Fingolimod induces neuroprotective factors in human astrocytes

J Neuroinflammation. 2015 Sep 30:12:184. doi: 10.1186/s12974-015-0393-6.

Abstract

Background: Fingolimod (FTY720) is the first sphingosine-1-phosphate (S1P) receptor modulator approved for the treatment of multiple sclerosis. The phosphorylated active metabolite FTY720-phosphate (FTY-P) interferes with lymphocyte trafficking. In addition, it accumulates in the CNS and reduces brain atrophy in multiple sclerosis (MS), and neuroprotective effects are hypothesized.

Methods: Human primary astrocytes as well as human astrocytoma cells were stimulated with FTY-P or S1P. We analyzed gene expression by a genome-wide microarray and validated induced candidate genes by quantitative PCR (qPCR) and ELISA. To identify the S1P-receptor subtypes involved, we applied a membrane-impermeable S1P analog (dihydro-S1P), receptor subtype specific agonists and antagonists, as well as RNAi silencing.

Results: FTY-P induced leukemia inhibitory factor (LIF), interleukin 11 (IL11), and heparin-binding EGF-like growth factor (HBEGF) mRNA, as well as secretion of LIF and IL11 protein. In order to mimic an inflammatory milieu as observed in active MS lesions, we combined FTY-P application with tumor necrosis factor (TNF). In the presence of this key inflammatory cytokine, FTY-P synergistically induced LIF, HBEGF, and IL11 mRNA, as well as secretion of LIF and IL11 protein. TNF itself induced inflammatory, B-cell promoting, and antiviral factors (CXCL10, BAFF, MX1, and OAS2). Their induction was blocked by FTY-P. After continuous exposure of cells to FTY-P or S1P for up to 7 days, the extent of induction of neurotrophic factors and the suppression of TNF-induced inflammatory genes declined but was still detectable. The induction of neurotrophic factors was mediated via surface S1P receptors 1 (S1PR1) and 3 (S1PR3).

Conclusions: We identified effects of FTY-P on astrocytes, namely induction of neurotrophic mediators (LIF, HBEGF, and IL11) and inhibition of TNF-induced inflammatory genes (CXCL10, BAFF, MX1, and OAS2). This supports the view that a part of the effects of fingolimod may be mediated via astrocytes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Astrocytes / drug effects*
  • Chemokine CXCL10 / genetics
  • Chemokine CXCL10 / metabolism
  • Corpus Striatum / cytology
  • Dose-Response Relationship, Drug
  • Enzyme-Linked Immunosorbent Assay
  • Fetus / cytology
  • Fingolimod Hydrochloride / pharmacology*
  • Heparin-binding EGF-like Growth Factor / genetics
  • Heparin-binding EGF-like Growth Factor / metabolism
  • Humans
  • Interleukin-11 / genetics
  • Interleukin-11 / metabolism
  • Lysophospholipids / pharmacology
  • Microarray Analysis
  • NF-kappa B / genetics
  • NF-kappa B / metabolism
  • Neural Stem Cells / drug effects*
  • Neuroprotective Agents / pharmacology*
  • RNA, Messenger
  • RNA, Small Interfering / pharmacology
  • Sphingosine / analogs & derivatives
  • Sphingosine / pharmacology
  • Time Factors

Substances

  • Chemokine CXCL10
  • HBEGF protein, human
  • Heparin-binding EGF-like Growth Factor
  • Interleukin-11
  • Lysophospholipids
  • NF-kappa B
  • Neuroprotective Agents
  • RNA, Messenger
  • RNA, Small Interfering
  • sphingosine 1-phosphate
  • Fingolimod Hydrochloride
  • Sphingosine