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Acetoacetate protects macrophages from lactic acidosis-induced mitochondrial dysfunction by metabolic reprograming
Lactic acidosis, the extracellular accumulation of lactate and protons, is a consequence of increased glycolysis triggered by insufficient oxygen supply to tissues. Macrophages are able to differentiate from monocytes under such acidotic conditions, and remain active in order to resolve the underlyi...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8655019/ https://www.ncbi.nlm.nih.gov/pubmed/34880237 http://dx.doi.org/10.1038/s41467-021-27426-x |
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author | Adam, Clément Paolini, Léa Gueguen, Naïg Mabilleau, Guillaume Preisser, Laurence Blanchard, Simon Pignon, Pascale Manero, Florence Le Mao, Morgane Morel, Alain Reynier, Pascal Beauvillain, Céline Delneste, Yves Procaccio, Vincent Jeannin, Pascale |
author_facet | Adam, Clément Paolini, Léa Gueguen, Naïg Mabilleau, Guillaume Preisser, Laurence Blanchard, Simon Pignon, Pascale Manero, Florence Le Mao, Morgane Morel, Alain Reynier, Pascal Beauvillain, Céline Delneste, Yves Procaccio, Vincent Jeannin, Pascale |
author_sort | Adam, Clément |
collection | PubMed |
description | Lactic acidosis, the extracellular accumulation of lactate and protons, is a consequence of increased glycolysis triggered by insufficient oxygen supply to tissues. Macrophages are able to differentiate from monocytes under such acidotic conditions, and remain active in order to resolve the underlying injury. Here we show that, in lactic acidosis, human monocytes differentiating into macrophages are characterized by depolarized mitochondria, transient reduction of mitochondrial mass due to mitophagy, and a significant decrease in nutrient absorption. These metabolic changes, resembling pseudostarvation, result from the low extracellular pH rather than from the lactosis component, and render these cells dependent on autophagy for survival. Meanwhile, acetoacetate, a natural metabolite produced by the liver, is utilized by monocytes/macrophages as an alternative fuel to mitigate lactic acidosis-induced pseudostarvation, as evidenced by retained mitochondrial integrity and function, retained nutrient uptake, and survival without the need of autophagy. Our results thus show that acetoacetate may increase tissue tolerance to sustained lactic acidosis. |
format | Online Article Text |
id | pubmed-8655019 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-86550192021-12-27 Acetoacetate protects macrophages from lactic acidosis-induced mitochondrial dysfunction by metabolic reprograming Adam, Clément Paolini, Léa Gueguen, Naïg Mabilleau, Guillaume Preisser, Laurence Blanchard, Simon Pignon, Pascale Manero, Florence Le Mao, Morgane Morel, Alain Reynier, Pascal Beauvillain, Céline Delneste, Yves Procaccio, Vincent Jeannin, Pascale Nat Commun Article Lactic acidosis, the extracellular accumulation of lactate and protons, is a consequence of increased glycolysis triggered by insufficient oxygen supply to tissues. Macrophages are able to differentiate from monocytes under such acidotic conditions, and remain active in order to resolve the underlying injury. Here we show that, in lactic acidosis, human monocytes differentiating into macrophages are characterized by depolarized mitochondria, transient reduction of mitochondrial mass due to mitophagy, and a significant decrease in nutrient absorption. These metabolic changes, resembling pseudostarvation, result from the low extracellular pH rather than from the lactosis component, and render these cells dependent on autophagy for survival. Meanwhile, acetoacetate, a natural metabolite produced by the liver, is utilized by monocytes/macrophages as an alternative fuel to mitigate lactic acidosis-induced pseudostarvation, as evidenced by retained mitochondrial integrity and function, retained nutrient uptake, and survival without the need of autophagy. Our results thus show that acetoacetate may increase tissue tolerance to sustained lactic acidosis. Nature Publishing Group UK 2021-12-08 /pmc/articles/PMC8655019/ /pubmed/34880237 http://dx.doi.org/10.1038/s41467-021-27426-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Adam, Clément Paolini, Léa Gueguen, Naïg Mabilleau, Guillaume Preisser, Laurence Blanchard, Simon Pignon, Pascale Manero, Florence Le Mao, Morgane Morel, Alain Reynier, Pascal Beauvillain, Céline Delneste, Yves Procaccio, Vincent Jeannin, Pascale Acetoacetate protects macrophages from lactic acidosis-induced mitochondrial dysfunction by metabolic reprograming |
title | Acetoacetate protects macrophages from lactic acidosis-induced mitochondrial dysfunction by metabolic reprograming |
title_full | Acetoacetate protects macrophages from lactic acidosis-induced mitochondrial dysfunction by metabolic reprograming |
title_fullStr | Acetoacetate protects macrophages from lactic acidosis-induced mitochondrial dysfunction by metabolic reprograming |
title_full_unstemmed | Acetoacetate protects macrophages from lactic acidosis-induced mitochondrial dysfunction by metabolic reprograming |
title_short | Acetoacetate protects macrophages from lactic acidosis-induced mitochondrial dysfunction by metabolic reprograming |
title_sort | acetoacetate protects macrophages from lactic acidosis-induced mitochondrial dysfunction by metabolic reprograming |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8655019/ https://www.ncbi.nlm.nih.gov/pubmed/34880237 http://dx.doi.org/10.1038/s41467-021-27426-x |
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