基础医学与临床 ›› 2011, Vol. 31 ›› Issue (1): 25-31.

• 研究论文 • 上一篇    下一篇

福辛普利和缬沙坦抑制AngⅡ诱导的大鼠肾小管上皮细胞klotho基因表达下调

林书典1,周巧玲2,詹锋1   

  1. 1. 海南省人民医院2. 中南大学 湘雅医学院 湘雅医院
  • 收稿日期:2009-11-23 修回日期:2010-06-10 出版日期:2011-01-05 发布日期:2011-01-05
  • 通讯作者: 林书典

Role of Fosinopril and Valsartan on Inhibiting Klotho Gene down-expression Induced by AngII

LIN Shu-dian 1,ZHOU Qiao-ling 2,Zhan Feng 2   

  1. 1. Hainan Province Hospital2.
  • Received:2009-11-23 Revised:2010-06-10 Online:2011-01-05 Published:2011-01-05
  • Contact: LIN Shu-dian

摘要: 目的 探讨福辛普利(Fos)和缬沙坦(Val)对血管紧张素Ⅱ(AngⅡ)抑制NRK-52E细胞klotho基因表达的干预作用及klotho与转化生长因子-β1(TGF-β1)的关系。方法 将大鼠肾小管上皮细胞(NRK-52E)分为对照组,AngⅡ(10-7mol/L)组,及AngⅡ分别再加Fos(10-5mol/L)组,Val(10-5mol/L)组, 和Fos+Val组,培养24h后,用反转录-多聚酶链反应(RT-PCR)检测klotho和TGF-β1 mRNA表达;用免疫组织化学法和Western Blot检测klotho和TGF-β1蛋白表达。对klotho和TGF-β1蛋白表达进行直线相关分析。结果 1.AngⅡ诱导NRK-52E中TGF-β1 mRNA表达上调,同时使klotho mRNA表达下调,经Fos或Val或Fos+Val干预后,TGF-β1 mRNA表达明显受抑制,而klotho mRNA显著上调表达(P<0.05)。2.Fos,Val和Fos+Val均明显上调AngⅡ诱导的klotho蛋白低表达(P<0.05),同时抑制TGF-β1蛋白高表达(P<0.05)。3. klotho和TGF-β1 蛋白表达呈直线负相关(r=-0.717,P<0.05)。结论 福辛普利和缬沙坦可上调AngⅡ诱导的klotho基因低表达,抑制TGF-β1高表达,klotho基因表达增强可能与TGF-β1表达下调有关。

Abstract: Objective To investigate role of Fosinopril (Fos) and Valsartan (Val) on klotho gene expression induced by Ang II and the relationship between klotho and TGF-β1. Motheds Culture cells, NRK-52E, were incubated with medias such as Ang II, Fos and Val. Five groups, control, AngII(10-7mol/L), AngII(10-7mol/L)+Fos(10-5mol/L), AngII(10-7mol/L)+Val(10-5mol/L) and AngII(10-7mol/L)+Fos(10-5mol/L)+Val (10-5mol/L) , were divided to observe the expression of the klotho and TGF-β1 mRNA and protein. The klotho and TGF-β1 mRNA were detected by reverse transcription – polymerase chain reaction (RT-PCR), immunohistochemistry (IHC) and Western Blotting (WB) was applied to determine the klotho and TGF-β1 protein expression. The linear relationship between klotho and TGF-β1 protein expression was analyzed by Pearson’s. Results 1. AngII induced an up-regulated expression of TGF-β1 mRNA , and associated with down-regulated klotho mRNA in NRK-52E as compared to control (all P<0.05); in cells incubated with Fos or Val or booth of all, the klotho mRNA expression was enheanced, and the TGF-β1 mRNA expression was diminished as compared to the AngII group(all P<0.05); combined Fos and Val could not enhance the expression of klotho gene, no significant different was showed as compared to the Fos group and Val group. 2. IHC and Western Blotting revealed that klotho protein was increased, TGF-β1 protein was decreased in Fos group, Val group and combination group as compared to AngII group, but no significantly different among the three groups was showed as compared to the Val group or Fos group. 3. Negative relationship was showed between klotho and TGF-β1 protein expression(r=-0.717, P<0.05). Conclusions Fosinopril and Valsartan can enhance the expression of klotho gene, and down-regulate TGF-β1 expression in NRK-52E, the increased level of klotho expression may be one of the important factor for preventing the renal fibrosis induced by TGF-β1.