Skip to main navigation Skip to search Skip to main content

Long-term plasticity mediated by mGluR1 at a retinal reciprocal synapse

Research output: Contribution to journalArticlepeer-review

Abstract

The flow of information across the retina is controlled by reciprocal synapses between bipolar cell terminals and amacrine cells. However, the synaptic delays and properties of plasticity at these synapses are not known. Here we report that glutamate release from goldfish Mb-type bipolar cell terminals can trigger fast (delay of 2-3 ms) and transient GABAA IPSCs and a much slower and more sustained GABAC feedback. Synaptically released glutamate activated mGluR1 receptors on amacrine cells and, depending on the strength of presynaptic activity, potentiated subsequent feedback. This poststimulus enhancement of GABAergic feedback lasted for up to 10 min. This form of mGluR1-mediated long-term synaptic plasticity may provide retinal reciprocal synapses with adaptive capabilities.

Original languageEnglish (US)
Pages (from-to)469-482
Number of pages14
JournalNeuron
Volume46
Issue number3
DOIs
StatePublished - May 5 2005

Funding

We thank Dr. Paul Witkovsky, New York University Medical Center, and Dr. Ko Matsui, Vollum Institute, for critically reading and commenting on the manuscript. This research was supported by HFSP and NIH-NEI grants.

FundersFunder number
NIH-NEI
National Institute of Neurological Disorders and StrokeF31NS042506
Horowitz Foundation for Social Policy

    ASJC Scopus subject areas

    • General Neuroscience

    Fingerprint

    Dive into the research topics of 'Long-term plasticity mediated by mGluR1 at a retinal reciprocal synapse'. Together they form a unique fingerprint.

    Cite this