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Grants > A Novel Model for Replacing Lost Cells and Restoring Vision in Glaucoma Patients Updated On: Ene. 21, 2025
National Glaucoma Research Grant

A Novel Model for Replacing Lost Cells and Restoring Vision in Glaucoma Patients

Protecting & Regenerating the Optic Nerve
Jeff Mumm, PhD

Principal Investigator

Jeffrey Mumm, PhD

Wilmer Eye Institute

Baltimore, MD, USA

About the Research Project

Program

National Glaucoma Research

Award Type

Standard

Award Amount

$180,000

Active Dates

September 01, 2020 - February 28, 2023

Grant ID

G2020315

Goals

To restore visual function to glaucoma patients, therapies are needed that can replace the specific cell types in the eye that are lost, retinal ganglion cells (RGCs). Although humans do not normally regenerate lost RGCs, our eyes do retain a capacity to produce new neurons, suggesting an untapped potential for RGC regeneration. Unlike us, zebrafish have a natural ability to replace lost cells in the retina, including RGCs. By studying how zebrafish are able to naturally regenerate lost RGCs, we hope to 1) identify genes and pathways that are important for stimulating the eyes ability to repair itself and 2) apply this knowledge toward the development of transformative regenerative therapies for glaucoma patients.

Summary

Our project has two goals: 1) to identify genes required to regenerate the retinal cell type lost in glaucoma patients, “retinal ganglion cells” (RGCs), and 2) to establish new models for studying how specific subtypes of RGCs can be regenerated. To restore visual function to persons suffering with glaucoma, therapies are needed to replace lost RGCs. Although humans do not normally regenerate lost RGCs, our eyes do appear to retain a capacity to produce new neurons, suggesting an untapped potential for RGC regeneration. Unlike us, fish have a natural ability to replace lost retinal cells, including RGCs. In Aim 1, we will use a novel fish model of glaucoma and a large-scale genetic testing approach to identify genes that are required to regenerate RGCs, thus, to reveal strategies for promoting the eyes ability to repair itself. Recent evidence has emerged that specific subtypes of RGCs may be lost in glaucoma patients, necessitating studies into how discrete RGC subtypes can be replaced. In Aim 2, we will create novel fish models that enable, for the first time, exploration of mechanisms that regulate the replacement of specific RGC subtypes. As very little is currently known about RGC regeneration, our research program is well positioned to advance new knowledge. It is our hope that insights generated from the proposed studies will support the development of transformative regenerative therapies for restoring lost visual function to glaucoma patients.