期刊文献+

嘌呤霉素损伤小鼠肾小球足细胞系中podocin表达与分布的影响及其意义 被引量:3

Distribution and Expression of Podocin in Puromycin Aminonucleoside Injured Mouse Podocyte Cell Line
原文传递
导出
摘要 目的Podocin是构成肾小球足细胞裂孔隔膜(slit diaphragm,SD)完整性的重要分子,其表达异常与大量蛋白尿的形成有关。本研究采用体外培养肾小球足细胞系,探讨足细胞损伤过程中,podocin mRNA表达和分布变化与足细胞损伤的关系。方法将体外培养的足细胞采用随机数字表法设立为实验组与对照组。实验组采用嘌呤霉素(puromycin aminonucleoside,PAN)刺激(剂量为50μg/mL),分别于8 h,24 h和48 h观察细胞形态、提取总RNA和细胞免疫组化观察podocin的分布。对照组用含10%FBS的RPMI 1640培养液培养。细胞图像应用Image J图像处理软件,计算实验组与对照组在上述各时间点200倍镜下随机选择的30个细胞的相对面积,半定量RT-PCR和间接免疫荧光法检测podocin mRNA表达和分布变化。结果对照组呈星形伸出树枝状突起,相邻细胞间形成相互连接。实验组细胞体缩小,足突回缩、消失,细胞间失去相互连接。上述各时间点两组间podocin mRNA表达比较,差异无显著意义(P>0.05)。Podocin在对照组呈细丝状均匀分布于细胞核膜、细胞质及细胞膜;在实验组主要沿细胞核膜呈点线样分布,刺激后8 h和24 h细胞质有少许分布,刺激48 h后出现细胞膜、细胞质分布缺失。结论Podocin分布异常与足细胞损伤密切相关,损伤早期即有变化;podocin分布异常是足细胞损伤过程中的重要分子效应。 Objective To explore the podocin mRNA expression and distribution in a time series scale in the couse of podocyte injury in vitro. Methods Mouse podocyte cell line (MPCS) were regenerated at 33℃ for proliferation in the presence of Y-inferon, and then subcultured at 37℃ without 7-inferon for differentiation about 8 - 10 days, which would be subsequently subject to puromycin aminonucleoside (PAN) treatment. The podocyte morphology was observed by the phase contrast microscope. The podocin mRNA expression level and distribution were examined by indirect immunocytofluorescence, semi-quantitative RT-PCR at 8 h, 24 h, and 48 h, respectively. Results (1)The well-developed podocyte arborization was formed after the in vitro induction,the PAN treatment led to the podocyte foot processe retraction and effacement together with the MPC5 shrinkage and the loss of cell contact. (2) Podocin was evenly distributed in a filamentous pattern with the small dots across the well- differentiated MPCS, which was shifted to an uneven, discontinuous coarse puncta limited in the nuclei immediately after PAN treatment. (3) Semi-quantitative RT-PCR found that mRNA level had no significant changes after PAN treatment (P〉0. 05); however, immunocytochemistry suggested podocin disappeared in the cellular membrane and cytoplasm significantly (P〈0.05). Conclusion Because of the intimate concomitance, the changed distribution pattern of podocin was the prominent effect of the podocyte injury, which might be related to the disease mechanism.
出处 《中华妇幼临床医学杂志(电子版)》 CAS 2008年第5期8-11,共4页 Chinese Journal of Obstetrics & Gynecology and Pediatrics(Electronic Edition)
基金 广东省自然科学基金项目(5000424) 广东省科技计划项目(2005B36001019) 广州市科技攻关计划项目资助(2006Z3-E0231)~~
关键词 足细胞系 PODOCIN 嘌呤霉素 podocyte cell line podocin puromycin aminonucleoside(PAN)
  • 相关文献

参考文献3

二级参考文献52

  • 1范青锋,丁洁,张敬京,管娜,邓江红.podocin基因敲低对小鼠足细胞nephrin和α-actinin表达与分布的影响[J].中华肾脏病杂志,2004,20(5):325-329. 被引量:4
  • 2秦卫松,刘志红,曾彩虹,郑春霞,贾忠辉,王生余,黎磊石.雷公藤甲素对Heymann肾炎模型足细胞病变的影响[J].肾脏病与透析肾移植杂志,2007,16(2):101-109. 被引量:97
  • 3郑春霞,刘志红,孙吉平,曾彩虹,王生余,黎磊石.雷公藤甲素对嘌呤霉素模型足细胞病变的影响[J].肾脏病与透析肾移植杂志,2007,16(2):110-118. 被引量:37
  • 4黎磊石 张训.雷公藤治疗肾小球肾炎的临床研究[J].中华内科杂志,1981,20:216-216.
  • 5黎磊石 张训(等).雷公藤治疗肾小球肾炎的临床与实验研究[J].中华医学杂志,1982,62:581-581.
  • 6Kestila M,Lenkkeri U,Mannikko M,et al.Positionally cloned gene for a novel glomerular protein nephrin is mutated in congenital nephrotic syndrome.J Mol Cell,1998,1:575-582.
  • 7Boute N,Gribouval O,Roselli S,et al.NPHS2,encoding the glomerular protein podocin,is mutated in autosomal recessive steroid-resistant nephritic syndrome.Nat Genet,2000,24:349-354.
  • 8Shih NY,Li J,Karpitskii V,et al.Congenital nephrotic syndrome in mice lacking CD2-associated protein.Science,1999,286:312-315.
  • 9Kaplan JM,Kim SH,North KN,et al.Mutations in ACTN4,encoding α-actinin-4,cause familial focal segmental glomerulosclerosis.Nat Genet,2000,24:251-256.
  • 10Patrakka J,Ruotsalainen V,Ketola I,et al.Expression of nephrin in pediatric kidney diseases.J Am Soc Nephrol,2001,12:289-296.

共引文献95

同被引文献23

  • 1周伟,陈楠,潘晓霞,张文,徐耀文,王伟铭,王朝晖.肾病综合征患者肾组织podocin的表达[J].中华肾脏病杂志,2005,21(9):502-505. 被引量:16
  • 2邢燕,丁洁,范青锋,管娜.足细胞分子高表达致阿霉素肾病大鼠发生蛋白尿[J].中华肾脏病杂志,2006,22(1):27-32. 被引量:39
  • 3Koop K, Eikmans M, Baelde HJ, et ol. Expression of podoeyte-assoeiated molecules in acquired human kidney diseases [J]. J Am Soc Nephrol,2003 14(8):2063-2071.
  • 4Xing Y, Ding J, Fan Q, et al. Diversities of podocyte molecular changes induced by different antiproteinuria drugs [J]. Exp Biol Med,2006,231 (5):585-593.
  • 5Shibata S, Nagase M, Fujita T. Fluvastatin ameliorates podocyte injury in proteinuric rats via modulation of excessive Rho signaling [J]. J Am Soc Nephrol,2006,17 (3) :754-764.
  • 6Roselli S, Heidet L, Sich M, et al. Early glomerular filtration defect and severe renal disease in podocindeficient mice [J]. Mol Cell Biol,2004,24(2) :550-560.
  • 7Fan Q, Xing Y, Ding J, et ol. The relationship among nephrin, podocin, CD2AP, and alpha-actinin might not be a true "interaction" in podocyte [J]. Kidney Int,2006, 69(7) : 1207-1215.
  • 8Ruf RG, Lichtenberger A, Karle SM, et al. Patients with mutations in NPHS2(podocin) do not respond to standard steroid treatmet of nephrotic syndrome [J].J Am Soc Nephrol, 2004,15 (3) : 722-732.
  • 9Mao J, Zhang Y, Du L, et al. NPHS1 and NPHS2 gene mutations in Chinese children with sporadic nephrotic syndrome[J]. Pediatr Res, 2007,61 ( 1 ) : 117-122.
  • 10Yu B,Sun X,Shen HY,et al.Expression of the apoptosis-related genes BCL-2 and BAD in human breast carcinoma and their associated relationship with chemosensitivity[J].J Exp Clin Cancer Res,2010,29(1):107.

引证文献3

二级引证文献13

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部