The Potential Role of Regulated Cell Death in Dry Eye Diseases and Ocular Surface Dysfunction

Camilla Scarpellini1, Alba Ramos Llorca1, Caroline Lanthier1

  • 1Laboratory of Medicinal Chemistry, University of Antwerp, Universiteitsplein 1, B-2160 Antwerp, Belgium.

Insights

New research explores regulated cell death (RCD) mechanisms like ferroptosis, necroptosis, and pyroptosis as novel therapeutic targets for dry eye disease (DED). Understanding these pathways could lead to better treatments for this growing condition.

Area of Science:

  • Ophthalmology
  • Cell Biology
  • Pathology

Background:

  • Dry eye disease (DED) prevalence is increasing, especially in younger populations, necessitating novel therapeutic targets.
  • Regulated cell death (RCD) is crucial for tissue homeostasis, with various mechanisms implicated in human pathologies.
  • While apoptosis is studied in DED, other RCD types require further elucidation in ocular surface dysfunction.

Purpose of the Study:

  • To review the potential roles of different regulated cell death (RCD) mechanisms in dry eye disease (DED).
  • To explore novel therapeutic targets for DED based on RCD pathways.
  • To analyze the therapeutic applications of ferroptosis, necroptosis, and pyroptosis in DED.

Main Methods:

  • Literature review focusing on RCD mechanisms in DED.
  • Analysis of existing evidence on oxidative stress and inflammation in DED.
  • Exploration of ferroptosis, necroptosis, and pyroptosis in the context of ocular surface disease.

Main Results:

  • Oxidative stress and inflammation are key features of dry eye pathology.
  • Ferroptosis, necroptosis, and pyroptosis represent potential therapeutic avenues for DED.
  • Further research is needed to fully understand the role of RCD in DED pathogenesis.

Conclusions:

  • Regulated cell death (RCD) pathways beyond apoptosis hold significant promise for DED treatment.
  • Targeting RCD mechanisms could offer innovative therapeutic strategies for dry eye disease.
  • Elucidating the specific roles of ferroptosis, necroptosis, and pyroptosis is critical for advancing DED therapy.

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