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VEGF_(165)抑制HK2细胞上皮-间充质转化过程中NOTCH信号系统的变化 被引量:5

Down-regulation of NOTCH signaling system in the inhibition of epithelial-mesenchymal transition (EMT) by VEGF_(165) in HK2 cells
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摘要 目的探讨应用血管内皮生长因子(VEGF165)干预肾小管上皮-间充质转化(EMT)过程中NOTCH信号系统的变化及其意义。方法(1)体外培养的人肾小管上皮细胞(HK2)分为转化生长因子-β1(TGF-β1,5μg/L)单独作用组(T组)和TGF-β1(5μg/L)+VEGF(100μg/L)共同作用组(T+V组),RT-PCR及Western blot方法检测不同作用时间点JAGGED-1、α-平滑肌肌动蛋白(α-SMA)的表达。(2)TGF-β1与不同浓度VEGF165(0.1、1、10和100μg/L)共同作用细胞24 h,激光共聚焦显微镜(CFMS)、RT-PCR及Western blot检测E-钙黏素、α-SMA、JAGGED-1、NOTCH1表达。结果(1)作用后24和48 h,T+V组α-SMA和JAGGED-1蛋白表达均明显低于T组(P<0.05)。(2)同TGF-β1单独作用组比较,VEGF165(100μg/L)与TGF-β1共同作用组的E-钙黏素表达明显增强,α-SMA、JAGGED-1及NOTCH1表达均明显降低(P<0.05)。结论VEGF可抑制TGF-β1诱导HK2细胞发生EMT,并同时下调EMT过程中JAGGED-1、NOTCH1分子表达,提示该效应可能是VEGF抑制EMT的机制之一。 Objective To examine the effect of VEGF165 on expressions of JAGGED-1 and NOTCH1 and the relationship between these expressions and epithelial-mesenchymal transition(EMT) induced by TGF-β1.MethodsCultured HK2 cells were incubated with TGF-β1(5 μg/L) in the absence(group T) or presence(group T+V) of VEGF165(100 μg/L),respectively.Expressions of α-SMA and JAGGED-1 mRNA were assessed with RT-PCR and the protein expressions were assessed with Western blot at different time points,respectively.In the other experiment,HK2 cells were divided into four groups: negative control,incubated with TGF-β1(5 μg/L) along,with VEGF165(100 μg/L) along,or with TGF-β1(5 μg/L) and VEGF165 at different concentrations(0.1,1,10,100 μg/L) for 24 hours.Confocal microscope was used to detect expressions of α-SMA and E-cadherin.Protein and mRNA expressions of α-SMA,JAGGED-1 and NOTCH1 were assessed with RT-PCR and Western blot,respectively.Results Protein expression of both α-SMA and JAGGED-1 significantly decreased in group T+V at 24 and 48 h as compared with group T(P0.05).VEGF165 reversed TGF β1-induced inhibition of E-cadherin and promotion of α-SMA,JAGGED-1 and NOTCH1 significantly(P0.05).Conclusion The results of the present study showed that VEGF165 may partially inhibit TGF-β1 induced EMT of HK2 cells in vitro,which is probably contributed to the repression of JAGGED-1 and NOTCH1 expressions.
出处 《基础医学与临床》 CSCD 北大核心 2010年第10期1029-1036,共8页 Basic and Clinical Medicine
基金 国家自然科学基金(30570854)
关键词 血管内皮生长因子 上皮-间充质转化 JAGGED-1 NOTCH1 vascular endothelial growth factor(VEGF) epithelial-mesenchymal transition(EMT) JAGGED-1 NOTCH1
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  • 1周秋根,郑法雷,文煜冰,谭小月,段林,李艳.人肾小管上皮细胞转分化过程中血管内皮细胞生长因子及其受体表达的变化[J].中国医学科学院学报,2005,27(3):325-331. 被引量:8
  • 2Oft M, Akhurst RJ, Balmain A. Metastasis is driven by sequential elevation of H-ras and Smad2 levels. Nat Cell Biol 2002; 4:487-494.
  • 3Takano S, Kanai F, Jazag A, et al. Smad4 is essential for down-regulation of E-cadherin induced by TGF-β in pancreatic cancer cell line PANC-1. JBiochem 2007; 141:345-351.
  • 4Kaimori A, Potter J, Kaimori JY, et al. Transforming growth factor-β1 induces an epithelial-to-mesenchymal transition state in mouse hepatocytes in vitro. J Biol Chem 2007; 282:22089-22101.
  • 5Bardeesy N, Cheng KH, Berger JH, et al. Smad4 is dispensable for normal pancreas development yet critical in progres- sion and tumor biology of pancreas cancer. Genes Dev 2006; 20:3130-3146.
  • 6Desgrosellier JS, Mundell NA, McDonnell MA, Moses HL, Barnett JV. Activin receptor-like kinase 2 and Smad6 regulate epithelial-mesenchymal transformation during cardiac valve formation. Dev Biol 2005; 280:201-210.
  • 7Armstrong E J, Bischoff J. Heart valve development: endothelial cell signaling and differentiation. Circ Res 2004; 95:459- 470.
  • 8Saika S, Ikeda K, Yamanaka O, et al. Transient adenoviral gene transfer of Smad7 prevents injury-induced epithelialmesenchymal transition of lens epithelium in mice. Lab Invest 2004; 84:1259-1270.
  • 9Xu GP, Li QQ, Cao XX, et al. The fffect of TGF-β1 and SMAD7 gene transfer on the phenotypic changes of rat al- veolar epithelial cells. Cell Mol Biol Lett 2007; 12:457-472.
  • 10Dooley S, Hamzavi J, Ciuclan L, et al. Hepatocyte-specific Smad7 expression attenuates TGF-β-mediated fibrogenesis and protects against liver damage. Gastroenterology 2008; 135:642-659.

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  • 1周秋根,郑法雷,文煜冰,谭小月,段林,李艳.人肾小管上皮细胞转分化过程中血管内皮细胞生长因子及其受体表达的变化[J].中国医学科学院学报,2005,27(3):325-331. 被引量:8
  • 2周斌,张培建.胆管上皮细胞的生理及其与胆管疾病的相关性[J].中国普通外科杂志,2007,16(7):681-683. 被引量:9
  • 3王启明,贾连群,周鸿鹰,李云生.Wnt/β-catenin信号因子在HepG2以及L02细胞中的表达[J].细胞与分子免疫学杂志,2007,23(10):926-928. 被引量:8
  • 4Greenburg G,Hay ED. Epithelia suspended in col-lagengels can lose polarity and express characteris-tics of migrating mesenchymal cells[J]. J Cell Biol,1982, 95(1): 333 — 339.
  • 5Kalluri R, Weinberg RA. The basics of epithelial-mesenchymal transition [J]. J Clin Invest, 2009,119(6): 1420-1428.
  • 6Wendt MK,Allington TM, Schiemann WP. Mech-anisms of the epithelial-mesenchymal transition byTGF-beta[J]. Future Oncol, 2009 . 5(8): 1145 —1168.
  • 7Barrallo-Gimeno A, Nieto MA, The Snail genes asinducers of cell movement and survival : Implicationsin development and cancer[J]. Development, 2005.132(14) : 3151-3161.
  • 8Gonzalez-Moreno 〇,Lecanda J, Green JE, et al.VEGF elicits epithelial-mesenchymal transition(EMT) in prostate intraepithelial neoplasia (PIN)-like cells via an autocrine loop [J]. Exp Cell Res,2010,316(14) : 554-567.
  • 9Cho HJ, Baek KE, Saika S,et al. Snail is requiredfor transforming growth factor-beta induced epithe-lial-mesenchymal transition by activating PI3 ki-nase/ Aktsignal pathway[J]. Biochem Biophys ResCommun, 2007 . 353(2) : 337 — 343.
  • 10Xu SY,Li J,Geng MY. The signal transductionand drug development of epithelial-mesenchymaltransition[J]. Chin Pharmacol Bull, 2008,24(9):1131-1134.

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