Distribution of sphingosine kinase activity and mRNA in rodent brain

  • Nicolas Blondeau
  • , Yushuan Lai
  • , Sarah Tyndall
  • , Margherita Popolo
  • , Kamil Topalkara
  • , James K. Pru
  • , Ling Zhang
  • , Hyunghwan Kim
  • , James K. Liao
  • , Kan Ding
  • , Christian Waeber

Research output: Contribution to journalArticlepeer-review

Abstract

Sphingosine-1-phosphate (S1P) is a lipid mediator that exerts multiple cellular functions through activation of a subfamily of G-protein-coupled receptors. Although there is evidence that S1P plays a role in the developing and adult CNS, little is known about the ability of brain parenchyma to synthesize this lipid. We have therefore analyzed the brain distribution of the enzymatic activity of the S1P synthesizing enzyme, sphingosine kinase (SPHK) [EC:2.7.1.91], as well as mRNA distribution for one of the two isoforms of this enzyme, sphingosine kinase 2. SPHK activity, measured by the conversion of [3H]sphingosine to [3H]S1P, is highest in cerebellum, followed by cortex and brainstem. Lowest activities were found in striatum and hippocampus. Sensitivity to 0.1% Triton-X suggests that this activity is accounted for by SPHK2. RT-PCR and in situ hybridization studies show that mRNA for this isoform has a distribution similar to that of SPHK activity. In vivo and in vitro ischemia increase SPHK activity and SPHK2 mRNA levels. These results indicate that SPHK2 is the predominant S1P-synthesizing isoform in normal brain parenchyma. Its heterogeneous distribution, in particular laminar distribution in cortex, suggests a neuronal localization and a possible role in cortical and cerebellar functions, in normal as well as ischemic brain.

Original languageEnglish
Pages (from-to)509-517
Number of pages9
JournalJournal of Neurochemistry
Volume103
Issue number2
DOIs
Publication statusPublished - Oct 2007
Externally publishedYes

Keywords

  • Cerebral ischemia
  • Glial cells
  • Neurons
  • Sphingolipid metabolism
  • Sphingosine-1-phosphate

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