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Glycolysis, but not Mitochondria, responsible for intracellular ATP distribution in cortical area of podocytes

Differentiated podocytes, a type of renal glomerular cells, require substantial levels of energy to maintain glomerular physiology. Mitochondria and glycolysis are two major producers of ATP, but the precise roles of each in podocytes remain unknown. This study evaluated the roles of mitochondria an...

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Autores principales: Ozawa, Shota, Ueda, Shuko, Imamura, Hiromi, Mori, Kiyoshi, Asanuma, Katsuhiko, Yanagita, Motoko, Nakagawa, Takahiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4683464/
https://www.ncbi.nlm.nih.gov/pubmed/26677804
http://dx.doi.org/10.1038/srep18575
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author Ozawa, Shota
Ueda, Shuko
Imamura, Hiromi
Mori, Kiyoshi
Asanuma, Katsuhiko
Yanagita, Motoko
Nakagawa, Takahiko
author_facet Ozawa, Shota
Ueda, Shuko
Imamura, Hiromi
Mori, Kiyoshi
Asanuma, Katsuhiko
Yanagita, Motoko
Nakagawa, Takahiko
author_sort Ozawa, Shota
collection PubMed
description Differentiated podocytes, a type of renal glomerular cells, require substantial levels of energy to maintain glomerular physiology. Mitochondria and glycolysis are two major producers of ATP, but the precise roles of each in podocytes remain unknown. This study evaluated the roles of mitochondria and glycolysis in differentiated and differentiating podocytes. Mitochondria in differentiated podocytes are located in the central part of cell body while blocking mitochondria had minor effects on cell shape and migratory ability. In contrast, blocking glycolysis significantly reduced the formation of lamellipodia, a cortical area of these cells, decreased the cell migratory ability and induced the apoptosis. Consistently, the local ATP production in lamellipodia was predominantly regulated by glycolysis. In turn, synaptopodin expression was ameliorated by blocking either mitochondrial respiration or glycolysis. Similar to differentiated podocytes, the differentiating podocytes utilized the glycolysis for regulating apoptosis and lamellipodia formation while synaptopodin expression was likely involved in both mitochondrial OXPHOS and glycolysis. Finally, adult mouse podocytes have most of mitochondria predominantly in the center of the cytosol whereas phosphofructokinase, a rate limiting enzyme for glycolysis, was expressed in foot processes. These data suggest that mitochondria and glycolysis play parallel but distinct roles in differentiated and differentiating podocytes.
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spelling pubmed-46834642015-12-21 Glycolysis, but not Mitochondria, responsible for intracellular ATP distribution in cortical area of podocytes Ozawa, Shota Ueda, Shuko Imamura, Hiromi Mori, Kiyoshi Asanuma, Katsuhiko Yanagita, Motoko Nakagawa, Takahiko Sci Rep Article Differentiated podocytes, a type of renal glomerular cells, require substantial levels of energy to maintain glomerular physiology. Mitochondria and glycolysis are two major producers of ATP, but the precise roles of each in podocytes remain unknown. This study evaluated the roles of mitochondria and glycolysis in differentiated and differentiating podocytes. Mitochondria in differentiated podocytes are located in the central part of cell body while blocking mitochondria had minor effects on cell shape and migratory ability. In contrast, blocking glycolysis significantly reduced the formation of lamellipodia, a cortical area of these cells, decreased the cell migratory ability and induced the apoptosis. Consistently, the local ATP production in lamellipodia was predominantly regulated by glycolysis. In turn, synaptopodin expression was ameliorated by blocking either mitochondrial respiration or glycolysis. Similar to differentiated podocytes, the differentiating podocytes utilized the glycolysis for regulating apoptosis and lamellipodia formation while synaptopodin expression was likely involved in both mitochondrial OXPHOS and glycolysis. Finally, adult mouse podocytes have most of mitochondria predominantly in the center of the cytosol whereas phosphofructokinase, a rate limiting enzyme for glycolysis, was expressed in foot processes. These data suggest that mitochondria and glycolysis play parallel but distinct roles in differentiated and differentiating podocytes. Nature Publishing Group 2015-12-18 /pmc/articles/PMC4683464/ /pubmed/26677804 http://dx.doi.org/10.1038/srep18575 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Ozawa, Shota
Ueda, Shuko
Imamura, Hiromi
Mori, Kiyoshi
Asanuma, Katsuhiko
Yanagita, Motoko
Nakagawa, Takahiko
Glycolysis, but not Mitochondria, responsible for intracellular ATP distribution in cortical area of podocytes
title Glycolysis, but not Mitochondria, responsible for intracellular ATP distribution in cortical area of podocytes
title_full Glycolysis, but not Mitochondria, responsible for intracellular ATP distribution in cortical area of podocytes
title_fullStr Glycolysis, but not Mitochondria, responsible for intracellular ATP distribution in cortical area of podocytes
title_full_unstemmed Glycolysis, but not Mitochondria, responsible for intracellular ATP distribution in cortical area of podocytes
title_short Glycolysis, but not Mitochondria, responsible for intracellular ATP distribution in cortical area of podocytes
title_sort glycolysis, but not mitochondria, responsible for intracellular atp distribution in cortical area of podocytes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4683464/
https://www.ncbi.nlm.nih.gov/pubmed/26677804
http://dx.doi.org/10.1038/srep18575
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