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Grants > The Role of Glutaredoxin 2 (Grx2), a Mitochondrial Thiol Repair Enzyme, in Age-Related Macular Degeneration Updated On: Ene. 21, 2025
Macular Degeneration Research Grant

The Role of Glutaredoxin 2 (Grx2), a Mitochondrial Thiol Repair Enzyme, in Age-Related Macular Degeneration

Hongli Wu, PhD

Principal Investigator

Hongli Wu, PhD

University of North Texas Health Science Center

Fort Worth, TX, USA

About the Research Project

Program

Macular Degeneration Research

Award Type

Standard

Award Amount

$160,000

Active Dates

July 01, 2015 - June 30, 2018

Grant ID

M2015180

Acknowledgement

This grant is made possible in part by a bequest from the Stuart Blydenburgh Trust.

Goals

Too many free radicals (bad molecules created by oxidation) in the retina are believed to cause age-related macular degeneration (AMD). Glutaredoxin 2 (Grx2) is a newly discovered antioxidant enzyme, which can break down free radicals in the retina. In this project, we will study if and how Grx2 protects retinal pigment epithelial (RPE) cells against free radicals. Results from this study may lead to a better treatment for AMD.

Summary

Free radicals are molecules that have become chemically destabilized due to oxidation—a chemical result of different types of stress. Our bodies accumulate free radicals through age and harmful exposures, and over time, they can lead to cellular damage. In the retina, free radicals are believed to cause diseases associated with aging, including age-related macular degeneration (AMD). Thus, understanding the function of antioxidant enzymes in the retina is critical for developing new therapies for AMD.

Glutaredoxin 2 (Grx2) is a newly identified antioxidant enzyme. As a multifunctional enzyme, Grx2 plays multiple roles in the battle against free radicals. On one hand, Grx2 can fight as a soldier to directly scavenge the free radicals. On the other hand, Grx2 can also serve as an army surgeon to repair and heal oxidatively damaged proteins. These properties distinguish Grx2 from other antioxidant enzymes as an attractive target for AMD treatment. In this project, we will study if and how this widely known, but little-studied, enzyme protects retinal pigment epithelial (RPE) cells against oxidative damage. The overall success of this project may identify a new therapeutic target for AMD and other oxidation-induced vision diseases.