Molecular Brain (Oct 2012)

Protease activated receptor 1-induced glutamate release in cultured astrocytes is mediated by Bestrophin-1 channel but not by vesicular exocytosis

  • Oh Soo-Jin,
  • Han Kyung-Seok,
  • Park Hyungju,
  • Woo Dong ho,
  • Kim Hye,
  • Traynelis Stephen F,
  • Lee C

DOI
https://doi.org/10.1186/1756-6606-5-38
Journal volume & issue
Vol. 5, no. 1
p. 38

Abstract

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Abstract Background Glutamate is the major transmitter that mediates the principal form of excitatory synaptic transmission in the brain. It has been well established that glutamate is released via Ca2+-dependent exocytosis of glutamate-containing vesicles in neurons. However, whether astrocytes exocytose to release glutamate under physiological condition is still unclear. Findings We report a novel form of glutamate release in astrocytes via the recently characterized Ca2+-activated anion channel, Bestrophin-1 (Best1) by Ca2+ dependent mechanism through the channel pore. We demonstrate that upon activation of protease activated receptor 1 (PAR1), an increase in intracellular Ca2+ concentration leads to an opening of Best1 channels and subsequent release of glutamate in cultured astrocytes. Conclusions These results provide strong molecular evidence for potential astrocyte-neuron interaction via Best1-mediated glutamate release.

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