The inhibitory input to mouse cerebellar Purkinje cells is reciprocally modulated by Bergmann glial P2Y1 and AMPA receptor signaling

Ramona Rudolph, Hannah M. Jahn, Raphael Jean Courjaret, Nanette Messemer, Frank Kirchhoff, Joachim W. Deitmer

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

Synaptic transmission has been shown to be modulated by glial functions, but the modes of specific glial action may vary in different neural circuits. We have tested the hypothesis, if Bergmann GLIA (BG) are involved in shaping neuronal communication in the mouse cerebellar cortex, using acutely isolated cerebellar slices of wild-type (WT) and of glia-specific receptor knockout mice. Activation of P2Y1 receptors by ADP (100 μM) or glutamatergic receptors by AMPA (0.3 μM) resulted in a robust, reversible and repeatable rise of evoked inhibitory input in Purkinje cells by 80% and 150%, respectively. The ADP-induced response was suppressed by prior application of AMPA, and the AMPA-induced response was suppressed by prior application of ADP. Genetic deletion or pharmacological blockade of either receptor restored the response to the other receptor agonist. Both ADP and AMPA responses were sensitive to Rose Bengal, which blocks vesicular glutamate uptake, and to the NMDA receptor antagonist D-AP5. Our results provide strong evidence that activation of both ADP and AMPA receptors, located on BGs, results in the release of glutamate, which in turn activates inhibitory interneurons via NMDA-type glutamate receptors. This infers that BG cells, by means of metabotropic signaling via their AMPA and P2Y1 receptors, which mutually suppress each other, would interdependently contribute to the fine-tuning of Purkinje cell activity in the cerebellar cortex.

Original languageEnglish
Pages (from-to)1265-1280
Number of pages16
JournalGLIA
Volume64
Issue number7
DOIs
Publication statusPublished - 1 Jul 2016
Externally publishedYes

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Keywords

  • ADP
  • Gliotransmission
  • Glutamate
  • NMDA receptors

ASJC Scopus subject areas

  • Neurology
  • Cellular and Molecular Neuroscience

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