01).结论:DOI能够减轻RSL3诱导的小鼠精母细胞GC-2铁死亡,其机制可能与抑制HO-1蛋白表达,上调GPX4和FTH1蛋白表达有关.
Objective:To discuss the inhibitory effect of diosmetin(DIO)on the ferroptosis induced by the glutathione peroxidase(GSH-Px)inhibitor(1S,3R)-RSL3(RSL3)in spermatocytes GC-2 of the mice,and to clarify the mechanism.Methods:The GC-2 cells were divided into control group,RSL3 group,RSL3+0.8 nmol·L-1 DIO group,RSL3+4.0 nmol·L-1 DIO group,RSL3+20.0 nmol·L-1 DIO group,and RSL3+ferroptosis inhibitor Ferrostain-1(Fer-1)group(200 nmol·L-1 Fer-1).The cells were treated with 0,1,5,10,50,100,500,and 1 000 nmol·L-1 RSL3 solutions,and 0,0.5,0.1,1.0,5.0,10.0,and 50.0 μmol·L-1 DIO solutions,respectively.Additionally,the GC-2 cells were divided into blank group,model group,and treatment group.The GC-2 cells in treatment group were further divided into 0.8,4.0,and 20.0 nmol·L-1 DIO groups,as well as RSL3+0.8 nmol·L-1 DIO group,RSL3+4.0 nmol·L-1 DIO group,and RSL3+20.0 nmol·L-1 DIO group.MTT method was used to detect the survival rates of the GC-2 cells in various groups.The GC-2 cells were treated with 100 nmol·L-1 RSL3 for 0,6,12,24,36,and 48 h;Western blotting method was used to detect the expression levels of ferroptosis-related proteins in the GC-2 cells in various groups;kits were used to detect the activities of superoxide dismutase(SOD),levels of malondialdehyde(MDA),and ratios of glutathione(GSH)to glutathione disulfide(GSSG)in the GC-2 cells in various groups;immunofluorescence method was used to detect the fluorescence intensities of acyl-CoA synthetase long-chain family member 4(ACSL4)protein in the GC-2 cells in various groups.Results:The MTT method results showed that compared with 0 nmol·L-1 RSL3 group,the survival rates of the GC-2 cells in 50,100,500,and 1 000 nmol·L-1 RSL3 groups were significantly decreased(P<0.01);compared with 0 μmol·L-1 DIO group,the survival rates of the GC-2 cells in 0.5,1.0,5.0,10.0,and 50.0 μmol·L-1 DIO groups were significantly decreased(P<0.01),and 100 nmol·L-1 RSL3 with DIO concentration<0.1 μmol·L-1 were selected for the subsequent experiments.Compared with blank group,the survival rates of the GC-2 cells in model group was significantly decreased(P<0.01);compared with model group,the survival rates of the GC-2 cells in RSL3+20.0 nmol·L-1 DIO group was significantly increased(P<0.01).The Western blotting results showed that compared with 0 h,the expression level of GPX4 protein in the GC-2 cells was significantly decreased after treated with RSL3 for 6 h(P<0.01),and the expression level of HO-1 protein was significantly increased after treated with RSL3 for 12 h(P<0.05);after treated with RSL3 for 12 h,the expression levels of GPX4 and FTH1 proteins were significantly decreased(P<0.05 or P<0.01);after treated with RSL3 for 24 h,the expression levels of GPX4 and HO-1 proteins were significantly decreased(P<0.05 or P<0.01);after treated with RSL3 for 36 and 48 h,the expression levels of HO-1 protein were significantly decreased(P<0.01).Therefore,100 nmol·L-1 RSL3 and for 12 h were selected as the experimental condition for the subsequent experiments.Compared with control group,the MDA level in the GC-2 cells in RSL3 group was significantly increased(P<0.01),and the SOD activity and GSH/GSSG ratio were significantly decreased(P<0.05).Compared with RSL3 group,the SOD activities in the cells in RSL3+0.8 nmol·L-1 DIO group,RSL3+4.0 nmol·L-1 DIO group,RSL3+20.0 nmol·L-1 DIO group,and RSL3+Fer-1 group were significantly increased(P<0.05 or P<0.01).The MDA levels in the cells in RSL3+20.0 nmol·L-1 DIO group and RSL3+Fer-1 group were significantly decreased(P<0.05 or P<0.01),and the GSH/GSSG ratio in the cells in RSL3+4.0 nmol·L-1 DIO group,RSL3+20.0 nmol·L-1 DIO group,and RSL3+Fer-1 group were significantly increased(P<0.05 or P<0.01).The immunofluorescence observation results showed that compared with control group,the fluorescence intensity of ACSL4 protein in the GC-2 cells in RSL3 group was significantly increased;compared with RSL3 group,the fluorescence intensities of ACSL4 protein in the cells in RSL3+0.8 nmol·L-1 DIO group,RSL3+4.0 nmol·L-1 DIO group,RSL3+20.0 nmol·L-1 DIO group,and RSL3+Fer-1 group were significantly decreased.The Western blotting results showed that compared with control group,the expression level of HO-1 protein in the cells in RSL3 group was increased(P<0.05),and the expression levels of GPX4 and FTH1 proteins were significantly decreased(P<0.05 or P<0.01);compared with RSL3 group,the expression levels of HO-1 protein in the cells in RSL3+0.8 nmol·L-1 DIO group,RSL3+4.0 nmol·L-1 DIO group,RSL3+20.0 nmol·L-1 DIO group,and RSL3+Fer-1 group were significantly decreased(P<0.05 or P<0.01),and the expression levels of GPX4 and FTH1 proteins were significantly increased(P<0.05 or P<0.01).Conclusion:DIO can alleviate the RSL3-induced ferroptosis in the GC-2 spermatocytes of the mice,and its mechanism may be related to the inhibition of HO-1 protein expression and the upregulation of expressions of GPX4 and FTH1 proteins.
马宝莲;胡晓雪;艾霄文;张永兰
重庆理工大学药学与生物工程学院药理学教研室,重庆 400054重庆理工大学药学与生物工程学院药理学教研室,重庆 400054重庆理工大学药学与生物工程学院药理学教研室,重庆 400054重庆理工大学药学与生物工程学院药理学教研室,重庆 400054
药学
铁死亡香叶木素小鼠精母细胞GC-2谷胱甘肽过氧化酶4铁蛋白重链1酰基辅酶A合成酶长链家族成员4
FerroptosisDiosmetinMouse spermatocyte GC-2Glutathione peroxidase 4Ferritin heavy chain 1Acyl-CoA synthetase long-chain family member 4
《吉林大学学报(医学版)》 2024 (6)
1481-1490,10
国家自然科学基金青年基金项目(81803800)重庆市科技局自然科学基金项目(CSTC2018jcyjAX0529,CSTB2023NSCQ-MSX0469)
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