Cited by 149Multiple Sclerosis Research StudiesNeuroinflammation and Neurodegeneration MechanismsPeripheral Neuropathies and Disorders

Oligodendrocytes and the early multiple sclerosis lesion

Prineas, John W., Parratt, John D. E.·2012·Annals of Neurology

Abstract

There is little agreement among neuropathologists regarding the timing and nature of oligodendrocyte loss in multiple sclerosis (MS). This review describes changes that accompany acute oligodendrocyte loss in new lesions. Included is a description of the immunopathology of new lesions in 23 severe early cases selected from a bank of 300 MS autopsies. Oligodendrocytes in prephagocytic lesions exhibit cytopathic changes that include apoptosis of oligodendrocytes immunoreactive for caspase 3, phagocytosis of apoptotic oligodendrocytes, swelling of cells with abnormal nuclei, complement deposition, and lysis. These are nonspecific changes that provide no clue as to the cause of oligodendrocyte injury. Associated changes include the presence of enlarged immunoglobulin (IgG)(+) microglia and early macrophages, the presence nearby of a focus of inflammatory demyelination, an open blood-brain barrier, and the presence of rare CD8 T cells. Myelin contacted by IgG(+) macrophages is immunoreactive for complement but not for IgG. It is likely that macrophage activity in evolving white and gray matter plaques is scavenging activity directed at nonvital myelin secondary to oligodendrocytes loss. One feature of MS that is not understood is the extraordinarily close resemblance the disease shows pathologically to neuromyelitis optica (NMO), including that demyelination in both is secondary to a loss of caspase 3-positive apoptotic oligodendrocytes. These similarities raise the possibility th…

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Crossref · 10.1002/ana.23634

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  • Myelin breakdown in multiple sclerosis invariably originated around parenchymal blood vessels.

    “Seminal characterization of the MS lesion by Dawson in 1916 recognized that myelin breakdown invariably originated around parenchymal blood vessels (483).”

    From Blood-Brain Barrier: From Physiology to Disease and Back (2019) · cites this paper as [483]

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Authors
Prineas, J. W., & Parratt, J. D. E.
Affiliations
The University of Sydney (AU)
Corresponding author
Prineas, John W.
Venue
Annals of Neurology
Publisher
Wiley
Published
2012-07
Volume
72
Issue
1
Pages
18-31
ISSN
  • 0364-5134 (ISSN-L)
  • 1531-8249
OpenAlex
W2101489349
Cited by
149
References
5
Citations by year
2026: 2 · 2025: 10 · 2024: 12 · 2023: 8 · 2022: 8 · 2021: 10 · 2020: 5 · 2019: 13 · 2018: 11 · 2017: 9 · 2016: 13 · 2015: 16 · 2014: 15 · 2013: 16 · 2012: 1
FWCI
2.22
Type
journal article
Language
en
Open access
closed
Locations
  • Annals of Neurology (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Pathology and Forensic Medicine › Multiple Sclerosis Research Studies
  • Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
  • Health Sciences › Medicine › Neurology › Peripheral Neuropathies and Disorders
Keywords
multiple sclerosis, oligodendrocyte loss, oligodendrocyte apoptosis, caspase-3, demyelination, macrophages, microglia, complement deposition, IgG, neuromyelitis optica, autoimmune disease, early lesions, CD8+ T cells, blood-brain barrier
MeSH terms
Blood-Brain Barrier, Humans, Multiple Sclerosis, Myelin Sheath, Nerve Fibers, Myelinated, Oligodendroglia

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