Regulation of the Actin Cytoskeleton in Podocytes

被引:90
|
作者
Blaine, Judith [1 ]
Dylewski, James [1 ,2 ]
机构
[1] Univ Colorado, Renal Div, Anschutz Med Campus, Aurora, CO 80045 USA
[2] Denver Hlth Med Ctr, Aurora, CO 80045 USA
关键词
podocyte; actin cytoskeleton; foot process; slit diaphragm; focal adhesion; GLOMERULAR-FILTRATION BARRIER; PUROMYCIN AMINONUCLEOSIDE NEPHROSIS; FOCAL SEGMENTAL GLOMERULOSCLEROSIS; NEPHRIN TYROSINE PHOSPHORYLATION; CELL-MATRIX ADHESION; SLIT DIAPHRAGM; TRPC6; CHANNELS; ANGIOTENSIN-II; GROWTH-FACTOR; HIGH GLUCOSE;
D O I
10.3390/cells9071700
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Podocytes are an integral part of the glomerular filtration barrier, a structure that prevents filtration of large proteins and macromolecules into the urine. Podocyte function is dependent on actin cytoskeleton regulation within the foot processes, structures that link podocytes to the glomerular basement membrane. Actin cytoskeleton dynamics in podocyte foot processes are complex and regulated by multiple proteins and other factors. There are two key signal integration and structural hubs within foot processes that regulate the actin cytoskeleton: the slit diaphragm and focal adhesions. Both modulate actin filament extension as well as foot process mobility. No matter what the initial cause, the final common pathway of podocyte damage is dysregulation of the actin cytoskeleton leading to foot process retraction and proteinuria. Disruption of the actin cytoskeleton can be due to acquired causes or to genetic mutations in key actin regulatory and signaling proteins. Here, we describe the major structural and signaling components that regulate the actin cytoskeleton in podocytes as well as acquired and genetic causes of actin dysregulation.
引用
收藏
页码:1 / 27
页数:27
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