Adapting brain metabolism to myelination and long‐range signal transduction
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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The supplies of cholesterol and fatty acid de novo are often the rate limiting factor of myelin formation.
“The supplies of cholesterol and fatty acid de novo are therefore often the rate limiting factor of myelin formation (Hirrlinger & Nave 2014).”
From Apolipoprotein E ε4 disrupts oligodendrocyte differentiation by interfering with astrocyte‐derived lipid transport (2023) · cites this paper as Hirrlinger & Nave 2014
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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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