The Intra-nuclear SphK2-S1P Axis Facilitates M1-to-M2 Shift of Microglia via Suppressing HDAC1-Mediated KLF4 Deacetylation

Front Immunol. 2019 Jun 4:10:1241. doi: 10.3389/fimmu.2019.01241. eCollection 2019.

Abstract

Sphingosine 1-phosphate (S1P) is involved in a variety of cellular responses including microglial activation and polarization. However, the impacts of S1P on ischemia-induced microglial activation and polarization remain unclear. In the present study, Sprague-Dawley rats were selected for middle cerebral artery occlusion (MCAO) establishment and treated with S1P analog FTY720 (0.5, 1, 2 mg/kg) for 24 h. The impacts of FTY720 on oxygen-glucose deprivation (OGD)-induced microglial polarization were examined in the primary cultured microglia. FTY720 treatment could prevent ischemia-induced brain injury and neurological dysfunction, also decrease the levels of IL-1β and TNF-α and promote M2 microglial polarization in rats. Further, we found that FTY720 inhibited the expressions of M1 markers, but increased the expressions of M2 markers in the OGD-insulted microglia. And FTY720 could enhance the phagocytic function of microglia. The sphingosine kinase 1/2 (SphK1/2) or the Sphk2 inhibitor could prevent the M1 to M2 phenotype shift improved by FTY720, but the Sphk1 inhibitor failed to affect the roles of FTY720. Furthermore, the Sphk1/2 or Sphk2 inhibitor promoted the activities of histone deacetylase (HDAC1) and inhibited the histone acetylation of the Krüppel-like factor 4 (KLF4) promoter regions, indicating that intra-nuclear pFTY720 inhibited HDAC1 activations and prevented KLF4 to interact with HDAC1, and thereby suppresses KLF4 deacetylation. Therefore, our data reveals that intra-nuclear SphK2-S1P axis might facilitate the transformation of microglial polarization from M1 to M2 phenotype, which might be intra-nuclear regulatory mechanisms of FTY720-prevented neuroinflammation.

Keywords: KLF4; S1P; Sphk2; ischemia; microglial polarization.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylation
  • Animals
  • Brain Injuries / etiology
  • Brain Injuries / metabolism
  • Brain Injuries / pathology
  • Cell Plasticity
  • Cells, Cultured
  • Fingolimod Hydrochloride / pharmacology
  • Glucose / metabolism
  • Histone Deacetylase 1 / metabolism*
  • Inflammation Mediators / metabolism
  • Kruppel-Like Factor 4
  • Kruppel-Like Transcription Factors / metabolism*
  • Lysophospholipids / metabolism*
  • Microglia / immunology*
  • Microglia / metabolism*
  • Oxidation-Reduction
  • Oxygen / metabolism
  • Phagocytosis
  • Phenotype
  • Phosphorylation
  • Phosphotransferases (Alcohol Group Acceptor) / metabolism*
  • Promoter Regions, Genetic
  • RNA, Small Interfering / genetics
  • Rats
  • Signal Transduction*
  • Sphingosine / analogs & derivatives*
  • Sphingosine / metabolism

Substances

  • Inflammation Mediators
  • Klf4 protein, rat
  • Kruppel-Like Factor 4
  • Kruppel-Like Transcription Factors
  • Lysophospholipids
  • RNA, Small Interfering
  • sphingosine 1-phosphate
  • Phosphotransferases (Alcohol Group Acceptor)
  • Histone Deacetylase 1
  • Fingolimod Hydrochloride
  • Glucose
  • Sphingosine
  • Oxygen