CCL5-glutamate interaction in central nervous system: Early and acute presynaptic defects in EAE mice

Silvia Di Prisco, Elisa Merega, Marco Milanese, Maria Summa, Simona Casazza, Lizzia Raffaghello, Vito Pistoia, Antonio Uccelli, Anna Pittaluga

Research output: Contribution to journalArticlepeer-review

Abstract

We investigated the CCL5-glutamate interaction in the cortex and in the spinal cord from mice with Experimental Autoimmune Encephalomyelitis (EAE) at 13 and 21/30 days post immunization (d.p.i.), representing the onset and the peak of the disease, respectively. An early reduction of the KCl-evoked glutamate release was observed in cortical terminals from EAE mice at 13 d.p.i., persisting until 21/30 d.p.i. A concomitant reduction of the depolarization-evoked cyclic adenosine monophosphate (cAMP), but not of the inositol 1,4,5-trisphosphate (IP3) cortical production also occurred at 13 d.p.i, that still was detectable at the acute stage of disease (21 dp.i.). Inasmuch, the CCL5-mediated inhibition of glutamate exocytosis observed in control mice turned to facilitation in EAE mouse cortex at 13 d.p.i., then becoming undetectable at 21/30 d.p.i. Differently, glutamate exocytosis, as well as IP3 and cAMP productions were unaltered in spinal cord synaptosomes from EAE mice at 13 d.p.i., but significantly increased at 21/30 d.p.i., while the presynaptic CCL5-mediated facilitation of glutamate exocytosis observed in control mice remained unchanged. In both CNS regions, the presynaptic defects were parallelled by increased CCL5 availability. Inasmuch, the presynaptic defects so far described in EAE mice were reminiscent of the effects acute CCL5 exerts in control conditions. Based on these observations we propose that increased CCL5 bioavailability could have a role in determining the abovedescribed impaired presynaptic impairments in both CNS regions. These presynaptic defects could be relevant to the onset of early cognitive impairments and acute neuroinflammation and demyelinating processes observed in multiple sclerosis patients.

Original languageEnglish
Pages (from-to)337-346
Number of pages10
JournalNeuropharmacology
Volume75
DOIs
Publication statusPublished - 2013

Keywords

  • cAMP
  • CCL5
  • Cortex
  • EAE mice
  • Glutamate release
  • Spinal cord

ASJC Scopus subject areas

  • Cellular and Molecular Neuroscience
  • Pharmacology

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