The neurobiology of sphingosine 1-phosphate signaling and sphingosine 1-phosphate receptor modulators

被引:90
|
作者
Soliven, Betty [1 ]
Miron, Veronique [2 ]
Chun, Jerold [3 ]
机构
[1] Univ Chicago, Dept Neurol, Chicago, IL 60637 USA
[2] Univ Edinburgh, Ctr MS Res, Queens Med Res Inst, Edinburgh, Midlothian, Scotland
[3] Scripps Res Inst, Dept Mol Biol, La Jolla, CA 92037 USA
关键词
EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; RELAPSING MULTIPLE-SCLEROSIS; SPHINGOSINE-1-PHOSPHATE RECEPTORS; FINGOLIMOD FTY720; ORAL FINGOLIMOD; NERVOUS-SYSTEM; OLIGODENDROCYTE PROGENITORS; MATURE OLIGODENDROCYTES; S1P RECEPTORS; RAT MODEL;
D O I
10.1212/WNL.0b013e31820d9507
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Sphingosine 1-phosphate receptors (S1PRs) are G protein-coupled receptors expressed by many cell types, including immune and neural cells. These receptors are promising targets for immunomodulatory and possibly neuromodulatory therapies. Fingolimod (FTY720) is a sphingosine analog that, when phosphorylated, becomes a prototypical S1PR modulator. It has recently been approved as the first oral treatment for relapsing forms of multiple sclerosis in some countries. Fingolimod has documented effects on lymphocyte egress, selectively retaining lymphocytes within the lymph nodes. In addition, fingolimod can enter the CNS and can act on S1PRs expressed by most neural lineages. In this article, we discuss recent results supporting the concept that S1PR modulators may exert neuroprotective and regenerative actions in the CNS as well as having anti-inflammatory effects. NEUROLOGY 2011;76 (Suppl 3):S9-S14
引用
收藏
页码:S9 / S14
页数:6
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