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Regulation of the Actin Cytoskeleton in Podocytes

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 b...

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Autores principales: Blaine, Judith, Dylewski, James
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7408282/
https://www.ncbi.nlm.nih.gov/pubmed/32708597
http://dx.doi.org/10.3390/cells9071700
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author Blaine, Judith
Dylewski, James
author_facet Blaine, Judith
Dylewski, James
author_sort Blaine, Judith
collection PubMed
description 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.
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spelling pubmed-74082822020-08-13 Regulation of the Actin Cytoskeleton in Podocytes Blaine, Judith Dylewski, James Cells Review 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. MDPI 2020-07-16 /pmc/articles/PMC7408282/ /pubmed/32708597 http://dx.doi.org/10.3390/cells9071700 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Blaine, Judith
Dylewski, James
Regulation of the Actin Cytoskeleton in Podocytes
title Regulation of the Actin Cytoskeleton in Podocytes
title_full Regulation of the Actin Cytoskeleton in Podocytes
title_fullStr Regulation of the Actin Cytoskeleton in Podocytes
title_full_unstemmed Regulation of the Actin Cytoskeleton in Podocytes
title_short Regulation of the Actin Cytoskeleton in Podocytes
title_sort regulation of the actin cytoskeleton in podocytes
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7408282/
https://www.ncbi.nlm.nih.gov/pubmed/32708597
http://dx.doi.org/10.3390/cells9071700
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