Glutamate release from astrocytes is stimulated via the appearance of exocytosis during cyclic AMP-induced morphologic changes

Hatsuki Shiga, Jun Murakami, Takashi Nagao, Motoki Tanaka, Koichi Kawahara, Ichiro Matsuoka, Etsuro Ito

Research output: Contribution to journalArticle

10 Citations (Scopus)

Abstract

Recent studies have shown that astrocytes release various transmitters including glutamate and thus directly affect synaptic neurotransmission. The mechanisms involved in the release of glutamate from astrocytes remain unclear, however. In the present study, we examined differences in 1) the amount of glutamate released, 2) the appearance of exocytosis, and 3) the expression of SNARE (soluble N-ethylmaleimide sensitive fusion protein attachment protein receptor) proteins between cyclic AMP-treated and non-treated astrocytes in culture. Extracellular glutamate was detected in the recording solution of cyclic AMP-treated astrocytes after stimulation with ATP by high-performance liquid chromatography and NADH imaging. Exocytosis, which was observed by FM1-43 imaging, appeared in cyclic AMP-treated astrocytes in a punctiform fashion, but not in non-treated cells, after stimulation with ATP and glutamate. Immunocytochemistry and Western blotting showed that the amount of SNARE proteins increased during cAMP-induced morphologic changes, and in particular, a v-SNARE, synaptobrevin, appeared as punctiform staining in the cytosol of cyclic AMP-treated astrocytes. These findings show that astrocytes acquire SNARE proteins during cyclic AMP-induced differentiation, and suggest that glutamate is released by exocytosis in cyclic AMP-treated astrocytes in response to ATP released from neighboring neurons and astrocytes.

Original languageEnglish
Pages (from-to)338-347
Number of pages10
JournalJournal of Neuroscience Research
Volume84
Issue number2
DOIs
Publication statusPublished - 2006 Aug 1

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Keywords

  • ATP
  • FM1-43 imaging
  • Gliotransmitter
  • HPLC
  • NADH imaging
  • SNARE protein

ASJC Scopus subject areas

  • Cellular and Molecular Neuroscience

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