The CD36 Ligand-Promoted Autophagy Protects Retinal Pigment Epithelial Cells from Oxidative Stress

Oxid Med Cell Longev. 2021 Mar 28:2021:6691402. doi: 10.1155/2021/6691402. eCollection 2021.

Abstract

The retinal pigment epithelium (RPE) performs many functions that maintain photoreceptor health. Oxidative damage to the RPE is a critical component in the pathogenesis of eye diseases such as age-related macular degeneration (AMD). Ligands of the cluster of differentiation 36 (CD36) have previously preserved photoreceptor integrity in mouse models of AMD. The cytoprotective effect of the CD36 ligand MPE-001 on RPE cells has now been elucidated employing a model of oxidative stress. Sodium iodate (NaIO3) induced formation of reactive oxygen species and apoptosis in human RPE cells, which were decreased by MPE-001 without affecting antioxidant enzyme transcription. Immunoblotting and immunostaining assays showed a restorative effect of MPE-001 on the autophagic flux disrupted by NaIO3, which was associated with an increase in syntaxin 17-positive mature autophagosomes. The cytoprotective effect of MPE-001 was completely abolished by the autophagy inhibitors wortmannin and bafilomycin A1. In conclusion, we report for the first time an autophagy-dependent protection of RPE cells from oxidative stress by a CD36 ligand.

MeSH terms

  • Autophagy / drug effects
  • CD36 Antigens / metabolism*
  • Cell Line
  • Humans
  • Iodates / pharmacology
  • Ligands
  • Molecular Targeted Therapy
  • Oligopeptides / chemistry
  • Oligopeptides / pharmacology*
  • Oxidative Stress / drug effects*
  • Reactive Oxygen Species / metabolism
  • Retinal Pigment Epithelium / drug effects
  • Retinal Pigment Epithelium / metabolism*

Substances

  • CD36 Antigens
  • CD36 protein, human
  • Iodates
  • Ligands
  • Oligopeptides
  • Reactive Oxygen Species
  • growth hormone releasing hexapeptide
  • sodium iodate