Absence of DJ-1 causes age-related retinal abnormalities in association with increased oxidative stress

Vera L Bonilha1, Brent A Bell2, Mary E Rayborn2

  • 1Department of Ophthalmology, Cleveland Clinic Lerner College of Medicine at Case Western Reserve University, Cleveland, OH 44195, USA; Department of Ophthalmic Research, Cole Eye Institute, Cleveland Clinic, Cleveland, OH 44195, USA.

Insights

The DJ-1 protein protects retinal cells from oxidative stress. DJ-1 knockout mice show progressive retinal degeneration and increased oxidative stress markers, highlighting DJ-1

Area of Science:

  • Ophthalmology
  • Neuroscience
  • Cell Biology

Background:

  • Oxidative stress contributes to retinal cell death and geographic atrophy.
  • Molecular mechanisms regulating retinal oxidative stress are poorly understood.
  • DJ-1 protein is implicated in cellular protection against oxidative stress.

Purpose of the Study:

  • To investigate the role of DJ-1 in retinal oxidative stress response.
  • To evaluate photoreceptor and retinal pigment epithelium (RPE) changes in DJ-1 knockout mice.

Main Methods:

  • Examined young and aged DJ-1 knockout (DJ-1 KO) and wild-type mice.
  • Utilized scanning laser ophthalmoscopy (SLO), optical coherence tomography (OCT), and electroretinography (ERG).
  • Performed histological analysis and Western blotting for oxidative stress markers (Nrf2, protein carbonyls, iNOS).

Main Results:

  • DJ-1 KO mice exhibited increased RPE fluorescence and photoreceptor degeneration.
  • ERG showed reduced sensitivity in older DJ-1 KO mice.
  • DJ-1 KO retinas had elevated oxidative stress markers and reduced Nrf2 activation.

Conclusions:

  • DJ-1 plays a critical role in protecting photoreceptors and RPE from oxidative damage.
  • DJ-1 deficiency leads to progressive retinal degeneration associated with aging.
  • DJ-1 is a key regulator of the retinal oxidative stress response.