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Local and dynamic regulation of neuronal glycolysis in vivo

Energy metabolism supports neuronal function. While it is well established that changes in energy metabolism underpin brain plasticity and function, less is known about how individual neurons modulate their metabolic states to meet varying energy demands. This is because most approaches used to exam...

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Autores principales: Wolfe, Aaron D., Koberstein, John N, Smith, Chadwick B, Stewart, Melissa L, Hammarlund, Marc, Hyman, Anthony, Stork, Philip JS, Goodman, Richard, Colón-Ramos, Daniel A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10473759/
https://www.ncbi.nlm.nih.gov/pubmed/37662365
http://dx.doi.org/10.1101/2023.08.25.554774
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author Wolfe, Aaron D.
Koberstein, John N
Smith, Chadwick B
Stewart, Melissa L
Hammarlund, Marc
Hyman, Anthony
Stork, Philip JS
Goodman, Richard
Colón-Ramos, Daniel A.
author_facet Wolfe, Aaron D.
Koberstein, John N
Smith, Chadwick B
Stewart, Melissa L
Hammarlund, Marc
Hyman, Anthony
Stork, Philip JS
Goodman, Richard
Colón-Ramos, Daniel A.
author_sort Wolfe, Aaron D.
collection PubMed
description Energy metabolism supports neuronal function. While it is well established that changes in energy metabolism underpin brain plasticity and function, less is known about how individual neurons modulate their metabolic states to meet varying energy demands. This is because most approaches used to examine metabolism in living organisms lack the resolution to visualize energy metabolism within individual circuits, cells, or subcellular regions. Here we adapted a biosensor for glycolysis, HYlight, for use in C. elegans to image dynamic changes in glycolysis within individual neurons and in vivo. We determined that neurons perform glycolysis cell-autonomously, and modulate glycolytic states upon energy stress. By examining glycolysis in specific neurons, we documented a neuronal energy landscape comprising three general observations: 1) glycolytic states in neurons are diverse across individual cell types; 2) for a given condition, glycolytic states within individual neurons are reproducible across animals; and 3) for varying conditions of energy stress, glycolytic states are plastic and adapt to energy demands. Through genetic analyses, we uncovered roles for regulatory enzymes and mitochondrial localization in the cellular and subcellular dynamic regulation of glycolysis. Our study demonstrates the use of a single-cell glycolytic biosensor to examine how energy metabolism is distributed across cells and coupled to dynamic states of neuronal function, and uncovers new relationships between neuronal identities and metabolic landscapes in vivo.
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spelling pubmed-104737592023-09-02 Local and dynamic regulation of neuronal glycolysis in vivo Wolfe, Aaron D. Koberstein, John N Smith, Chadwick B Stewart, Melissa L Hammarlund, Marc Hyman, Anthony Stork, Philip JS Goodman, Richard Colón-Ramos, Daniel A. bioRxiv Article Energy metabolism supports neuronal function. While it is well established that changes in energy metabolism underpin brain plasticity and function, less is known about how individual neurons modulate their metabolic states to meet varying energy demands. This is because most approaches used to examine metabolism in living organisms lack the resolution to visualize energy metabolism within individual circuits, cells, or subcellular regions. Here we adapted a biosensor for glycolysis, HYlight, for use in C. elegans to image dynamic changes in glycolysis within individual neurons and in vivo. We determined that neurons perform glycolysis cell-autonomously, and modulate glycolytic states upon energy stress. By examining glycolysis in specific neurons, we documented a neuronal energy landscape comprising three general observations: 1) glycolytic states in neurons are diverse across individual cell types; 2) for a given condition, glycolytic states within individual neurons are reproducible across animals; and 3) for varying conditions of energy stress, glycolytic states are plastic and adapt to energy demands. Through genetic analyses, we uncovered roles for regulatory enzymes and mitochondrial localization in the cellular and subcellular dynamic regulation of glycolysis. Our study demonstrates the use of a single-cell glycolytic biosensor to examine how energy metabolism is distributed across cells and coupled to dynamic states of neuronal function, and uncovers new relationships between neuronal identities and metabolic landscapes in vivo. Cold Spring Harbor Laboratory 2023-08-26 /pmc/articles/PMC10473759/ /pubmed/37662365 http://dx.doi.org/10.1101/2023.08.25.554774 Text en https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Wolfe, Aaron D.
Koberstein, John N
Smith, Chadwick B
Stewart, Melissa L
Hammarlund, Marc
Hyman, Anthony
Stork, Philip JS
Goodman, Richard
Colón-Ramos, Daniel A.
Local and dynamic regulation of neuronal glycolysis in vivo
title Local and dynamic regulation of neuronal glycolysis in vivo
title_full Local and dynamic regulation of neuronal glycolysis in vivo
title_fullStr Local and dynamic regulation of neuronal glycolysis in vivo
title_full_unstemmed Local and dynamic regulation of neuronal glycolysis in vivo
title_short Local and dynamic regulation of neuronal glycolysis in vivo
title_sort local and dynamic regulation of neuronal glycolysis in vivo
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10473759/
https://www.ncbi.nlm.nih.gov/pubmed/37662365
http://dx.doi.org/10.1101/2023.08.25.554774
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