Cargando…

Neural Stem Cells in the Adult Subventricular Zone Oxidize Fatty Acids to Produce Energy and Support Neurogenic Activity

Neural activity is tightly coupled to energy consumption, particularly sugars such as glucose. However, we find that, unlike mature neurons and astrocytes, neural stem/progenitor cells (NSPCs) do not require glucose to sustain aerobic respiration. NSPCs within the adult subventricular zone (SVZ) exp...

Descripción completa

Detalles Bibliográficos
Autores principales: Stoll, Elizabeth A., Makin, Rebecca, Sweet, Ian R., Trevelyan, Andrew J., Miwa, Satomi, Horner, Philip J., Turnbull, Douglass M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4478223/
https://www.ncbi.nlm.nih.gov/pubmed/25919237
http://dx.doi.org/10.1002/stem.2042
_version_ 1782377858288582656
author Stoll, Elizabeth A.
Makin, Rebecca
Sweet, Ian R.
Trevelyan, Andrew J.
Miwa, Satomi
Horner, Philip J.
Turnbull, Douglass M.
author_facet Stoll, Elizabeth A.
Makin, Rebecca
Sweet, Ian R.
Trevelyan, Andrew J.
Miwa, Satomi
Horner, Philip J.
Turnbull, Douglass M.
author_sort Stoll, Elizabeth A.
collection PubMed
description Neural activity is tightly coupled to energy consumption, particularly sugars such as glucose. However, we find that, unlike mature neurons and astrocytes, neural stem/progenitor cells (NSPCs) do not require glucose to sustain aerobic respiration. NSPCs within the adult subventricular zone (SVZ) express enzymes required for fatty acid oxidation and show sustained increases in oxygen consumption upon treatment with a polyunsaturated fatty acid. NSPCs also demonstrate sustained decreases in oxygen consumption upon treatment with etomoxir, an inhibitor of fatty acid oxidation. In addition, etomoxir decreases the proliferation of SVZ NSPCs without affecting cellular survival. Finally, higher levels of neurogenesis can be achieved in aged mice by ectopically expressing proliferator‐activated receptor gamma coactivator 1 alpha (PGC1α), a factor that increases cellular aerobic capacity by promoting mitochondrial biogenesis and metabolic gene transcription. Regulation of metabolic fuel availability could prove a powerful tool in promoting or limiting cellular proliferation in the central nervous system. Stem Cells 2015;33:2306–2319
format Online
Article
Text
id pubmed-4478223
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-44782232016-06-24 Neural Stem Cells in the Adult Subventricular Zone Oxidize Fatty Acids to Produce Energy and Support Neurogenic Activity Stoll, Elizabeth A. Makin, Rebecca Sweet, Ian R. Trevelyan, Andrew J. Miwa, Satomi Horner, Philip J. Turnbull, Douglass M. Stem Cells Tissue‐Specific Stem Cells Neural activity is tightly coupled to energy consumption, particularly sugars such as glucose. However, we find that, unlike mature neurons and astrocytes, neural stem/progenitor cells (NSPCs) do not require glucose to sustain aerobic respiration. NSPCs within the adult subventricular zone (SVZ) express enzymes required for fatty acid oxidation and show sustained increases in oxygen consumption upon treatment with a polyunsaturated fatty acid. NSPCs also demonstrate sustained decreases in oxygen consumption upon treatment with etomoxir, an inhibitor of fatty acid oxidation. In addition, etomoxir decreases the proliferation of SVZ NSPCs without affecting cellular survival. Finally, higher levels of neurogenesis can be achieved in aged mice by ectopically expressing proliferator‐activated receptor gamma coactivator 1 alpha (PGC1α), a factor that increases cellular aerobic capacity by promoting mitochondrial biogenesis and metabolic gene transcription. Regulation of metabolic fuel availability could prove a powerful tool in promoting or limiting cellular proliferation in the central nervous system. Stem Cells 2015;33:2306–2319 John Wiley and Sons Inc. 2015-07 2015-06-04 /pmc/articles/PMC4478223/ /pubmed/25919237 http://dx.doi.org/10.1002/stem.2042 Text en © 2015 The Authors. STEM CELLS published by Wiley Periodicals, Inc. on behalf of AlphaMed Press 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 Tissue‐Specific Stem Cells
Stoll, Elizabeth A.
Makin, Rebecca
Sweet, Ian R.
Trevelyan, Andrew J.
Miwa, Satomi
Horner, Philip J.
Turnbull, Douglass M.
Neural Stem Cells in the Adult Subventricular Zone Oxidize Fatty Acids to Produce Energy and Support Neurogenic Activity
title Neural Stem Cells in the Adult Subventricular Zone Oxidize Fatty Acids to Produce Energy and Support Neurogenic Activity
title_full Neural Stem Cells in the Adult Subventricular Zone Oxidize Fatty Acids to Produce Energy and Support Neurogenic Activity
title_fullStr Neural Stem Cells in the Adult Subventricular Zone Oxidize Fatty Acids to Produce Energy and Support Neurogenic Activity
title_full_unstemmed Neural Stem Cells in the Adult Subventricular Zone Oxidize Fatty Acids to Produce Energy and Support Neurogenic Activity
title_short Neural Stem Cells in the Adult Subventricular Zone Oxidize Fatty Acids to Produce Energy and Support Neurogenic Activity
title_sort neural stem cells in the adult subventricular zone oxidize fatty acids to produce energy and support neurogenic activity
topic Tissue‐Specific Stem Cells
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4478223/
https://www.ncbi.nlm.nih.gov/pubmed/25919237
http://dx.doi.org/10.1002/stem.2042
work_keys_str_mv AT stollelizabetha neuralstemcellsintheadultsubventricularzoneoxidizefattyacidstoproduceenergyandsupportneurogenicactivity
AT makinrebecca neuralstemcellsintheadultsubventricularzoneoxidizefattyacidstoproduceenergyandsupportneurogenicactivity
AT sweetianr neuralstemcellsintheadultsubventricularzoneoxidizefattyacidstoproduceenergyandsupportneurogenicactivity
AT trevelyanandrewj neuralstemcellsintheadultsubventricularzoneoxidizefattyacidstoproduceenergyandsupportneurogenicactivity
AT miwasatomi neuralstemcellsintheadultsubventricularzoneoxidizefattyacidstoproduceenergyandsupportneurogenicactivity
AT hornerphilipj neuralstemcellsintheadultsubventricularzoneoxidizefattyacidstoproduceenergyandsupportneurogenicactivity
AT turnbulldouglassm neuralstemcellsintheadultsubventricularzoneoxidizefattyacidstoproduceenergyandsupportneurogenicactivity