吉林大学学报(医学版) ›› 2013, Vol. 39 ›› Issue (3): 565-569.doi: 10.7694/jldxyxb20130329

• 基础研究 • 上一篇    下一篇

配对盒基因2对正常肾小管上皮细胞间充质转分化的诱导作用

李里1,2,南晓娟1,吴玉斌1   

  1. 1.中国医科大学附属盛京医院小儿肾脏风湿免疫科,辽宁 沈阳110004;2.辽宁医学院附属第一医院儿科,辽宁 锦州121000
  • 收稿日期:2012-09-24 出版日期:2013-05-28 发布日期:2013-07-01
  • 通讯作者: 吴玉斌(Tel:024- 83955555,E-mail:wuyb@sj-hospital.org) E-mail:wuyb@sj-hospital.org
  • 作者简介:李 里(1978-),女,辽宁省锦州市人,在读医学博士,主要从事小儿肾脏疾病的研究。
  • 基金资助:

    辽宁省沈阳市科学技术计划项目资助课题(F10-205-1-29);盛京医院博士优秀课题基金资助课题(ma26)

Induction of PAX2 on epithelial-mesenchymal transition in normal renal tubular epithelial cells

LI Li1,2,NAN Xiao-juan1,WU Yu-bin1   

  1. 1.Department of Pediatric Nephrology and  Rheumatism Immmunity,Shengjing Hospital,China Medical University,Shenyang 110004,China;2.Department of Pediatrics, First Affiliated Hospital,Liaoning Medical College,Jinzhou 121000,China
  • Received:2012-09-24 Online:2013-05-28 Published:2013-07-01

摘要: [摘 要] 目的:观察体外转染配对盒基因2(PAX2)对肾小管上皮细胞表型标志物的影响,探讨PAX2诱导转分化的作用,为肾纤维化治疗提供依据。方法:正常肾小管上皮细胞株NRK52E分为对照组、空载组(转染pGC-Fu空质粒)和转染组(采用脂质体转染法将pGC-FU-GFP-PAX2质粒转染至细胞中)。转染72 h后应用倒置相差显微镜观察各组细胞形态,应用Western blotting法和Real-time PCR法检测PAX2蛋白和mRNA表达水平;转染72 h后应用免疫组织化学法、Western blotting法和Real-time PCR法检测各组细胞E-钙黏蛋白(E-cadherin) 和α-肌动蛋白(α-SMA)及其mRNA表达水平。结果:pGC-FU-GFP-PAX2转染72 h后,转染组细胞绿色荧光强度较对照组明显增强,且肾小管上皮细胞的形态伸长; Western blotting法检测,转染组PAX2蛋白表达水平明显高于空载组和对照组(P<0.05);Real-time PCR检测,转染组细胞的PAX2mRNA表达水平明显高于空载组和对照组(P<0.05);转染组细胞中的E-cadherin染色较空载组和对照组明显减弱;α-SMA染色较空载组和对照组明显增强。Western blotting法检测,转染组细胞中E-cadherin表达水平明显低于空载组和对照组(P<0.05);α-SMA表达水平明显高于空载组和对照组(P<0.05);Real-time PCR检测,转染组细胞中E-cadherin mRNA表达水平明显低于空载组和对照组(P<0.05);α-SMA mRNA表达水平明显高于空载组和对照组(P<0.05)。结论:PAX2转染正常肾小管上皮细胞后E-cadherin表达减少,α-SMA表达增加,PAX2可能在体外诱导正常肾小管上皮细胞间充质转分化。

关键词:  , 配对盒基因2, 肾小管上皮细胞, 转分化, 转染

Abstract: Abstract:Objective To observe the effect of paired box gene 2 (PAX2) on the surface markers of renal tubular epithelial cells and induction of PAX2 on epithelial-mesenchymal transition (EMT) in vitro,and to provide basis for treatment of renal fibrosis. Methods The  rat normal renal tubular epithelial cell line NRK52E were divided into  control group,empty vector group(transfected with pGC-FU empty vector),and transfection group(transfected  with pGC-FU-GFP-PAX2 vector). The morphology of cells 72 h after transfection was evaluated by inverted phase contrast microscope. The expression levels of PAX2 protein and mRNA were evaluated by Western blotting and Real-time PCR methods.72 h after transfection,the expressions of E-cadherin and α-smooth muscle actin (α-SMA)  and their mRNA expressions were detected by  immunohistochemistry,Western blotting and Real-time PCR methods. Results 72 h after  tranfection of pGC-FU-GFP-PAX2,the fluorescence intensity   in transfection group was stronger than that in control group,and the shape of renal tubular epithelial cells  elongated.The  Western blotting results showed that the expression level of  PAX2 protein in transfection group was increased  compared with control and empty vector groups(P<0.05);the Real-time PCR results showed that  the expression level of PAX2 mRNA  in transfection group was increased  compared with control  group and empty vector group(P<0.05).The dyeing  of E-cadherin got weaker and the dyeing of α-SMA got stronger  in transfection group compared with control and  empty vector groups. The Western blotting results showed that the expression level of E-cadherin in transfection group was decreased and α-SMA was increased  compared with control and empty vector groups (P<0.05).The Real-time PCR results showed that the expression level of E-cadherin mRNA in transfection group was decreased and the expression level of α-SMA mRNA was increased in transfection group  compared with control and empty vector groups (P<0.05). Conclusion PAX2 transfection can reduce E-cadherin expression and increase α-SMA  expression. PAX2 may  induce renal tubular mesenchymal transition in vitro.

Key words: paired box gene 2, renal tubular epithelial cells, transition, gene transfer

中图分类号: 

  • Q279