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Reducing l‐lactate release from hippocampal astrocytes by intracellular oxidation increases novelty induced activity in mice

Astrocytes are in control of metabolic homeostasis in the brain and support and modulate neuronal function in various ways. Astrocyte‐derived l‐lactate (lactate) is thought to play a dual role as a metabolic and a signaling molecule in inter‐cellular communication. The biological significance of lac...

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Autores principales: Vaccari Cardoso, Barbara, Shevelkin, Alexey V., Terrillion, Chantelle, Mychko, Olga, Mosienko, Valentina, Kasparov, Sergey, Pletnikov, Mikhail V., Teschemacher, Anja G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8576740/
https://www.ncbi.nlm.nih.gov/pubmed/33400321
http://dx.doi.org/10.1002/glia.23960
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author Vaccari Cardoso, Barbara
Shevelkin, Alexey V.
Terrillion, Chantelle
Mychko, Olga
Mosienko, Valentina
Kasparov, Sergey
Pletnikov, Mikhail V.
Teschemacher, Anja G.
author_facet Vaccari Cardoso, Barbara
Shevelkin, Alexey V.
Terrillion, Chantelle
Mychko, Olga
Mosienko, Valentina
Kasparov, Sergey
Pletnikov, Mikhail V.
Teschemacher, Anja G.
author_sort Vaccari Cardoso, Barbara
collection PubMed
description Astrocytes are in control of metabolic homeostasis in the brain and support and modulate neuronal function in various ways. Astrocyte‐derived l‐lactate (lactate) is thought to play a dual role as a metabolic and a signaling molecule in inter‐cellular communication. The biological significance of lactate release from astrocytes is poorly understood, largely because the tools to manipulate lactate levels in vivo are limited. We therefore developed new viral vectors for astrocyte‐specific expression of a mammalianized version of lactate oxidase (LOx) from Aerococcus viridans. LOx expression in astrocytes in vitro reduced their intracellular lactate levels as well as the release of lactate to the extracellular space. Selective expression of LOx in astrocytes of the dorsal hippocampus in mice resulted in increased locomotor activity in response to novel stimuli. Our findings suggest that a localized decreased intracellular lactate pool in hippocampal astrocytes could contribute to greater responsiveness to environmental novelty. We expect that use of this molecular tool to chronically limit astrocytic lactate release will significantly facilitate future studies into the roles and mechanisms of intercellular lactate communication in the brain.
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spelling pubmed-85767402021-11-15 Reducing l‐lactate release from hippocampal astrocytes by intracellular oxidation increases novelty induced activity in mice Vaccari Cardoso, Barbara Shevelkin, Alexey V. Terrillion, Chantelle Mychko, Olga Mosienko, Valentina Kasparov, Sergey Pletnikov, Mikhail V. Teschemacher, Anja G. Glia Research Articles Astrocytes are in control of metabolic homeostasis in the brain and support and modulate neuronal function in various ways. Astrocyte‐derived l‐lactate (lactate) is thought to play a dual role as a metabolic and a signaling molecule in inter‐cellular communication. The biological significance of lactate release from astrocytes is poorly understood, largely because the tools to manipulate lactate levels in vivo are limited. We therefore developed new viral vectors for astrocyte‐specific expression of a mammalianized version of lactate oxidase (LOx) from Aerococcus viridans. LOx expression in astrocytes in vitro reduced their intracellular lactate levels as well as the release of lactate to the extracellular space. Selective expression of LOx in astrocytes of the dorsal hippocampus in mice resulted in increased locomotor activity in response to novel stimuli. Our findings suggest that a localized decreased intracellular lactate pool in hippocampal astrocytes could contribute to greater responsiveness to environmental novelty. We expect that use of this molecular tool to chronically limit astrocytic lactate release will significantly facilitate future studies into the roles and mechanisms of intercellular lactate communication in the brain. John Wiley & Sons, Inc. 2021-01-05 2021-05 /pmc/articles/PMC8576740/ /pubmed/33400321 http://dx.doi.org/10.1002/glia.23960 Text en © 2021 The Authors. Glia published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Vaccari Cardoso, Barbara
Shevelkin, Alexey V.
Terrillion, Chantelle
Mychko, Olga
Mosienko, Valentina
Kasparov, Sergey
Pletnikov, Mikhail V.
Teschemacher, Anja G.
Reducing l‐lactate release from hippocampal astrocytes by intracellular oxidation increases novelty induced activity in mice
title Reducing l‐lactate release from hippocampal astrocytes by intracellular oxidation increases novelty induced activity in mice
title_full Reducing l‐lactate release from hippocampal astrocytes by intracellular oxidation increases novelty induced activity in mice
title_fullStr Reducing l‐lactate release from hippocampal astrocytes by intracellular oxidation increases novelty induced activity in mice
title_full_unstemmed Reducing l‐lactate release from hippocampal astrocytes by intracellular oxidation increases novelty induced activity in mice
title_short Reducing l‐lactate release from hippocampal astrocytes by intracellular oxidation increases novelty induced activity in mice
title_sort reducing l‐lactate release from hippocampal astrocytes by intracellular oxidation increases novelty induced activity in mice
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8576740/
https://www.ncbi.nlm.nih.gov/pubmed/33400321
http://dx.doi.org/10.1002/glia.23960
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