Regulation of the on bipolar cell mGluR6 pathway by Ca2+

Scott Nawy

Research output: Contribution to journalArticle

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Abstract

Glutamate produces a hyperpolarizing synaptic potential in On bipolar cells by binding to the metabotropic glutamate receptor mGluR6, leading to closure of a cation channel. Here it is demonstrated that this cation channel is regulated by intracellular Ca2+. Glutamate-evoked currents were recorded from On bipolar cells in light-adapted salamander retinal slices in the presence of 2 mM external Ca2+. When glutamate was applied almost continuously interrupted only briefly to measure the size of the response, the glutamate response remained robust. However, currents elicited by intermittent and brief applications of glutamate exhibited time-dependent run down. Run down of the glutamate response was also voltage dependent, because it was accelerated by membrane hyperpolarization. Run down was triggered, at least in part, by a rise in intracelluar Ca2+ measured as a function of time or voltage, it was attenuated by intracellular buffering of Ca2+ with BAPTA or by omitting Ca2+ from the bathing solution. Current-voltage measurements demonstrated that Ca2+ induced run down of the glutamate response by downregulating cation channel function, rather than by preventing closure of the channel by glutamate and mGluR6. A major source of the Ca2+ that mediated this inhibition is the cation channel itself, which was found to be permeable to Ca2+, accounting for the use dependence of the run down. These results suggest that Ca2+ influx through the cation channel during background illumination could provide a signal to close the cation channel and repolarize the membrane toward its dark potential, an adaptive mechanism for coping with changes in ambient light.

Original languageEnglish (US)
Pages (from-to)4471-4479
Number of pages9
JournalJournal of Neuroscience
Volume20
Issue number12
Publication statusPublished - Jun 15 2000

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Keywords

  • Bipolar cell
  • Calcium
  • Cation channel
  • Metabotropic
  • Retina
  • mGluR6

ASJC Scopus subject areas

  • Neuroscience(all)

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