# Regulation of Retinal Gap Junctions

> **NIH NIH R01** · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · 2021 · $442,068

## Abstract

Synaptic communication in the nervous system is accomplished by two major classes of synapses, chemical
and electrical, which operate in different ways. Electrical synapses are formed by gap junctions between neurons
and allow passage of electrical current directly between cells, providing fast and often bi-directional
communication. Cellular control of the magnitude of this communication refines local and long-range neural
network functions, and is an important component of network plasticity. Electrical synapse plasticity plays a
particularly important role in sensory adaptation in the vertebrate retina, where changes in coupling of some
networks exceed an order of magnitude.
 The long-term goals of this established research project are to elucidate the mechanisms that control
plasticity of electrical synapses. In recent work, we have discovered an intimate relationship between the actin
cytoskeleton and functional control of coupling in Connexin 36 (Cx36) gap junctions. This appears to integrate
the main components of excitatory and inhibitory signaling and switching between those modes. This project
will investigate those links, using a combination of cell culture and mouse retina model systems. We will test
three specific hypotheses about regulation of Cx36 functional coupling in the following ways: (1) Signaling protein
complexes that regulate Cx36 coupling are associated with the actin cytoskeleton. Using proximity labeling and
quantitative proteomic techniques, we will identify signaling components involved in the regulation of Cx36
coupling. We will further investigate the dynamic changes in proximity of these components to Cx36 during
regulatory signaling. (2) Phosphorylation of Cx36 alters its association with signaling components. We will
investigate how phosphorylation of certain residues of Cx36 regulates the association of some signaling
components. (3) RhoA and Cdc42 signaling pathways modulate functional plasticity. We will investigate how
pathways that control cytoskeletal remodeling influence coupling of Cx36.
 The proposed studies will elucidate mechanisms central to control of electrical synapse functional plasticity.
Knowledge of these mechanisms will provide a great deal of insight not only into the control of visual adaptation
processes in the retina, but also electrical synapse plasticity throughout the brain. This will allow the
development of targeted therapies for disorders in which gap junctions play a role.

## Key facts

- **NIH application ID:** 10120785
- **Project number:** 2R01EY012857-17A1
- **Recipient organization:** UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON
- **Principal Investigator:** JOHN O'BRIEN
- **Activity code:** R01 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2021
- **Award amount:** $442,068
- **Award type:** 2
- **Project period:** 2000-02-01 → 2021-09-01

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10120785

## Citation

> US National Institutes of Health, RePORTER application 10120785, Regulation of Retinal Gap Junctions (2R01EY012857-17A1). Retrieved via AI Analytics 2026-05-25 from https://api.ai-analytics.org/grant/nih/10120785. Licensed CC0.

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