| Literature DB >> 26084928 |
Kazunori Inoue1, Shuta Ishibe2.
Abstract
Severe defects in the glomerular filtration barrier result in nephrotic syndrome, which is characterized by massive proteinuria. The podocyte, a specialized epithelial cell with interdigitating foot processes separated by a slit diaphragm, plays a vital role in regulating the passage of proteins from the capillary lumen to Bowman's space. Recent findings suggest a critical role for endocytosis in podocyte biology as highlighted by genetic mouse models of disease and human genetic mutations that result in the loss of the integrity of the glomerular filtration barrier. In vitro podocyte studies have also unraveled a plethora of constituents that are differentially internalized to maintain homeostasis. These observations provide a framework and impetus for understanding the precise regulation of podocyte endocytic machinery in both health and disease.Entities:
Keywords: endocytosis; glomerular disease; phosphoinositides; podocyte
Mesh:
Year: 2015 PMID: 26084928 PMCID: PMC4556893 DOI: 10.1152/ajprenal.00136.2015
Source DB: PubMed Journal: Am J Physiol Renal Physiol ISSN: 1522-1466