Abstract
Osteopontin (OPN) is a key immunoregulator in the autoimmune-mediated demyelinating disease multiple sclerosis. OPN may also play a role in the remyelination since it is 1) a ligand for αV integrins, several of which regulate the properties of the oligodendrocyte precursor cells (OPCs) primarily responsible for remyelination, and 2) enhances myelin membrane formation in OPC lines. Here we show that OPN is expressed at high levels during remyelination of toxin-induced demyelination. The increased expression is due to mRNA expression in macrophages and follows differences in macrophage responses to demyelination in young and old adult animals. To identify the role of OPN in remyelination focal demyelination was induced in wild-type and OPN-/- mice. There was no difference in the rate of remyelination between the two groups indicating that OPN is not a critical component of remyelination.
Original language | English |
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Pages (from-to) | 209-217 |
Number of pages | 9 |
Journal | Neurobiology of Disease |
Volume | 31 |
Issue number | 2 |
Early online date | 4 May 2008 |
DOIs | |
Publication status | Published - Aug 2008 |
Keywords
- Demyelination
- Knockout
- Multiple sclerosis
- Myelin
- Oligodendrocyte precursor cell
- Osteopontin
- Regeneration
- Remyelination