Vascular Growth Factors and Glomerular Disease

被引:96
作者
Bartlett, Christina S. [1 ,2 ]
Jeansson, Marie [3 ]
Quaggin, Susan E. [1 ,2 ]
机构
[1] Northwestern Univ, Feinberg Cardiovasc Res Inst, Chicago, IL 60611 USA
[2] Northwestern Univ, Div Nephrol & Hypertens, Chicago, IL 60611 USA
[3] Uppsala Univ, Dept Immunol Genet & Pathol, S-75185 Uppsala, Sweden
来源
ANNUAL REVIEW OF PHYSIOLOGY, VOL 78 | 2016年 / 78卷
关键词
VEGF; angiopoietin; podocyte; endothelial cell; RECEPTOR TYROSINE KINASE; ENDOTHELIAL-CELL SURVIVAL; AUTOCRINE VEGF-A; MESANGIAL CELL; TIE2; RECEPTOR; RENAL EXPRESSION; MICE DEFICIENT; BLOOD-VESSELS; MESSENGER-RNA; IN-VITRO;
D O I
10.1146/annurev-physiol-021115-105412
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The glomerulus is a highly specialized microvascular bed that filters blood to form primary urinary filtrate. It contains four cell types: fenestrated endothelial cells, specialized vascular support cells termed podocytes, perivascular mesangial cells, and parietal epithelial cells. Glomerular cell-cell communication is critical for the development and maintenance of the glomerular filtration barrier. VEGF, ANGPT, EGF, SEMA3A, TGF-beta, and CXCL12 signal in paracrine fashions between the podocytes, endothelium, and mesangium associated with the glomerular capillary bed to maintain filtration barrier function. In this review, we summarize the current understanding of these signaling pathways in the development and maintenance of the glomerulus and the progression of disease.
引用
收藏
页码:437 / 461
页数:25
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