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辛伐他汀对香烟烟雾提取物诱导的人脐静脉内皮细胞表达sEPCR和mEPCR的影响
引用本文:樊芳芳,胡晓芸,扈丽娟,韩葆芬,赵瑛娟.辛伐他汀对香烟烟雾提取物诱导的人脐静脉内皮细胞表达sEPCR和mEPCR的影响[J].中国病理生理杂志,2012,28(4):727-729.
作者姓名:樊芳芳  胡晓芸  扈丽娟  韩葆芬  赵瑛娟
作者单位:山西医科大学第一医院呼吸内科, 山西 太原 030001
基金项目:山西省卫生厅科技攻关计划项目
摘    要:目的: 研究辛伐他汀对香烟烟雾提取物(CSE)诱导的人脐静脉内皮细胞(HUVECs) 表达可溶性内皮细胞蛋白C受体(sEPCR)和膜联内皮细胞蛋白C受体(mEPCR)的干预作用。方法: 体外培养的4~6代HUVECs 随机分为对照组、5%CSE组、不同浓度辛伐他汀组及辛伐他汀干预组,辛伐他汀组分别加入50、100、200 μmol/L辛伐他汀液孵育24 h,辛伐他汀干预组先以50、100、200 μmol/L辛伐他汀预处理细胞2 h,再与5%CSE孵育24 h。收集各组细胞及上清液,ELISA法检测上清液中sEPCR蛋白含量,实时定量PCR法检测各组细胞中mEPCR mRNA的表达。结果: (1)5%CSE组sEPCR蛋白含量高于对照组,mEPCR mRNA表达低于对照组,差异均有统计学意义(均P<0.05);(2)100 μmol/L与200 μmol/L辛伐他汀组sEPCR蛋白含量均高于对照组,低于5%CSE组,其mEPCR mRNA表达均低于对照组,高于5%CSE组,差异均有统计学意义(均P<0.05);(3)各辛伐他汀干预组sEPCR蛋白含量均低于5%CSE组,但高于对照组及相应浓度的辛伐他汀组;相反,各辛伐他汀干预组mEPCR mRNA表达均高于5%CSE组,低于对照组及相应浓度的辛伐他汀组,差异均有统计学意义(均P<0.05)。结论: 在体外,辛伐他汀通过上调HUVECs mEPCR mRNA的表达,降低sEPCR的分泌,对CSE介导的内皮细胞凝血功能障碍可能具有一定的改善作用。

关 键 词:香烟烟雾提取物  内皮细胞蛋白C受体  人脐静脉内皮细胞  
收稿时间:2011-10-17

Effects of simvastatin on cigarette smoke extract-induced sEPCR and EPCR expression in human umbilical vein endothelial cells
FAN Fang-fang , HU Xiao-yun , HU Li-juan , HAN Bao-fen , ZHAO Ying-juan.Effects of simvastatin on cigarette smoke extract-induced sEPCR and EPCR expression in human umbilical vein endothelial cells[J].Chinese Journal of Pathophysiology,2012,28(4):727-729.
Authors:FAN Fang-fang  HU Xiao-yun  HU Li-juan  HAN Bao-fen  ZHAO Ying-juan
Institution:Department of Respiratory Medicine, The First Affiliated Hospital, Shanxi Medicine University, Taiyuan 030001, China
Abstract:AIM: To investigate the effects of simvastatin on cigarette smoke extract(CSE)-induced expression levels of soluble endothelial cell protein C receptor(sEPCR) and membrane-associated endothelial cell protein C receptor(mEPCR) in human umbilical vein endothelial cells(HUVECs).METHODS: Cultured HUVECs at passage 4 to 6 were randomly divided into control group,5% CSE group,simvastatin groups and simvastatin+CSE groups.In simvastatin groups,HUVECs were incubated with simvastatin at the concentrations of 50,100 and 200 μmol/L for 24 h.In simvastatin+CSE groups,the cells were treated with simvastatin at the concentrations of 50,100 and 200 μmol/L for 2 h,and then exposed to CSE for 24 h.The protein level of sEPCR in the culture supernatants was measured by ELISA.The cells were collected for determining the mRNA expression of mEPCR by real-time PCR.RESULTS: Compared with control group,the protein level of sEPCR was significantly increased,and the mRNA expression of mEPCR was significantly decreased in 5% CSE group(both P<0.05).The protein levels of sEPCR were significantly increased,and the mRNA expression of mEPCR was significantly decreased in 100 μmol/L and 200 μmol/L simvastatin groups.However,the protein levels of sEPCR were lower,and the mRNA expression of mEPCR was significantly higher in 100 μmol/L and 200 μmol/L simvastatin groups than those in 5% CSE group.Compared with 5% CSE group,the protein levels of sEPCR in simvastatin+CSE groups were significantly decreased,but higher than those in control group and simvastatin group with corresponding concentration.On the contrary,the mRNA expression of mEPCR in simvastatin+CSE groups was significantly increased,but lower than that in control group and simvastatin group with corresponding concentration(all P<0.05).CONCLUSION: Simvastatin obviously increases the mRNA expression of mEPCR,decreases the protein level of sEPCR,and attenuates the CSE-induced endothelial injury in vitro.
Keywords:Cigarette smoke extract  Endothelial cell protein C receptor  Human umbilical vein endothelial cells
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