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血管紧张素Ⅱ灌注诱导nephrin表达改变与足细胞凋亡
引用本文:贾俊亚,朱吉莉,丁国华,陈铖,梁伟,杨红霞.血管紧张素Ⅱ灌注诱导nephrin表达改变与足细胞凋亡[J].中华肾脏病杂志,2007,23(1):33-38.
作者姓名:贾俊亚  朱吉莉  丁国华  陈铖  梁伟  杨红霞
作者单位:武汉大学人民医院肾内科,430060
基金项目:国家自然科学基金(30370656);湖北省卫生厅重点科研项目(JXIB011)
摘    要:目的 研究血管紧张素Ⅱ(AngⅡ)灌注对大鼠足细胞裂隙膜分子nephrin表达及足细胞凋亡的影响,以及探讨AngⅡ引起蛋白尿及肾小球硬化的机制。方法 36只雄性Sprague Dawley大鼠分为AngⅡ灌注组(400 ng&#8226;kg-1&#8226;min-1)、生理盐水灌注组和正常对照组,测定28 d内大鼠血压及尿蛋白。分别于14、28 d处死动物取肾,观察组织学改变,并用免疫荧光、免疫电镜检测nephrin分布。RT-PCR及Western印迹法分别检测nephrin mRNA及蛋白表达。TUNEL法检测足细胞凋亡。结果 (1) AngⅡ灌注组大鼠血压升高,14 d达峰值并维持该水平至28 d;AngⅡ灌注7 d即出现蛋白尿,并持续增加。(2) AngⅡ灌注14 d时,足细胞裂隙膜变窄;灌注28 d时,足突增宽及节段性融合,部分足细胞有凋亡小体形成,少数肾小球出现节段性硬化。TUNEL法检测发现足细胞凋亡(2.7±1.6)个/肾小球切面],凋亡数与蛋白尿量呈正相关(r = 0.86,P < 0.01)。(3) AngⅡ灌注14 d时,肾皮质nephrin mRNA及蛋白表达上调(P < 0.05)。nephrin由正常的沿毛细血管袢线状分布向粗颗粒、团块状分布模式转变。AngⅡ灌注28 d时,肾皮质nephrin mRNA及蛋白表达下降(P < 0.05),且nephrin蛋白表达与足细胞凋亡数呈负相关(r = -0.63,P < 0.01)。 结论 AngⅡ灌注诱导的nephrin表达及分布改变可能导致了足细胞凋亡及肾小球硬化的发生与发展。

关 键 词:血管紧张素Ⅱ蛋白尿Nephrin足细胞凋亡
收稿时间:2006-7-19
修稿时间:2006-07-19

Angiotensin Ⅱ infusion induces nephrin expression change and podocyte apoptosis
JIA Jun-ya,ZHU Ji-li,DING Guo-hua,CHEN Cheng,LIANG Wei,YANG Hong-xia.Angiotensin Ⅱ infusion induces nephrin expression change and podocyte apoptosis[J].Chinese Journal of Nephrology,2007,23(1):33-38.
Authors:JIA Jun-ya  ZHU Ji-li  DING Guo-hua  CHEN Cheng  LIANG Wei  YANG Hong-xia
Institution:Division of Nephrology, Renmin Hospitol, Wuhan University, Wuhan 430060, China
Abstract:Objective To evaluate the effects of angiotensin II (Ang II) infusion on nephrin expression and podocyte apoptosis in vivo, and investigate the mechanism of proteinuria and glomerulosclerosis induced by Ang II infusion. Methods Thirty-six male Sprague-Dawley rats were randomly assigned to receive either normal saline or Ang II (400 ng&#8226;kg-1&#8226;min-1) by osmotic mini-pump, or to be used as normal control. After the systolic blood pressure was measured, the 24 h urine sample was collected for analysis of proteinuria at day 7, 14, 21, 28. Animals were sacrificed at day 14, 28 respectively. Serum creatinine, renal pathological change, podocyte apoptosis were observed. Expression of nephrin mRNA and protein was examined by RT-PCR, Western blot, and immunofluorescence staining. Results (1) Ang II-infused rats developed significant hypertension associated with marked proteinuria. Significantly positive correlation was found between blood pressure and proteinuria (r = 0.80,P < 0.01). (2)At day 14, Ang II infusion induced the narrowing of slit diaphragm. At day 28, apoptotic podocytes were detected by electron microscopy and TUNEL assay (2.7±1.6) apoptotic podocytes per glomerular cross section] in Ang II-infused rats. (3) Distribution of nephrin expression was changed from linear to granular pattern in Ang II-infused rats at day 14 and expression of nephrin mRNA and protein increased (P < 0.05). But at day 28, expression of nephrin mRNA and protein was decreased, and significantly negative correlation was found between the expression of nephrin and the number of apoptotic podocytes (r = 0.63,P < 0.01). Conclusion Change in nephrin expression may play a critical role in the pathogenesis of Ang II-induced podocyte apoptosis.
Keywords:Angiotensin II  Proteinuria  Nephrin  Podocyte  Apoptosis
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