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血管内皮生长因子与糖尿病肾病的足细胞。

VEGF and podocytes in diabetic nephropathy.

机构信息

Department of Pediatrics, Section of Nephrology, Yale University School of Medicine, New Haven, CT 06520-8064, USA.

出版信息

Semin Nephrol. 2012 Jul;32(4):385-93. doi: 10.1016/j.semnephrol.2012.06.010.

Abstract

Vascular endothelial growth factor-A (VEGF-A) is a protein secreted by podocytes that is necessary for survival of endothelial cells, podocytes, and mesangial cells. VEGF-A regulates slit-diaphragm signaling and podocyte shape via VEGF-receptor 2-nephrin-nck-actin interactions. Chronic hyperglycemia-induced excess podocyte VEGF-A and low endothelial nitric oxide drive the development and the progression of diabetic nephropathy. The abnormal cross-talk between VEGF-A and nitric oxide pathways is fueled by the diabetic milieu, resulting in increased oxidative stress. Recent findings on these pathogenic molecular mechanisms provide new potential targets for therapy for diabetic renal disease.

摘要

血管内皮生长因子-A(VEGF-A)是一种由足细胞分泌的蛋白质,对于内皮细胞、足细胞和系膜细胞的存活是必需的。VEGF-A 通过 VEGF 受体 2-nephrin-nck-actin 相互作用调节裂孔隔膜信号和足细胞形状。慢性高血糖诱导的过量足细胞 VEGF-A 和低内皮一氧化氮驱动糖尿病肾病的发生和进展。VEGF-A 和一氧化氮通路之间的异常串扰是由糖尿病环境引起的,导致氧化应激增加。这些致病分子机制的最新发现为糖尿病肾病的治疗提供了新的潜在靶点。

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