首页|依达拉奉经MAPKs通路对脂多糖激活的小胶质细胞Sirt3表达调控

依达拉奉经MAPKs通路对脂多糖激活的小胶质细胞Sirt3表达调控

扫码查看
目的 探究依达拉奉对LPS激活的小胶质细胞Sirt3和MAPKs通路相关蛋白的作用及其调控机制.方法 采用Western blot和免疫荧光双标染色检测LPS激活的BV2小胶质细胞中Sirt3和MAPKs通路相关蛋白ERK1/2、P38、JNK及p-ERK1/2、p-P38和p-JNK的表达;检测ERK1/2通路抑制剂处理后p-ERK1/2和Sirt3的表达.结果 LPS激活的BV细胞中Sirt3、p-ERK1/2、p-P38和p-JNK表达显著增高,依达拉奉能促进Sirt3和p-ERK1/2过表达,并降低p-P38和p-JNK表达;ERK1/2抑制后p-ERK1/2和Sirt3的蛋白表达降低.依达拉奉可促进激活的BV2细胞中Sirt3和p-ERK1/2过表达,并下调过表达的p-P38和p-JNK.结论 依达拉奉可调节BV2细胞中MAPKs信号通路并促进Sirt3生成,可能经ERK/Sirt3通路发挥抗炎作用.
Edaravone regulates Sirt3 expression in lipopolysaccharide-activated microglia via MAPKs signaling pathway
Objective To investigate the effect of edaravone on Sirt3 and MAPKs pathway-related proteins in LPS-activated microglia and its regulatory mechanism.Methods Western Blot and immunofluorescence were used to detect the effect of edaravone on the protein expression of Sirt3 and MAPKs pathway-related proteins ERK1/2,P38,JNK as well as their phosphorylated forms p-ERK1/2,p-P38 and p-JNK in the activated BV2 cells.Western Blot techniques were applied to detect the effects of ERK1/2 pathway inhibitor on the expressions of p-ERK1/2 and Sirt3.Results The expressions of Sirt3,p-ERK1/2,p-P38 and p-JNK in microglia were significantly increased after BV2 cells activation.Edaravone promoted the expression of Sirt3 and p-ERK1/2 and downregulated the expression of p-JNK and p-P38.The protein expression of Sirt3 and p-ERK1/2 decreased after co-treatment with edaravone and ERK1/2 inhibitor.Edaravone promoted the overexpression of Sirt3 and p-ERK1/2 and downregulated the expression of p-JNK and p-P38.Conclusions Edaravone can regulate MAPKs signaling pathway and promote Sirt3 production in BV2 cells,possibly regulates neuroinflammatory responses via ERK/Sirt3 signaling pathway.

EdaravoneSirt3MicrogliaMAPKs signaling pathway

祁志、杨力、贾秋叶、陈浩伦、段兆达、吴春云

展开 >

昆明医科大学基础医学院人体解剖与组织胚胎学系,昆明 650500

依达拉奉 Sirt3 小胶质细胞 MAPKs信号通路

国家自然科学基金云南省科技厅昆明医科大学联合专项云南省大学生创新性实验计划项目昆明医科大学大学生创新性实验计划项目

81960223202301AY070001-1632022JXD301

2024

中国临床解剖学杂志
中国解剖学会

中国临床解剖学杂志

CSTPCD北大核心
影响因子:0.7
ISSN:1001-165X
年,卷(期):2024.42(1)
  • 14