Background glaucoma Shape Background glaucoma Shape Background glaucoma Shape
Grants > Using Electric Fields to Regenerate the Optic Nerve Updated On: Ene. 21, 2025
National Glaucoma Research Grant

Using Electric Fields to Regenerate the Optic Nerve

Protecting & Regenerating the Optic Nerve
Kimberly Gokoffski, MD, PhD

Principal Investigator

Kimberly Gokoffski, MD, PhD

University of Southern California

Los Angeles, CA, USA

About the Research Project

Program

National Glaucoma Research

Award Type

Standard

Award Amount

$190,000

Active Dates

September 01, 2020 - August 31, 2023

Grant ID

G2020331

Acknowledgement

Recipient of the Dr. Douglas H. Johnson Award for Glaucoma Research.

Goals

It is estimated that 18 million people worldwide are legally blind from glaucoma, a disease that damages the optic nerve, the cable that connects the eye to the brain. Blindness in patients with glaucoma is currently irreversible because the cells that make up the optic nerve, retinal neurons, are not able to regenerate. Although scientists have been able to use stem cells produce new healthy neurons, when these neurons are injected into the eye, they are unable to form new connections with the brain. This project employs an innovative technology that uses electrical stimulation to direct neuron growth so that healthy neurons that have been injected into diseased eyes may form new connections with the brain and thereby restore vision.

Summary

The goal of our research is to develop a technology to help damaged retinal ganglion cells (RGCs) regrow their long tails (axons) and re-establish connections with the brain. In glaucoma, RGCs sustain damage to their axons which causes them to retract and eventually leads to degeneration of the neuron itself. Technologies that can 1) direct native RGCs to regrow their axons and/or 2) direct the formation and growth of axons in transplanted RGCs are needed to restore vision in patients blinded by glaucoma. Building on our previous work, we will transform electric field application into a viable technology to direct regrowth of injured RGC axons. We have previously shown that electric fields (EFs) promote retinal ganglion cell (RGC) axon growth in tissue culture. Here, we plan to translate our previous work and develop EF application as a breakthrough therapy to regenerate RGC axons in vivo. In addition, we propose to use genetic approaches to manipulate RGC cellular machinery and evaluate potential synergistic effects on promoting axon regeneration when applied in conjunction with EFs. This technology would be the first device shown to be effective at regenerating the optic nerve after it has been damaged. Once completed, this work will be pivotal in propelling the development of a device that can help restore vision in patients blinded by advanced glaucoma.