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Erythropoietin promotes hippocampal mitochondrial function and enhances cognition in mice
Erythropoietin (EPO) improves neuronal mitochondrial function and cognition in adults after brain injury and in those afflicted by psychiatric disorders. However, the influence of EPO on mitochondria and cognition during development remains unexplored. We previously observed that EPO stimulates hipp...
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/PMC8342552/ https://www.ncbi.nlm.nih.gov/pubmed/34354241 http://dx.doi.org/10.1038/s42003-021-02465-8 |
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author | Jacobs, Robert A. Aboouf, Mostafa A. Koester-Hegmann, Christina Muttathukunnel, Paola Laouafa, Sofien Arias-Reyes, Christian Thiersch, Markus Soliz, Jorge Gassmann, Max Schneider Gasser, Edith M. |
author_facet | Jacobs, Robert A. Aboouf, Mostafa A. Koester-Hegmann, Christina Muttathukunnel, Paola Laouafa, Sofien Arias-Reyes, Christian Thiersch, Markus Soliz, Jorge Gassmann, Max Schneider Gasser, Edith M. |
author_sort | Jacobs, Robert A. |
collection | PubMed |
description | Erythropoietin (EPO) improves neuronal mitochondrial function and cognition in adults after brain injury and in those afflicted by psychiatric disorders. However, the influence of EPO on mitochondria and cognition during development remains unexplored. We previously observed that EPO stimulates hippocampal-specific neuronal maturation and synaptogenesis early in postnatal development in mice. Here we show that EPO promotes mitochondrial respiration in developing postnatal hippocampus by increasing mitochondrial content and enhancing cellular respiratory potential. Ultrastructurally, mitochondria profiles and total vesicle content were greater in presynaptic axon terminals, suggesting that EPO enhances oxidative metabolism and synaptic transmission capabilities. Behavioural tests of hippocampus-dependent memory at early adulthood, showed that EPO improves spatial and short-term memory. Collectively, we identify a role for EPO in the murine postnatal hippocampus by promoting mitochondrial function throughout early postnatal development, which corresponds to enhanced cognition by early adulthood. |
format | Online Article Text |
id | pubmed-8342552 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-83425522021-08-20 Erythropoietin promotes hippocampal mitochondrial function and enhances cognition in mice Jacobs, Robert A. Aboouf, Mostafa A. Koester-Hegmann, Christina Muttathukunnel, Paola Laouafa, Sofien Arias-Reyes, Christian Thiersch, Markus Soliz, Jorge Gassmann, Max Schneider Gasser, Edith M. Commun Biol Article Erythropoietin (EPO) improves neuronal mitochondrial function and cognition in adults after brain injury and in those afflicted by psychiatric disorders. However, the influence of EPO on mitochondria and cognition during development remains unexplored. We previously observed that EPO stimulates hippocampal-specific neuronal maturation and synaptogenesis early in postnatal development in mice. Here we show that EPO promotes mitochondrial respiration in developing postnatal hippocampus by increasing mitochondrial content and enhancing cellular respiratory potential. Ultrastructurally, mitochondria profiles and total vesicle content were greater in presynaptic axon terminals, suggesting that EPO enhances oxidative metabolism and synaptic transmission capabilities. Behavioural tests of hippocampus-dependent memory at early adulthood, showed that EPO improves spatial and short-term memory. Collectively, we identify a role for EPO in the murine postnatal hippocampus by promoting mitochondrial function throughout early postnatal development, which corresponds to enhanced cognition by early adulthood. Nature Publishing Group UK 2021-08-05 /pmc/articles/PMC8342552/ /pubmed/34354241 http://dx.doi.org/10.1038/s42003-021-02465-8 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 Jacobs, Robert A. Aboouf, Mostafa A. Koester-Hegmann, Christina Muttathukunnel, Paola Laouafa, Sofien Arias-Reyes, Christian Thiersch, Markus Soliz, Jorge Gassmann, Max Schneider Gasser, Edith M. Erythropoietin promotes hippocampal mitochondrial function and enhances cognition in mice |
title | Erythropoietin promotes hippocampal mitochondrial function and enhances cognition in mice |
title_full | Erythropoietin promotes hippocampal mitochondrial function and enhances cognition in mice |
title_fullStr | Erythropoietin promotes hippocampal mitochondrial function and enhances cognition in mice |
title_full_unstemmed | Erythropoietin promotes hippocampal mitochondrial function and enhances cognition in mice |
title_short | Erythropoietin promotes hippocampal mitochondrial function and enhances cognition in mice |
title_sort | erythropoietin promotes hippocampal mitochondrial function and enhances cognition in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8342552/ https://www.ncbi.nlm.nih.gov/pubmed/34354241 http://dx.doi.org/10.1038/s42003-021-02465-8 |
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