Dynamic (re)organization of the podocyte actin cytoskeleton in the nephrotic syndrome

被引:125
作者
Oh, J
Reiser, J
Mundel, P
机构
[1] Yeshiva Univ Albert Einstein Coll Med, Div Nephrol, Bronx, NY 10461 USA
[2] Heidelberg Univ, Childrens Hosp, Div Pediat Nephrol, D-6900 Heidelberg, Germany
[3] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Renal Unit, Boston, MA USA
关键词
podocytes; foot process effacement; proteinuria; integrins; glomerular basement membrane; dystroglycan;
D O I
10.1007/s00467-003-1367-y
中图分类号
R72 [儿科学];
学科分类号
100202 [儿科学];
摘要
The visceral glomerular epithelial cell, also known as the podocyte, plays an important role in the maintenance of renal glomerular function. This cell type is highly specialized and its foot processes together with the interposed slit diaphragm (SD) form the final barrier to urinary protein loss. Effacement of foot processes is associated with the development of proteinuria and-if not reversed in a certain time-with permanent deterioration of the glomerular filter. To maintain an intact glomerular filter barrier, podocyte-podocyte interactions and podocyte interactions with the glomerular basement membrane (GBM) are essential. Recent years have highlighted podocyte functions by unraveling the molecular composition of the SD, but have also clarified the important role of the podocyte actin cytoskeleton, and the podocyte-GBM interaction in the development of foot process (FP) effacement. This review provides an update of podocyte functions with respect to novel podocyte-specific proteins and also focuses on the dynamic interaction between the actin cytoskeleton of podocytes, their cell surface receptors and the GBM.
引用
收藏
页码:130 / 137
页数:8
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