Dr GRAHAM SHERIDAN GRAHAM.SHERIDAN@NOTTINGHAM.AC.UK
Assistant Professor
S1P1 receptor subtype inhibits demyelination and regulates chemokine release in cerebellar slice cultures
Sheridan, Graham K.; Dev, Kumlesh K.
Authors
Kumlesh K. Dev
Contributors
Dr GRAHAM SHERIDAN GRAHAM.SHERIDAN@NOTTINGHAM.AC.UK
Researcher
Abstract
Sphingosine-1-phosphate receptors (S1PRs) are drug targets for the compound FTY720, which is the first oral therapy developed for treatment of relapsing-remitting multiple sclerosis. S1PRs play a variety of functional roles in the differentiation, proliferation, survival and/or migration of neurons and glia. In this study, rat organotypic cerebellar slice cultures were used to assess whether S1PRs play a role in demyelination induced by lysolecithin (LPC). The data demonstrated that FTY720 and SEW2871 (a S1P1R-specific agonist) inhibited LPC-induced demyelination as assessed by myelin basic protein (MBP) immunofluorescence. Treatment with both drugs for 48 h also induced an increase in S1P1R expression in astrocytes. Moreover, FTY720 and SEW2871 inhibited the release of several chemokines in conditions of LPC-induced demyelination, including LIX (CXCL5), MIP-1alpha, and MIP-3alpha. Taken together, the data suggest that activation of S1P1Rs prevents LPC-induced demyelination via a mechanism involving a reduction of chemotactic chemokine release. The study supports the concept that FTY720 attenuates demyelination by not only preventing S1PR-mediated T cell migration into the CNS but also by limiting cytokine communication between cells of the immune system and the CNS. © 2011 Wiley Periodicals, Inc.
Citation
Sheridan, G. K., & Dev, K. K. (2012). S1P1 receptor subtype inhibits demyelination and regulates chemokine release in cerebellar slice cultures. Glia, 60(3), 382-392. https://doi.org/10.1002/glia.22272
Journal Article Type | Article |
---|---|
Acceptance Date | Nov 1, 2011 |
Online Publication Date | Nov 22, 2011 |
Publication Date | 2012-03 |
Deposit Date | Aug 16, 2022 |
Journal | GLIA |
Print ISSN | 0894-1491 |
Electronic ISSN | 1098-1136 |
Publisher | Wiley |
Peer Reviewed | Peer Reviewed |
Volume | 60 |
Issue | 3 |
Pages | 382-392 |
DOI | https://doi.org/10.1002/glia.22272 |
Public URL | https://nottingham-repository.worktribe.com/output/10076734 |
Publisher URL | https://onlinelibrary.wiley.com/doi/10.1002/glia.22272 |
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