Cited by 109Neurogenesis and neuroplasticity mechanismsNeuroscience and Neuropharmacology ResearchNeuroinflammation and Neurodegeneration Mechanisms

Adapting brain metabolism to myelination and long‐range signal transduction

Hirrlinger, Johannes, Nave, Klaus‐Armin·2014·Glia

Abstract

In the mammalian brain, the subcortical white matter comprises long-range axonal projections and their associated glial cells. Here, astrocytes and oligodendrocytes serve specific functions during development and throughout adult life, when they meet the metabolic needs of long fiber tracts. Within a short period of time, oligodendrocytes generate large amount of lipids, such as cholesterol, and membrane proteins for building the myelin sheaths. After myelination has been completed, a remaining function of glial metabolism is the energetic support of axonal transport and impulse propagation. Astrocytes can support axonal energy metabolism under low glucose conditions by the degradation of stored glycogen. Recently it has been recognized that the ability of glycolytic oligodendrocytes to deliver pyruvate and lactate is critical for axonal functions in vivo. In this review, we discuss the specific demands of oligodendrocytes during myelination and potential routes of metabolites between glial cells and myelinated axons. As examples, four specific metabolites are highlighted (cholesterol, glycogen, lactate, and N-acetyl-aspartate) that contribute to the specific functions of white matter glia. Regulatory processes are discussed that could be involved in coordinating metabolic adaptations and in providing feedback information about metabolic states.

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Crossref · 10.1002/glia.22737

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References 156 · Cited by 109

Authors
Hirrlinger, J., & Nave, K.
Affiliations
Max Planck Institute of Experimental Medicine (DE)
Corresponding author
Hirrlinger, Johannes
Venue
Glia
Publisher
Wiley
Published
2014-08-06
Volume
62
Issue
11
Pages
1749-1761
ISSN
  • 0894-1491 (ISSN-L)
  • 1098-1136
OpenAlex
W1495776408
Cited by
109
References
156
Citations by year
2026: 6 · 2025: 4 · 2024: 4 · 2023: 7 · 2022: 11 · 2021: 9 · 2020: 11 · 2019: 7 · 2018: 8 · 2017: 15 · 2016: 17 · 2015: 9 · 2014: 1
FWCI
4.87
Type
journal article
Language
en
Open access
closed
Locations
  • Glia (publishedVersion)
  • PubMed (publishedVersion)
  • Max Planck Institute for Plasma Physics (submittedVersion)
  • MPG.PuRe (Max Planck Society) (submittedVersion)
Funders
  • DFG (Hi1414/1-1 and Hi1414/2-1)
  • German Diabetes Society
  • DFG Research Center “Nanoscale Microscopy and Molecular Physiology of the Brain” (SFB-TR43, EU-FP7 (Leukotreat, Ngidd))
  • BMBF (Leukonet), Oliver's Army, and an ERC Advanced Grant (AxoGlia)
Topics
  • Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
  • Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
Keywords
oligodendrocytes, astrocytes, myelination, white matter, glial metabolism, axonal energy metabolism, cholesterol, glycogen, lactate, N-acetylaspartate, axonal transport, impulse propagation
MeSH terms
Adaptation, Physiological, Animals, Brain, Energy Metabolism, Humans, Myelin Sheath, Signal Transduction

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