Cited by 72Metabolism and Genetic DisordersLysosomal Storage Disorders ResearchHereditary Neurological Disorders

Myelin peroxisomes–Essential organelles for the maintenance of white matter in the nervous system

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Kassmann, Celia M.·2014·Biochimie

Abstract

Peroxisomes are cellular compartments primarily associated with lipid metabolism. Most cell types, including nervous system cells, harbor several hundred of these organelles. The importance of peroxisomes for central nervous system white matter is evidenced by a variety of human peroxisomal disorders with neurological impairment frequently involving the white matter. Moreover, the most frequent childhood white matter disease, X-linked adrenoleukodystrophy, is a peroxisomal disorder. During the past decade advances in imaging techniques have enabled the identification of peroxisomes within the myelin sheath, especially close to nodes of Ranvier. Although the function of myelin peroxisomes is not solved yet on molecular level, recently acquired knowledge suggests a central role for these organelles in axo-glial metabolism. This review focuses on the biology of myelin peroxisomes as well as on the pathology of myelin and myelinated axons that is observed as a consequence of partial or complete peroxisomal dysfunction in the brain.

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Crossref · 10.1016/j.biochi.2013.09.020

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  • Peroxisomes are few in neuron perikarya or dendrites, rare within axons, and absent in synaptic terminals in the spinal cord except during early development.

    “While mitochondria fill dendrites and axons, peroxisomes are few in neuron perikarya or dendrites, rare within axons [251,253,254,255,292,293], and absent in synaptic terminals in the spinal cord [255] except during early development [255].”

    From Revisiting the Pathogenesis of X-Linked Adrenoleukodystrophy (2025) · cites this paper as [253]

  • Microglia have abundant peroxisome content and express abundant ALDP in normal microglia in human and mouse brains.

    “Their peroxisome content is abundant [166,253,315], and they express abundant ALDP in normal microglia in human and mouse brains [156].”

    From Revisiting the Pathogenesis of X-Linked Adrenoleukodystrophy (2025) · cites this paper as [253]

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References 83 · Cited by 72

Authors
Kassmann, C. M.
Affiliations
Max Planck Institute of Experimental Medicine (DE)
Corresponding author
Kassmann, Celia M.
Venue
Biochimie
Publisher
Elsevier BV
Published
2014-03
Volume
98
Pages
111-118
ISSN
  • 0037-9042 (ISSN-L)
  • 0300-9084
OpenAlex
W2078916751
Cited by
72
References
83
Citations by year
2026: 7 · 2025: 7 · 2024: 11 · 2023: 9 · 2022: 10 · 2021: 7 · 2020: 6 · 2019: 2 · 2018: 2 · 2017: 1 · 2016: 6 · 2015: 3 · 2014: 1
FWCI
0.35
Type
journal article
Language
en
Open access
Locations
  • Biochimie (publishedVersion, cc-by-nc-nd)
  • PubMed (publishedVersion)
  • Max Planck Institute for Plasma Physics (submittedVersion)
  • MPG.PuRe (Max Planck Society) (submittedVersion)
Funders
  • “Olivers Army” (England)
  • “The Myelin Project” (USA/Germany)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Clinical Biochemistry › Metabolism and Genetic Disorders
  • Health Sciences › Medicine › Physiology › Lysosomal Storage Disorders Research
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Hereditary Neurological Disorders
Keywords
peroxisomes, white matter, peroxisomal disorders, X-linked adrenoleukodystrophy, myelin sheath, nodes of Ranvier, myelin pathology, myelinated axons, lipid metabolism
MeSH terms
Adrenoleukodystrophy, Animals, Axons, Humans, Myelin Sheath, Neuroglia, Peroxisomal Disorders, Peroxisomes, Mice

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