Glutamate transporters are involved in direct inhibitory synaptic transmission in the vertebrate retina

Author:

Niklaus Stephanie1,Glasauer Stella M. K.1,Kovermann Peter2,Farshori Kulsum F.1,Cadetti Lucia1,Früh Simon1,Rieser Nicolas N.1,Gesemann Matthias1,Zang Jingjing1,Fahlke Christoph2,Neuhauss Stephan C. F.1ORCID

Affiliation:

1. Department of Molecular Life Sciences, University of Zurich, Winterthurerstrasse 190 , 8057 Zurich, Switzerland

2. Institute of Biological Information Processing, Molekular- und Zellphysiologie (IBI-1), Forschungszentrum Jülich, Leo-Brandt-Strasse , 52425 Jülich, Germany

Abstract

In the central nervous system of vertebrates, glutamate serves as the primary excitatory neurotransmitter. However, in the retina, glutamate released from photoreceptors causes hyperpolarization in post-synaptic ON-bipolar cells through a glutamate-gated chloride current, which seems paradoxical. Our research reveals that this current is modulated by two excitatory glutamate transporters, EAAT5b and EAAT7. In the zebrafish retina, these transporters are located at the dendritic tips of ON-bipolar cells and interact with all four types of cone photoreceptors. The absence of these transporters leads to a decrease in ON-bipolar cell responses, with eaat5b mutants being less severely affected than eaat5b / eaat7 double mutants, which also exhibit altered response kinetics. Biophysical investigations establish that EAAT7 is an active glutamate transporter with a predominant anion conductance. Our study is the first to demonstrate the direct involvement of post-synaptic glutamate transporters in inhibitory direct synaptic transmission at a central nervous system synapse.

Funder

Swiss National Science Foundation

Publisher

The Royal Society

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