# The role of electrical synaptic plasticity in retinal function

> **NIH NIH R21** · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · 2020 · $183,802

## Abstract

Project Summary
 Neurons of the central nervous system are organized into networks through a variety of synaptic
interactions. Electrical synapses, formed by gap junctions between neurons, are a core component of this
organization. Electrical synapses can synchronize activity of networks of the same neuron type and provide
rapid, bi-directional electrical communication between neurons of different type. These properties are critical
for many high-order network functions of the central nervous system.
 Electrical synapses are not static, but are tightly regulated. Changes in phosphorylation state of connexin
36 (Cx36) in some retinal neurons modify coupling quantitatively over more than an order of magnitude
dynamic range. Such changes in coupling are a stereotyped element of retinal light adaptation, and many
electrically coupled retinal networks are held in a very poorly coupled state during the daytime to optimize their
function. The vast majority of electrical synapses throughout the central nervous system are composed of
Cx36. ALL of these synapses are capable of the same scale of plasticity, but very little is known about the
plasticity of most networks or their functional state.
 This project explores the hypothesis that optimal function of electrically coupled networks is often best
served by weak coupling. To test this hypothesis we will develop conditional mutant mice in which the
electrical synapses are locked in an open state by point mutations that mimic phosphorylation of Cx36. This
should cause unusually high coupling in most networks affected. These animals will be used to determine the
impact of strong coupling of neural networks in the retina in the daytime on visual functions and behavior.
Further studies will examine specifically the necessity to use electrical synaptic plasticity to reconfigure rod
visual pathways in the daytime to optimize ganglion cell responses in photopic light. This animal model will be
useful to study plasticity of electrical coupling in most other circuits in the central nervous system. It will have
further utility in studies of the role of gap junctional coupling in bystander cell death in brain injuries and
diseases.

## Key facts

- **NIH application ID:** 10064771
- **Project number:** 3R21EY027965-02S1
- **Recipient organization:** UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON
- **Principal Investigator:** JOHN O'BRIEN
- **Activity code:** R21 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2020
- **Award amount:** $183,802
- **Award type:** 3
- **Project period:** 2020-02-01 → 2021-01-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10064771

## Citation

> US National Institutes of Health, RePORTER application 10064771, The role of electrical synaptic plasticity in retinal function (3R21EY027965-02S1). Retrieved via AI Analytics 2026-05-22 from https://api.ai-analytics.org/grant/nih/10064771. Licensed CC0.

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