GABAA presynaptic inhibition regulates the gain and kinetics of retinal output neurons

Author:

Nagy Jenna123,Ebbinghaus Briana245,Hoon Mrinalini124,Sinha Raunak124ORCID

Affiliation:

1. Department of Neuroscience, University of Wisconsin, Madison, United States

2. McPherson Eye Research Institute, University of Wisconsin, Madison, United States

3. Cellular and Molecular Pathology Training Program, University of Wisconsin, Madison, United States

4. Department of Ophthalmology and Visual Sciences, University of Wisconsin, Madison, United States

5. Neuroscience Training Program, University of Wisconsin, Madison, United States

Abstract

Output signals of neural circuits, including the retina, are shaped by a combination of excitatory and inhibitory signals. Inhibitory signals can act presynaptically on axon terminals to control neurotransmitter release and regulate circuit function. However, it has been difficult to study the role of presynaptic inhibition in most neural circuits due to lack of cell type-specific and receptor type-specific perturbations. In this study, we used a transgenic approach to selectively eliminate GABAA inhibitory receptors from select types of second-order neurons – bipolar cells – in mouse retina and examined how this affects the light response properties of the well-characterized ON alpha ganglion cell retinal circuit. Selective loss of GABAA receptor-mediated presynaptic inhibition causes an enhanced sensitivity and slower kinetics of light-evoked responses from ON alpha ganglion cells thus highlighting the role of presynaptic inhibition in gain control and temporal filtering of sensory signals in a key neural circuit in the mammalian retina.

Funder

National Eye Institute

University of Wisconsin-Madison

Research to Prevent Blindness

National Institute of General Medical Sciences

National Institute of Neurological Disorders and Stroke

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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