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活性氧介导醛固酮诱导的足细胞凋亡 被引量:2

Role of reactive oxygen species in podocytes apoptosis induced by aldosterone
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摘要 目的 观察醛固酮(ALD)及其受体拮抗剂螺内酯(SPI)对足细胞活性氧(ROS)产生及凋亡的影响,并探讨其可能机制.方法 体外培养条件的永生化小鼠足细胞系,分为空白对照组、ALD组、SPI组、ALD+SPI组;用荧光分光光度计检测足细胞内ROS水平;间接免疫荧光检测nephrin表达;流式细胞仪检测足细胞凋亡率;RT-PCR、Western印迹法检测bax、bcl-2 mRNA及蛋白表达.同时观察抗氧化剂N-乙酰半胱氨酸(NAC)对上述效应的阻断作用.结果 与对照组相比,ALD诱导足细胞ROS产生增多(P<0.05),该作用可被SPI阻断(P<0.05).ALD可诱导足细胞nephrin表达降低及足细胞凋亡(P<0.05),同时伴有bax mRNA、蛋白表达升高及bcl-2 mRNA、蛋白表达降低(P<0.05),SPI及NAC可阻断这一变化(P<0.05).结论 ALD通过ROS途径作用于盐皮质激素受体上调促凋亡因子bax表达,下调抑凋亡因子bcl-2表达,进而诱导足细胞凋亡. Objective To access the effects of aldosterone (ALD) and its receptor antagonist- spironolactone (SPI) on the production of reactive oxygen species (ROS) and apoptosis in podocytes and to explore the possible mechanism involved. Methods Conditionally immortalized mouse podocytes were divided into control group, ALD group, SPI group and SPI +ALD group. The level of ROS production and the expression of nephrin protein were assayed by fluorescent spectrophotometry and indirect immunofluorescence technology. The apoptosis rate of podocytes was monitored by flow cytometry. The expression of bax and bcl-2 mRNA and protein was detected by RT-PCR and Western blotting methods. The anti-oxidant N-acetylcysteine (NAC)was applied to determine whether the effects of ALD on podocytes were mediated by ROS pathway.Results Compared with the control group, ALD significantly increased ROS production in podocytes (P〈0.05). SPI completely abolished the above-mentioned effect of ALD (P〈0.05). ALD induced the down-regulation of the expression of nephrin and the up-regulation of podocytes apoptosis (P〈0.05), which was accompanied with the elevated expression of bax mRNA and protein and the reduced expression of bcl-2 mRNA and protein (P〈0.05). SPI or NAC prevented the above-mentioned changes induced by ALD (P〈0.05). Conclusion ALD increases theexpression of pro-apoptotic factor (bax) but decreases the expression of anti-apoptotic factor (bcl-2)to induce podocytes apoptosis through the mineralocorticoid receptor (MR) possibly via the mechanisms involving ROS pathway.
出处 《中华肾脏病杂志》 CAS CSCD 北大核心 2010年第9期678-682,共5页 Chinese Journal of Nephrology
基金 国家自然科学基金(30871174,30500245) 湖北省卫生厅科研基金(NX200510)
关键词 足细胞 醛固酮 活性氧 细胞凋亡 Podoeytes Aldosterone Reactive oxygen species Apoptosis
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参考文献14

  • 1Patni H,Mathew JT,Luan L,et al.Aldosterone promotes proximal tubular cell apoptosis:role of oxidative stress.Am J Physiol Renal Physiol,2007,293:F1065-F1071.
  • 2Mathew JT,Patni H,Chaudhary AN,et al.Aldosterone induces mesangial cell apoptosis both in vivo and in vitro.Am J Physiol Renal Physiol,2008,295:F73-F81.
  • 3Nishikawa T,Suematsu S,Saito J,et al.Human renal mesangial cells produce aldosterone in response to lowdensity lipoprotein (LDL).J Steroid Biochem Mol Biol,2005,96:309-316.
  • 4Nagase M,Fujita T.Aldosterone and glomerular podocyte injury.Clin Exp Nephrol,2008,12:233-242.
  • 5Shankland SJ,Pippin JW,Reiser J,et al.Podocytes in culture:past,present,and future.Kidney Int,2007,72:26-36.
  • 6姜华军,张春,朱忠华,刘建社,邓安国.CD2相关蛋白在肾脏固有细胞中的表达及分布[J].中华肾脏病杂志,2007,23(6):404-405. 被引量:5
  • 7Connell JM,Davies E.The new biology of aldosterone.J Endocrinol,2005,186:1-20.
  • 8Chuang PY,He JC.Signaling in regulation of podocyte phenotypes.Nephron Physiol,2009,111:9-15.
  • 9Foster RR,Saleem MA,Mathieson PW,et al.Vascular endothelial growth factor and nephrin interact and reduce apoptosis in human podocytes.Am J Physiol Renal Physiol,2005,288:F48-F57.
  • 10Whaley-Connell A,Habibi J,Wei Y,et al.Mineralocorticoid receptor antagonism attenuates glomerular filtration barrier remodeling in the transgenic Ren2 rat.Am J Physiol Renal Physiol,2009,296:F1013-F1022.

二级参考文献7

  • 1Shih NY, Li J, Karpitskii V, et al. Congenital nephritic syndrome in mice lacking CD2-associated protein. Science, 1999, 286(5438): 312-315.
  • 2Shih NY, Li J, Cotran R, et al. CD2AP localizes to the slit diaphragm and binds to nephrin via a novel c-terminal domain. Am J Pathol, 2001, 159: 2303-2308.
  • 3Lehtonen S, Zhao F, Lehtonen E. CD2-associated protein directly interacts with the actin cytoskeleton. Am J Physiol Renal Physiol, 2002, 283: F734-F743.
  • 4Mundel P, Reiser J, Borja AZ, et al. Rearrangements of the cytoskeleton and cell contacts induce process formation during differentiation of conditionally immortalized mouse podocyte cell lines. Exp Cell Res, 1997, 236: 248-258.
  • 5Smoyer WE, Mundel P. Regulation of podocyte structure during the development of nephritic syndrome. J Mol Med, 1998, 76: 172-183.
  • 6Saleem MA, Ni L, Witherden L, et al. Co-localization of nephfin, podocin, and the actin cytoskeleton. Am J Pathol, 2002, 161: 1459-1466.
  • 7Coward RJM, Foster RR, Patton D, et al. Nephrotic plasma alters slit diaphragm-dependent signaling and translo cates nephrin, podocin, and CD2-associated protein in cultured human podoeytes. J Am Soc Nephrol, 2005, 16: 629-637.

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