Advances in slit diaphragm signaling

被引:36
作者
New, Laura A. [1 ]
Martin, Claire E. [1 ]
Jones, Nina [1 ]
机构
[1] Univ Guelph, Dept Mol & Cellular Biol, Guelph, ON N1G 2W1, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
actin cytoskeleton; nephrin; phosphorylation; podocyte; slit diaphragm; PODOCYTE PROTEIN; TYROSINE PHOSPHORYLATION; NEPHRIN PHOSPHORYLATION; ACTIN CYTOSKELETON; CYTOPLASMIC DOMAIN; APKC-LAMBDA/IOTA; MOUSE PODOCYTES; CELL MORPHOLOGY; RHO-GTPASES; N-WASP;
D O I
10.1097/01.mnh.0000447018.28852.b6
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Purpose of review The podocyte slit diaphragm is a fundamental component of the glomerular filtration barrier and its function is highly dependent on the maintenance of specialized actin-based projections known as foot processes. In this review, we update the function of key slit diaphragm-associated proteins, and introduce some new players and emerging avenues of research within podocyte biology. Recent findings Studies using rodent models continue to support the long-held belief that precise regulation of actin dynamics at the slit diaphragm is essential for proper foot process organization. However, it is also becoming increasingly clear that alterations in actin remodeling can significantly contribute to damage in both animal models and human disease. In particular, the importance of signaling via the Rho family of GTPases has been recognized, as well as the requirement for proper localization and turnover of the slit diaphragm. Summary Regulation of the connection between the slit diaphragm and the podocyte actin network requires complex interplay between multiple signaling pathways. New discoveries contribute to an ever-expanding view of the slit diaphragm and serve to create a framework for the development of new therapeutic strategies targeting podocyte function in the future.
引用
收藏
页码:420 / 430
页数:11
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