基础医学与临床 ›› 2015, Vol. 35 ›› Issue (2): 152-156.

• 研究论文 • 上一篇    下一篇

高浓度尿素诱导人脑微血管内皮细胞产生炎性因子

王琦1,王弘凯1,刘丽君1,何菲2,汪克建3,李晋芳2,冉建华1   

  1. 1. 重庆医科大学基础医学院
    2. 重庆医科大学
    3. 重庆医科大学基础医学院电镜教研室
  • 收稿日期:2014-09-01 修回日期:2014-10-22 出版日期:2015-02-05 发布日期:2015-01-23
  • 通讯作者: 冉建华 E-mail:1315038024@qq.com
  • 基金资助:
    国家自然科学基金;重庆市教委项目;重庆市卫生局项目;重庆市渝中区科委项目

High concentrations of urea induces human brain microvascular endothelial cells to produce inflammatory cytokines

  • Received:2014-09-01 Revised:2014-10-22 Online:2015-02-05 Published:2015-01-23

摘要: 目的 研究高浓度尿素诱导人脑微血管内皮细胞(HBMECs)产生炎性因子及其机制。方法 以相同渗透压的甘露醇为对照,高浓度尿素(25 mmol/L)干预 HBMECs 3、6、12和24 h后,免疫荧光法观察细胞内肿瘤坏死因子 ?(TNF-?)和诱导型一氧化氮合酶(iNOS)的表达。蛋白免疫印迹法(Western blot)检测TNF-?、iNOS、环氧合酶-2(cycloxygenase-2,COX-2)、核因子κB(NF-κB) /P65和p-P65的表达水平。NO 试剂盒检测细胞 NO 含量。结果 高浓度尿素增强细胞内 TNF-? 和 iNOS 表达。细胞 TNF-?、COX-2 和 p-P65 蛋白水平在3和6 h明显高于对照组(P<0.01);iNOS 蛋白水平持续增高(P<0.01)。NO含量在3 h明显增多(P<0.05)。结论 高浓度尿素诱导人脑微血管内皮细胞产生炎性因子。

关键词: 尿素, 人脑微血管内皮细胞, TNF-a, NO, NF-κB

Abstract: Objective To explore high concentrations of urea-induced human brain microvascular endothelial cells (HBMECs) to produce inflammatory cytokines and possible mechanism. Methods HBMECs were incubated in high concentrations of urea or mannitol(as osmotic control) for 3,6,12 and 24 hours. Expressions of TNF-a and iNOS were observed by Immunofluorescence. Western blot analysis was employed to assess the protein expressions of TNF-a, iNOS, COX-2, NF-κB/P65 and p-P65. NO concentration was determined by a commercial NO assay kit. Results Immunofluorescence showed high positive immunostaining of TNF-a and iNOS after high concentrations of urea stimulued compared with control group .The protein expressions of TNF-a, COX-2 and p-P65 were significantly increased at 3 and 6 hours after high urea treatment (p<0.01), and iNOS were continued to increase from 3 to 24 hours (p<0.01).Moreover, NO content was increased at 3 hours after high urea treatment (p<0.05). Conclusion High concentrations of urea can induce HBMECs to produce inflammatory cytokines.

Key words: urea, HBMECs, TNF-a, NO, NF-κB

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