首页|微小RNA-138/NGAL对缺血再灌注诱导人肾小管上皮细胞的影响

微小RNA-138/NGAL对缺血再灌注诱导人肾小管上皮细胞的影响

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目的 探究微小 RNA-138(microRNA-138,miR-138)调控中性粒细胞明胶酶相关脂质运载蛋白(neutrophil gelatinase-associated lipocalin,NGAL)对缺血/再灌注(ischemia/reperfusion,I/R)诱导人肾小管上皮(HK-2)细胞损伤的影响.方法 HK-2 细胞构建I/R模型,分别转染miR-138 模拟物、miR-138 抑制剂、NGAL、NGAL + miR-138 模拟质粒,qRT-PCR测定不同细胞miR-138 或NGAL mRNA表达鉴定转染结果,细胞活力检测(cell counting kit-8,CCK-8)法和流式细胞术测定细胞活性和凋亡.ELISA、Western blot法分别测定miR-138 模拟物、miR-138 抑制剂对I/R细胞白细胞介素(interleukin,IL)-6、IL-1β、肿瘤坏死因子-α(tumor necrosis factor-α,TNF-α)水平,以及Toll样受体 4(toll like receptor 4,TLR4)、核因子κB(nuclear factor kappa-B,NF-κB)、NF-κB抑制蛋白(inhibitor-NF-κB,IκBα)、磷酸IκBα(p-IκBα)、NGAL蛋白表达的影响.结果 I/R细胞miR-138 mRNA表达、细胞活力降低,凋亡增加(P<0.01).质粒转染成功,miR-138 模拟物促进IR细胞活力,降低凋亡和NGAL mRNA表达(P<0.01);miR-138 抑制剂、NGAL 模拟降低IR细胞活力,增加凋亡和NGAL mRNA表达(P<0.01);NGAL 模拟对IR细胞的损伤作用可被miR-138 模拟逆转.miR-138 抑制剂可增加I/R细胞IL-6、IL-1β、TNF-α水平和凋亡,上调TLR4、NF-κB、p-IκBα、NGAL蛋白表达,下调IκBα蛋白表达(P<0.05);miR-138 模拟物可降低I/R细胞IL-6、IL-1β、TNF-α水平和凋亡,下调TLR4、NF-κB、p-IκBα、NGAL蛋白表达,上调IκBα蛋白表达(P<0.05).结论 miR-138 通过调节NGAL和TLR4/NF-κB途径降低细胞凋亡和炎症因子水平,对I/R诱导的HK-2 细胞发挥保护作用.
Effect of microRNA-138 on the ischemia/reperfusion of human renal tubular epithelial cells
Objective To explore the effect of microRNA-138(miR-138)on injury of ischemia/reperfusion(I/R)induced human renal tubular epithelium(HK-2)cells through neutrophil gelatinase-associated lipocalin(NGAL).Methods HK-2 cells were used to construct I/R model cells,and transfected with miR-138 mimic,miR-138 inhibitor,NGAL,NGAL + miR-138 mimic plasmids,respectively.qRT-PCR determined the expression of miR-138 or NGAL mRNA in different cells to identify the transfection results.Cell counting kit-8(CCK-8)method and flow cytometry were used to detected the activities and apoptosis of cells.ELISA and western blot were used to determine the effects of miR-138 mimic or miR-138 inhibitor on levels of interleukin(IL)-6,IL-1β,tumor necrosis factor(TNF-α)and protein expression of toll like receptor 4(TLR4),nuclear factor kappa-B(NF-κB),inhibitor of NF-κB(IκBα),pho-IκBα(p-IκBα),NGAL of cells.Results miR-138 mRNA expression and cell activity were decreased,while apoptosis increased in I/R cells(P<0.01).Plasmid transfected well,miR-138 mimic increased activity while decreased apoptosis and NGAL mRNA expression of I/R cell.miR-138 inhibitor or NGAL mimic inhibited activity and increased apoptosis and NGAL mRNA expression of I/R cell.The negative effects of NGAL mimic on I/R cell were reversed by miR-138 mimic.miR-138 inhibitor increased levels of IL-6,IL-1β,TNF-α of I/R cell,and increased TLR4,NF-κB,p-IκBα,NGAL protein expression and decreased IκBα protein expression(P<0.05).While miR-138 mimic decreased levels of IL-6,IL-1β,TNF-α of I/R cell,and decreased TLR4,NF-κB,p-IκBα,NGAL protein expression and increased IκBα protein expression(P<0.05).Conclusion miR-138 reduced apoptosis and inflammation factor levels to play a protective role on I/R induced HK-2 cells may through regulating NGAL and TLR4/NF-κB pathway.

Human renal tubular epithelial cellsIschemia/reperfusionNeutrophil gelatinase related lipid transporterTLR4/NF-κ B pathway

邱冬豪

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浙江大学附属杭州市第一人民医院肾内科,浙江杭州 310008

人肾小管上皮细胞 缺血/再灌注 中性粒细胞明胶酶相关脂质运载蛋白 TLR4/NF-κB通路

浙江省杭州市科技计划引导项目

20201231Y024

2024

中国现代医生
中国医学科学院

中国现代医生

影响因子:1.571
ISSN:1673-9701
年,卷(期):2024.62(11)
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