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Microtubule-associated protein tau in murine kidney: role in podocyte architecture
Tau is a cytoskeletal protein that is expressed mainly in neurons and is involved in several cellular processes, such as microtubule stabilization, axonal maintenance, and transport. Altered tau metabolism is related to different tauopathies being the most important Alzheimer’s disease where aberran...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8794918/ https://www.ncbi.nlm.nih.gov/pubmed/35084555 http://dx.doi.org/10.1007/s00018-021-04106-z |
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author | Vallés-Saiz, Laura Peinado-Cahuchola, Rocio Ávila, Jesús Hernández, Félix |
author_facet | Vallés-Saiz, Laura Peinado-Cahuchola, Rocio Ávila, Jesús Hernández, Félix |
author_sort | Vallés-Saiz, Laura |
collection | PubMed |
description | Tau is a cytoskeletal protein that is expressed mainly in neurons and is involved in several cellular processes, such as microtubule stabilization, axonal maintenance, and transport. Altered tau metabolism is related to different tauopathies being the most important Alzheimer’s disease where aberrant hyperphosphorylated and aggregated tau is found in the central nervous system. Here, we have analyzed that function in kidney by using tau knockout mice generated by integrating GFP-encoding cDNA into exon 1 of MAPT (here referred to as Tau(GFP/GFP)). IVIS Lumina from PerkinElmer demonstrated GFP expression in the kidney. We then demonstrated by qPCR that the main tau isoform in the kidney is Tau4R. The GFP reporter allowed us to demonstrate that tau is found in the glomeruli of the renal cortex, and specifically in podocytes. This was further confirmed by immunohistochemistry. Tau(GFP/GFP) mice present a podocyte cytoskeleton more dynamic as they contain higher levels of detyrosinated tubulin than wild-type mice. In addition, transmission electron microscopy studies demonstrated glomerular damage with a decrease in urinary creatinine. Our results prove that tau has an important role in kidney metabolism under normal physiological conditions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00018-021-04106-z. |
format | Online Article Text |
id | pubmed-8794918 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-87949182022-02-02 Microtubule-associated protein tau in murine kidney: role in podocyte architecture Vallés-Saiz, Laura Peinado-Cahuchola, Rocio Ávila, Jesús Hernández, Félix Cell Mol Life Sci Original Article Tau is a cytoskeletal protein that is expressed mainly in neurons and is involved in several cellular processes, such as microtubule stabilization, axonal maintenance, and transport. Altered tau metabolism is related to different tauopathies being the most important Alzheimer’s disease where aberrant hyperphosphorylated and aggregated tau is found in the central nervous system. Here, we have analyzed that function in kidney by using tau knockout mice generated by integrating GFP-encoding cDNA into exon 1 of MAPT (here referred to as Tau(GFP/GFP)). IVIS Lumina from PerkinElmer demonstrated GFP expression in the kidney. We then demonstrated by qPCR that the main tau isoform in the kidney is Tau4R. The GFP reporter allowed us to demonstrate that tau is found in the glomeruli of the renal cortex, and specifically in podocytes. This was further confirmed by immunohistochemistry. Tau(GFP/GFP) mice present a podocyte cytoskeleton more dynamic as they contain higher levels of detyrosinated tubulin than wild-type mice. In addition, transmission electron microscopy studies demonstrated glomerular damage with a decrease in urinary creatinine. Our results prove that tau has an important role in kidney metabolism under normal physiological conditions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00018-021-04106-z. Springer International Publishing 2022-01-27 2022 /pmc/articles/PMC8794918/ /pubmed/35084555 http://dx.doi.org/10.1007/s00018-021-04106-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Vallés-Saiz, Laura Peinado-Cahuchola, Rocio Ávila, Jesús Hernández, Félix Microtubule-associated protein tau in murine kidney: role in podocyte architecture |
title | Microtubule-associated protein tau in murine kidney: role in podocyte architecture |
title_full | Microtubule-associated protein tau in murine kidney: role in podocyte architecture |
title_fullStr | Microtubule-associated protein tau in murine kidney: role in podocyte architecture |
title_full_unstemmed | Microtubule-associated protein tau in murine kidney: role in podocyte architecture |
title_short | Microtubule-associated protein tau in murine kidney: role in podocyte architecture |
title_sort | microtubule-associated protein tau in murine kidney: role in podocyte architecture |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8794918/ https://www.ncbi.nlm.nih.gov/pubmed/35084555 http://dx.doi.org/10.1007/s00018-021-04106-z |
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