Fan Qingfeng, Xing Yan, Ding Jie, Guan Na
Department of Pediatrics, Peking University First Hospital, Beijing, PR China.
Nephron Exp Nephrol. 2009;111(4):e92-e102. doi: 10.1159/000209209. Epub 2009 Mar 17.
BACKGROUND/AIMS: The relationship between vascular endothelial growth factor (VEGF) and the phosphorylated critical podocyte slit diaphragm molecule nephrin is not fully clarified. This study investigated the dynamic changes in VEGF expression and nephrin phosphorylation, and the effects of the antiproteinuric drugs prednisone and lisinopril on them in Adriamycin nephropathy rats.
Renal tissues from Adriamycin rats were collected at days 3, 7, 14, and 28. Distribution and expression of VEGF was revealed by immunohistochemistry, real-time PCR and Western blot. Phosphorylated nephrin was evaluated by immunoprecipitation.
A discontinuous redistribution of VEGF was displayed at day 3, followed by significant protein reduction at day 7 with persistent downregulation to day 28. Phosphorylated nephrin decreased evidently at day 14 and persisted to day 28. The reduction in VEGF and phosphorylated nephrin was not a result of podocyte loss. The intervention of prednisone and lisinopril evidently reduced proteinuria, effectively attenuated the severe lesions of podocyte foot processes, and restored the reduction in VEGF and nephrin phosphorylation. At day 28, the reduction in VEGF and phosphorylated nephrin was negatively correlated with proteinuria, whereas the phosphorylated nephrin was positively correlated with VEGF protein from day 7 to day 28.
The reduction in VEGF protein and nephrin phosphorylation was possibly involved in the proteinuria in Adriamycin rats, and there might be some relationship between VEGF and nephrin phosphorylation. The antiproteinuric effects of lisinopril and prednisone were achieved at least partially by restoring VEGF protein and nephrin phosphorylation.
背景/目的:血管内皮生长因子(VEGF)与关键足细胞裂孔隔膜分子nephrin的磷酸化之间的关系尚未完全阐明。本研究调查了阿霉素肾病大鼠中VEGF表达和nephrin磷酸化的动态变化,以及抗蛋白尿药物泼尼松和赖诺普利对它们的影响。
在第3、7、14和28天收集阿霉素大鼠的肾组织。通过免疫组织化学、实时PCR和蛋白质印迹法揭示VEGF的分布和表达。通过免疫沉淀评估磷酸化的nephrin。
VEGF在第3天出现不连续的重新分布,随后在第7天蛋白质显著减少,并持续下调至第28天。磷酸化的nephrin在第14天明显减少,并持续到第28天。VEGF和磷酸化nephrin的减少不是足细胞丢失的结果。泼尼松和赖诺普利的干预明显减少了蛋白尿,有效减轻了足细胞足突的严重病变,并恢复了VEGF和nephrin磷酸化的减少。在第28天,VEGF和磷酸化nephrin的减少与蛋白尿呈负相关,而从第7天到第28天,磷酸化nephrin与VEGF蛋白呈正相关。
VEGF蛋白和nephrin磷酸化的减少可能与阿霉素大鼠的蛋白尿有关,并且VEGF和nephrin磷酸化之间可能存在某种关系。赖诺普利和泼尼松的抗蛋白尿作用至少部分是通过恢复VEGF蛋白和nephrin磷酸化来实现的。