Sphingosine-1-phosphate inhibits IL-1-induced expression of C-C motif ligand 5 via c-Fos-dependent suppression of IFN-β amplification loop

FASEB J. 2015 Dec;29(12):4853-65. doi: 10.1096/fj.15-275180. Epub 2015 Aug 5.

Abstract

The neuroinflammation associated with multiple sclerosis involves activation of astrocytes that secrete and respond to inflammatory mediators such as IL-1. IL-1 stimulates expression of many chemokines, including C-C motif ligand (CCL) 5, that recruit immune cells, but it also stimulates sphingosine kinase-1, an enzyme that generates sphingosine-1-phosphate (S1P), a bioactive lipid mediator essential for inflammation. We found that whereas S1P promotes IL-1-induced expression of IL-6, it inhibits IL-1-induced CCL5 expression in astrocytes. This inhibition is mediated by the S1P receptor (S1PR)-2 via an inhibitory G-dependent mechanism. Consistent with this surprising finding, infiltration of macrophages into sites of inflammation increased significantly in S1PR2(-/-) animals. However, activation of NF-κB, IFN regulatory factor-1, and MAPKs, all of which regulate CCL5 expression in response to IL-1, was not diminished by the S1P in astrocytes. Instead, S1PR2 stimulated inositol 1,4,5-trisphosphate-dependent Ca(++) release and Elk-1 phosphorylation and enhanced c-Fos expression. In our study, IL-1 induced the IFNβ production that supports CCL5 expression. An intriguing finding was that S1P induced c-Fos-inhibited CCL5 directly and also indirectly through inhibition of the IFN-β amplification loop. We propose that in addition to S1PR1, which promotes inflammation, S1PR2 mediates opposing inhibitory functions that limit CCL5 expression and diminish the recruitment of immune cells.

Keywords: GPCR; astrocytes; chemokines; inflammation.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Cells, Cultured
  • Chemokine CCL5 / antagonists & inhibitors*
  • Humans
  • Interferon Regulatory Factor-1 / biosynthesis
  • Interferon-beta / biosynthesis
  • Interferon-beta / metabolism*
  • Interleukin-1 / antagonists & inhibitors*
  • Ligands
  • Lysophospholipids / physiology*
  • Mice
  • Mice, Knockout
  • Phosphorylation
  • Protein Kinases / metabolism
  • Proto-Oncogene Proteins c-fos / metabolism*
  • STAT1 Transcription Factor / metabolism
  • STAT2 Transcription Factor / metabolism
  • Sphingosine / analogs & derivatives*
  • Sphingosine / physiology

Substances

  • Ccl5 protein, mouse
  • Chemokine CCL5
  • IRF1 protein, human
  • Interferon Regulatory Factor-1
  • Interleukin-1
  • Ligands
  • Lysophospholipids
  • Proto-Oncogene Proteins c-fos
  • STAT1 Transcription Factor
  • STAT1 protein, human
  • STAT2 Transcription Factor
  • STAT2 protein, human
  • sphingosine 1-phosphate
  • Interferon-beta
  • Protein Kinases
  • Sphingosine