Cysteinyl leukotriene receptor 1 modulates autophagic activity in retinal pigment epithelial cells

Sci Rep. 2020 Oct 19;10(1):17659. doi: 10.1038/s41598-020-74755-w.

Abstract

The retinal pigment epithelium (RPE), which is among the tissues in the body that are exposed to the highest levels of phagocytosis and oxidative stress, is dependent on autophagy function. Impaired autophagy and continuous cellular stress are associated with various disorders, such as dry age-related macular degeneration (AMD), a disease for which effective therapies are lacking. Cysteinyl leukotriene receptor (CysLTR) 1 is a potential modulator of autophagy; thus, the aim of this study was to investigate the role of CysLTR1 in autophagy regulation in the RPE cell line ARPE-19. The polarized ARPE-19 monolayer exhibited expression of CysLTR1, which was colocalized with β-tubulin III. In ARPE-19 cells, autophagic activity was rhythmically regulated and was increased upon CysLTR1 inhibition by Zafirlukast (ZK) treatment. H2O2 affected the proautophagic regulatory effect of ZK treatment depending on whether it was applied simultaneously with or prior to ZK treatment. Furthermore, mRNA levels of genes related to the leukotriene system, autophagy and the unfolded protein response were positively correlated. As CysLTR1 is involved in autophagy regulation under basal and oxidative stress conditions, a dysfunctional leukotriene system could negatively affect RPE functions. Therefore, CysLTR1 is a potential target for new treatment approaches for neurodegenerative disorders, such as AMD.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Autophagy*
  • Cell Line
  • Fluorescent Antibody Technique
  • Gene Expression Regulation
  • Humans
  • Hydrogen Peroxide / metabolism
  • Indoles
  • Leukotriene Antagonists / pharmacology
  • Oxidative Stress
  • Phenylcarbamates
  • Polymerase Chain Reaction
  • Receptors, Leukotriene / drug effects
  • Receptors, Leukotriene / metabolism*
  • Receptors, Leukotriene / physiology
  • Retinal Pigment Epithelium / cytology
  • Retinal Pigment Epithelium / metabolism*
  • Retinal Pigment Epithelium / physiology
  • Sulfonamides
  • Tosyl Compounds / pharmacology
  • Transcription Factors / metabolism

Substances

  • Indoles
  • Leukotriene Antagonists
  • Phenylcarbamates
  • Receptors, Leukotriene
  • Sulfonamides
  • Tosyl Compounds
  • Transcription Factors
  • Hydrogen Peroxide
  • leukotriene D4 receptor
  • zafirlukast