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Characterization of glucose‐related metabolic pathways in differentiated rat oligodendrocyte lineage cells
Although oligodendrocytes constitute a significant proportion of cells in the central nervous system (CNS), little is known about their intermediary metabolism. We have, therefore, characterized metabolic functions of primary oligodendrocyte precursor cell cultures at late stages of differentiation...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4832329/ https://www.ncbi.nlm.nih.gov/pubmed/26352325 http://dx.doi.org/10.1002/glia.22900 |
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author | Amaral, Ana I. Hadera, Mussie G. Tavares, Joana M. Kotter, Mark R. N. Sonnewald, Ursula |
author_facet | Amaral, Ana I. Hadera, Mussie G. Tavares, Joana M. Kotter, Mark R. N. Sonnewald, Ursula |
author_sort | Amaral, Ana I. |
collection | PubMed |
description | Although oligodendrocytes constitute a significant proportion of cells in the central nervous system (CNS), little is known about their intermediary metabolism. We have, therefore, characterized metabolic functions of primary oligodendrocyte precursor cell cultures at late stages of differentiation using isotope‐labelled metabolites. We report that differentiated oligodendrocyte lineage cells avidly metabolize glucose in the cytosol and pyruvate derived from glucose in the mitochondria. The labelling patterns of metabolites obtained after incubation with [1,2‐(13)C]glucose demonstrated that the pentose phosphate pathway (PPP) is highly active in oligodendrocytes (approximately 10% of glucose is metabolized via the PPP as indicated by labelling patterns in phosphoenolpyruvate). Mass spectrometry and magnetic resonance spectroscopy analyses of metabolites after incubation of cells with [1‐(13)C]lactate or [1,2‐(13)C]glucose, respectively, demonstrated that anaplerotic pyruvate carboxylation, which was thought to be exclusive to astrocytes, is also active in oligodendrocytes. Using [1,2‐(13)C]acetate, we show that oligodendrocytes convert acetate into acetyl CoA which is metabolized in the tricarboxylic acid cycle. Analysis of labelling patterns of alanine after incubation of cells with [1,2‐(13)C]acetate and [1,2‐(13)C]glucose showed catabolic oxidation of malate or oxaloacetate. In conclusion, we report that oligodendrocyte lineage cells at late differentiation stages are metabolically highly active cells that are likely to contribute considerably to the metabolic activity of the CNS. GLIA 2016;64:21–34 |
format | Online Article Text |
id | pubmed-4832329 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-48323292016-04-20 Characterization of glucose‐related metabolic pathways in differentiated rat oligodendrocyte lineage cells Amaral, Ana I. Hadera, Mussie G. Tavares, Joana M. Kotter, Mark R. N. Sonnewald, Ursula Glia Research Articles Although oligodendrocytes constitute a significant proportion of cells in the central nervous system (CNS), little is known about their intermediary metabolism. We have, therefore, characterized metabolic functions of primary oligodendrocyte precursor cell cultures at late stages of differentiation using isotope‐labelled metabolites. We report that differentiated oligodendrocyte lineage cells avidly metabolize glucose in the cytosol and pyruvate derived from glucose in the mitochondria. The labelling patterns of metabolites obtained after incubation with [1,2‐(13)C]glucose demonstrated that the pentose phosphate pathway (PPP) is highly active in oligodendrocytes (approximately 10% of glucose is metabolized via the PPP as indicated by labelling patterns in phosphoenolpyruvate). Mass spectrometry and magnetic resonance spectroscopy analyses of metabolites after incubation of cells with [1‐(13)C]lactate or [1,2‐(13)C]glucose, respectively, demonstrated that anaplerotic pyruvate carboxylation, which was thought to be exclusive to astrocytes, is also active in oligodendrocytes. Using [1,2‐(13)C]acetate, we show that oligodendrocytes convert acetate into acetyl CoA which is metabolized in the tricarboxylic acid cycle. Analysis of labelling patterns of alanine after incubation of cells with [1,2‐(13)C]acetate and [1,2‐(13)C]glucose showed catabolic oxidation of malate or oxaloacetate. In conclusion, we report that oligodendrocyte lineage cells at late differentiation stages are metabolically highly active cells that are likely to contribute considerably to the metabolic activity of the CNS. GLIA 2016;64:21–34 John Wiley and Sons Inc. 2015-09-09 2016-01 /pmc/articles/PMC4832329/ /pubmed/26352325 http://dx.doi.org/10.1002/glia.22900 Text en © 2015 The Authors. Glia Published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution (http://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 Amaral, Ana I. Hadera, Mussie G. Tavares, Joana M. Kotter, Mark R. N. Sonnewald, Ursula Characterization of glucose‐related metabolic pathways in differentiated rat oligodendrocyte lineage cells |
title | Characterization of glucose‐related metabolic pathways in differentiated rat oligodendrocyte lineage cells |
title_full | Characterization of glucose‐related metabolic pathways in differentiated rat oligodendrocyte lineage cells |
title_fullStr | Characterization of glucose‐related metabolic pathways in differentiated rat oligodendrocyte lineage cells |
title_full_unstemmed | Characterization of glucose‐related metabolic pathways in differentiated rat oligodendrocyte lineage cells |
title_short | Characterization of glucose‐related metabolic pathways in differentiated rat oligodendrocyte lineage cells |
title_sort | characterization of glucose‐related metabolic pathways in differentiated rat oligodendrocyte lineage cells |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4832329/ https://www.ncbi.nlm.nih.gov/pubmed/26352325 http://dx.doi.org/10.1002/glia.22900 |
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