An animal model for late onset chronic demyelination disease caused by failed terminal differentiation of oligodendrocytes

Jianmei Ma, Michio Matsumoto, Kenji F. Tanaka, Hirohide Takebayashi, Kazuhiro Ikenaka

Research output: Contribution to journalArticle

29 Citations (Scopus)

Abstract

Various animal models are available for studying human multiple sclerosis (MS). Most of them model the initial phase of MS, including the immune-triggered attack of the myelin membrane and/or oligodendrocytes and, occasionally, demonstrate the remission and relapsing phases. However, few mimic the late chronic demyelinating phase. Overexpression of the proteolipid protein gene (Plp) causes a unique demyelinating disorder in mice in which normal-appearing myelin forms early in life and chronic demyelination occurs later. We found that remyelination is severely affected in this late demyelinating phase, but is not caused by deprivation of oligodendrocyte progenitors expressing PDGF receptor alpha (PDGFRα) and Olig2, which are present at an even higher number in the demyelinated white matter of the mutants than in wild-type controls. Furthermore, mature oligodendrocytes containing PLP were observed, but failed to remyelinate. The ability of oligodendrocytes from older transgenic animals to produce a myelin membrane-like structure was not impaired when cultured in vitro, which indicates that the lack of remyelination is not simply caused by changes in the intrinsic properties of the oligodendrocytes. Glial activation also occurred much earlier than active demyelination in mutant mice. Thus, in addition to intrinsic mechanisms, extrinsic mechanisms might also have an important role in defects of remyelination. These features are also observed in patients at a late stage of MS, leading to chronic demyelinating lesions. Thus, this mouse model partly mimics the late stage of MS and can be used to study the cause of inhibition of remyelination.

Original languageEnglish
Pages (from-to)81-91
Number of pages11
JournalNeuron Glia Biology
Volume2
Issue number2
DOIs
Publication statusPublished - 2006 May 1
Externally publishedYes

Keywords

  • Glial activation
  • Neuropathology
  • Oligodendrocyte
  • Oligodendrocyte progenitor
  • Proteolipid protein

ASJC Scopus subject areas

  • Cellular and Molecular Neuroscience
  • Cell Biology

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