Distinct reduction in relative microglial glucose uptake compared to astrocytes and neurons upon isolation from the brain environment

IntroductionMicroglial energy metabolism has gained attention for the treatment of neurodegenerative diseases. In vitro methods provide important insights; however, it remains unclear whether the metabolism of highly motile microglia is preserved outside their regular environment. Therefore, we dire...

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Published in:Frontiers in Cellular Neuroscience
Main Authors: Sebastian T. Kunte, Johannes Gnörich, Philipp Beumers, Laura M. Bartos, Stephan Wagner, Karin Wind-Mark, Adrien Holzgreve, Dennis Pötter, Rudolf A. Werner, Sibylle Ziegler, Nathalie L. Albert, Alessio Colombo, Sabina Tahirovic, Matthias Brendel
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Language:English
Published: Frontiers Media S.A. 2025-09-01
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Online Access:https://www.frontiersin.org/articles/10.3389/fncel.2025.1572431/full
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author Sebastian T. Kunte
Sebastian T. Kunte
Johannes Gnörich
Johannes Gnörich
Philipp Beumers
Laura M. Bartos
Stephan Wagner
Karin Wind-Mark
Adrien Holzgreve
Dennis Pötter
Rudolf A. Werner
Rudolf A. Werner
Sibylle Ziegler
Sibylle Ziegler
Nathalie L. Albert
Nathalie L. Albert
Nathalie L. Albert
Alessio Colombo
Sabina Tahirovic
Matthias Brendel
Matthias Brendel
Matthias Brendel
Matthias Brendel
Matthias Brendel
author_facet Sebastian T. Kunte
Sebastian T. Kunte
Johannes Gnörich
Johannes Gnörich
Philipp Beumers
Laura M. Bartos
Stephan Wagner
Karin Wind-Mark
Adrien Holzgreve
Dennis Pötter
Rudolf A. Werner
Rudolf A. Werner
Sibylle Ziegler
Sibylle Ziegler
Nathalie L. Albert
Nathalie L. Albert
Nathalie L. Albert
Alessio Colombo
Sabina Tahirovic
Matthias Brendel
Matthias Brendel
Matthias Brendel
Matthias Brendel
Matthias Brendel
author_sort Sebastian T. Kunte
collection DOAJ
container_title Frontiers in Cellular Neuroscience
description IntroductionMicroglial energy metabolism has gained attention for the treatment of neurodegenerative diseases. In vitro methods provide important insights; however, it remains unclear whether the metabolism of highly motile microglia is preserved outside their regular environment. Therefore, we directly compared the microglial glucose uptake in vivo and in vitro in mice.MethodsMicroglia and astrocytes were isolated from the brain using immunomagnetic cell sorting following [18F]FDG injection in living mice, followed by gamma and single-cell radiotracing (scRadiotracing). Enriched cell fractions were incubated with excess [18F]FDG (50,000-fold) in vivo, washed, and measured equivalently. For all fractions, radioactivity per cell was normalized to the injected or incubated radioactivity, and ratios of microglialuptake were calculated relative to astrocytes and the microglia/astrocyte-negative fraction. The experiment was repeated using a glucose-free buffer and validated by in vitro incubation without prior in vivo [18F]FDG injection to exclude the influence of fasting and glucose injection.ResultsscRadiotracing results were compared against cell culture [18F]-FDG incubation. The in vivo glucose uptake of microglia was higher when compared to astrocytes (50.4-fold, p < 0.0001) and non-microglia/ non-astrocyte cells (10.6-fold, p < 0.0001). Microglia still exhibited the highest glucose uptake in vitro, but with a distinct reduction in microglia-to-astrocyte (5.7-fold, p < 0.0015) and microglia-to-microglia/astrocyte-negative ratios (1.7 fold, p < 0.0001). Fasting and in vitro incubation were used to validate the results. Cell culture indicated low microglial uptake compared to that in neurons (1:100) or astrocytes (1:10).DiscussionCompared to astrocytes and other cells, microglia show a distinct reduction in uptake in vitro compared to in vivo uptake. Our results emphasize that in vitro experiments should be interpreted with caution when studying microglial energy metabolism.
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spelling doaj-art-07762d0dcafe4751a2e1056d92f4961c2025-09-15T05:32:13ZengFrontiers Media S.A.Frontiers in Cellular Neuroscience1662-51022025-09-011910.3389/fncel.2025.15724311572431Distinct reduction in relative microglial glucose uptake compared to astrocytes and neurons upon isolation from the brain environmentSebastian T. Kunte0Sebastian T. Kunte1Johannes Gnörich2Johannes Gnörich3Philipp Beumers4Laura M. Bartos5Stephan Wagner6Karin Wind-Mark7Adrien Holzgreve8Dennis Pötter9Rudolf A. Werner10Rudolf A. Werner11Sibylle Ziegler12Sibylle Ziegler13Nathalie L. Albert14Nathalie L. Albert15Nathalie L. Albert16Alessio Colombo17Sabina Tahirovic18Matthias Brendel19Matthias Brendel20Matthias Brendel21Matthias Brendel22Matthias Brendel23Department of Nuclear Medicine, LMU University Hospital, Munich, GermanySection of Clinical and Comparative Neuropathology, Institute for Veterinary Pathology, Center for Clinical Veterinary Medicine, LMU, Munich, GermanyDepartment of Nuclear Medicine, LMU University Hospital, Munich, GermanyMunich Cluster for Systems Neurology (SyNergy), University of Munich, Munich, GermanyDepartment of Nuclear Medicine, LMU University Hospital, Munich, GermanyDepartment of Nuclear Medicine, LMU University Hospital, Munich, GermanyDepartment of Nuclear Medicine, LMU University Hospital, Munich, GermanyDepartment of Nuclear Medicine, LMU University Hospital, Munich, GermanyDepartment of Nuclear Medicine, LMU University Hospital, Munich, GermanyDepartment of Nuclear Medicine, LMU University Hospital, Munich, GermanyDepartment of Nuclear Medicine, LMU University Hospital, Munich, GermanyRussell H. Morgan Department of Radiology and Radiological Sciences, Johns Hopkins School of Medicine, Baltimore, MD, United StatesDepartment of Nuclear Medicine, LMU University Hospital, Munich, GermanyMunich Cluster for Systems Neurology (SyNergy), University of Munich, Munich, GermanyDepartment of Nuclear Medicine, LMU University Hospital, Munich, GermanyGerman Cancer Consortium (DKTK), Partner Site Munich, German Cancer Research Center (DKFZ), Heidelberg, GermanyBavarian Cancer Research Center (BZKF), Erlangen, GermanyGerman Center for Neurodegenerative Diseases (DZNE) Munich, Munich, GermanyGerman Center for Neurodegenerative Diseases (DZNE) Munich, Munich, GermanyDepartment of Nuclear Medicine, LMU University Hospital, Munich, GermanyMunich Cluster for Systems Neurology (SyNergy), University of Munich, Munich, GermanyGerman Cancer Consortium (DKTK), Partner Site Munich, German Cancer Research Center (DKFZ), Heidelberg, GermanyBavarian Cancer Research Center (BZKF), Erlangen, GermanyGerman Center for Neurodegenerative Diseases (DZNE) Munich, Munich, GermanyIntroductionMicroglial energy metabolism has gained attention for the treatment of neurodegenerative diseases. In vitro methods provide important insights; however, it remains unclear whether the metabolism of highly motile microglia is preserved outside their regular environment. Therefore, we directly compared the microglial glucose uptake in vivo and in vitro in mice.MethodsMicroglia and astrocytes were isolated from the brain using immunomagnetic cell sorting following [18F]FDG injection in living mice, followed by gamma and single-cell radiotracing (scRadiotracing). Enriched cell fractions were incubated with excess [18F]FDG (50,000-fold) in vivo, washed, and measured equivalently. For all fractions, radioactivity per cell was normalized to the injected or incubated radioactivity, and ratios of microglialuptake were calculated relative to astrocytes and the microglia/astrocyte-negative fraction. The experiment was repeated using a glucose-free buffer and validated by in vitro incubation without prior in vivo [18F]FDG injection to exclude the influence of fasting and glucose injection.ResultsscRadiotracing results were compared against cell culture [18F]-FDG incubation. The in vivo glucose uptake of microglia was higher when compared to astrocytes (50.4-fold, p < 0.0001) and non-microglia/ non-astrocyte cells (10.6-fold, p < 0.0001). Microglia still exhibited the highest glucose uptake in vitro, but with a distinct reduction in microglia-to-astrocyte (5.7-fold, p < 0.0015) and microglia-to-microglia/astrocyte-negative ratios (1.7 fold, p < 0.0001). Fasting and in vitro incubation were used to validate the results. Cell culture indicated low microglial uptake compared to that in neurons (1:100) or astrocytes (1:10).DiscussionCompared to astrocytes and other cells, microglia show a distinct reduction in uptake in vitro compared to in vivo uptake. Our results emphasize that in vitro experiments should be interpreted with caution when studying microglial energy metabolism.https://www.frontiersin.org/articles/10.3389/fncel.2025.1572431/fullmicrogliaglucose uptakein vivoin vitroscRadiotracing
spellingShingle Sebastian T. Kunte
Sebastian T. Kunte
Johannes Gnörich
Johannes Gnörich
Philipp Beumers
Laura M. Bartos
Stephan Wagner
Karin Wind-Mark
Adrien Holzgreve
Dennis Pötter
Rudolf A. Werner
Rudolf A. Werner
Sibylle Ziegler
Sibylle Ziegler
Nathalie L. Albert
Nathalie L. Albert
Nathalie L. Albert
Alessio Colombo
Sabina Tahirovic
Matthias Brendel
Matthias Brendel
Matthias Brendel
Matthias Brendel
Matthias Brendel
Distinct reduction in relative microglial glucose uptake compared to astrocytes and neurons upon isolation from the brain environment
microglia
glucose uptake
in vivo
in vitro
scRadiotracing
title Distinct reduction in relative microglial glucose uptake compared to astrocytes and neurons upon isolation from the brain environment
title_full Distinct reduction in relative microglial glucose uptake compared to astrocytes and neurons upon isolation from the brain environment
title_fullStr Distinct reduction in relative microglial glucose uptake compared to astrocytes and neurons upon isolation from the brain environment
title_full_unstemmed Distinct reduction in relative microglial glucose uptake compared to astrocytes and neurons upon isolation from the brain environment
title_short Distinct reduction in relative microglial glucose uptake compared to astrocytes and neurons upon isolation from the brain environment
title_sort distinct reduction in relative microglial glucose uptake compared to astrocytes and neurons upon isolation from the brain environment
topic microglia
glucose uptake
in vivo
in vitro
scRadiotracing
url https://www.frontiersin.org/articles/10.3389/fncel.2025.1572431/full
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