设为首页 电子邮箱 联系我们

本刊最新招聘信息请见“通知公告”!  本刊投稿系统试运行中,欢迎投稿!如投稿有问题,可直接将稿件发送至zgyy8888@163.com

 

主管单位:中华人民共和国   

国家卫生健康委员会

主办单位:中国医师协会
总编辑:
杨秋

编辑部主任:吴翔宇

邮发代号:80-528
定价:28.00元
全年:336.00元
Email:zgyy8888@163.com
电话(传真):010-64428528;
010-64456116(总编室)

                  

过刊目录

2022 年第 8 期 第 17 卷

阿司匹林对碘海醇诱导的肾损伤肾小管上皮细胞线粒体的保护作用及相关机制研究

Protective effect of aspirin on mitochondrion in renal tubular epithelial cells damaged by iohexol and its related mechanisms

作者:苟晓燕吕梁撒亚莲曾泽群

英文作者:Gou Xiaoyan Lyu Liang Sa Yalian Zeng Zequn

单位:昆明理工大学附属医院放射科,昆明650034

英文单位:Department of Radiology Affiliated Hospital of Kunming University of Science and Technology Kunming 650034 China

关键词:阿司匹林;碘海醇;人肾小管上皮细胞;线粒体

英文关键词:Aspirin;Iohexol;Humanrenaltubularepithelialcells;Mitochondrion

  • 摘要:
  • 目的 探索阿司匹林对碘海醇诱导的肾损伤肾小管上皮细胞线粒体的保护作用及相关机制。方法 将人肾小管上皮细胞(HK-2)分为正常对照组(Control组,HK-2细胞不特殊处理),碘海醇处理组(Iohexol组,HK-2细胞+18.86 mgI/ml的碘海醇),阿司匹林组处理组(aspirin组,HK-2细胞+2.5 μmol/L的阿司匹林),碘海醇+阿司匹林处理组(Iohexol2组,HK-2细胞+18.86 mgI/ml的碘海醇+2.5 μmol/L的阿司匹林)。电镜观察各组细胞线粒体融合、分裂情况;流式细胞术检测细胞凋亡;免疫荧光检测线粒体活性氧自由基(ROS)的表达;收集HK-2细胞进行真核有参转录组测序分析;蛋白印迹法验证通路相关蛋白表达。结果 Control组比较,Iohexol组和aspirin组中线粒体分裂增多、融合减少;与Iohexol组比较,Iohexol2组及aspirin组线粒体分裂减少、融合增多。Iohexol2HK-2细胞凋亡率低于Iohexol组和aspirin组[(26.5±1.3%比(71.8±4.3%、(32.3±5.0%(P0.001P=0.041)Iohexol2组中ROS生成少于Iohexol(P=0.002)。真核有参转录组测序分析结果显示,Iohexol组与Iohexol2组细胞丝裂原活化蛋白激酶通路具有明显差异。Iohexol2组细胞外调节蛋白激酶1/2ERK1/2)与磷酸化ERK1/2比值、c-MYC结合蛋白及线粒体分裂动力相关蛋白1(DRP1)等蛋白表达水平均低于Iohexol组及aspirin组(均P0.01)。结论 阿司匹林可通过介导ERK1/2/c-MYC/DRP1信号通路减少碘海醇诱导的HK-2细胞线粒体的分裂。

  • Objective To explore the protective effect of aspirin on mitochondrion in renal tubular epithelial cells damaged by iohexol and its related mechanisms. Methods Human renal tubular epithelial cells (HK-2) were divided into normal control group (control group, HK-2 cells without special treatment), iohexol treatment group (Iohexol group, HK-2 cells + 18.86 mgI/ml iohexol), aspirin treatment group (aspirin group, HK-2 cells+2.5 μmol/L aspirin), iohexol+aspirin treatment group (Iohexol2 group, HK-2 cells+18.86 mgI/ml iohexol+2.5 μmol/L aspirin). Mitochondrial fusion and division after experimental treatment were observed by transmission electron microscope. Cell apoptosis was detected by flow cytometry. Mitochondrial reactive oxygen species (ROS) in HK-2 cells was detected by immunofluorescence. HK-2 cells were collected for transcriptome gene sequencing analysis. The expression of pathway-related proteins was verified by western blotting. Results Compared with control group, mitochondrial division increased and fusion decreased in Iohexol group and aspirin group. Compared with Iohexol group, mitochondrial division decreased and fusion increased in Iohexol2 group and aspirin group. The apoptosis rate of HK-2 cells in Iohexol2 group was lower than that in Iohexol group and aspirin group (26.5±1.3)% vs (71.8±4.3)%, (32.3±5.0)%(P0.001, P=0.041). The production of ROS in Iohexol2 group was less than that in Iohexol group(P=0.002). Transcriptome gene sequencing analysis showed that there were significant differences in mitogen activated protein kinase pathway between Iohexol group and Iohexol2 group. The expression levels of extracellular regulated protein kinase 1/2 (ERK1/2) to phosphorylated ERK1/2 ratio, c-MYC binding protein and mitochondrial division dynamics related protein 1 (DRP1) in Iohexol2 group were significantly lower than those in Iohexol group and aspirin group (all P0.01). Conclusion Aspirin can reduce mitochondrial division induced by iohexol in HK-2 cells by mediating ERK1/2/c-MYc/DRP1 signaling pathway.

copyright 《中国医药》杂志编辑部
地址:北京市朝阳区安贞路2号首都医科大学附属北京安贞医院北楼二层
电话:010-64456116 传真:010-64428528 邮编:100029 Email: zgyy8888@163.com
网址:www.chinamedicinej.com 京ICP备2020043099号-3

当您在使用本网站投稿遇到困难时,请直接将稿件投送到编辑部邮箱zgyy8888@163.com。







安卓


苹果

关闭