JAG1/Notch Pathway Inhibition Induces Ferroptosis and Promotes Cataractogenesis

Int J Mol Sci. 2025 Jan 1;26(1):307. doi: 10.3390/ijms26010307.

Abstract

Cataracts remain the leading cause of visual impairment worldwide, yet the underlying molecular mechanisms, particularly in age-related cataracts (ARCs), are not fully understood. The Notch signaling pathway, known for its critical role in various degenerative diseases, may also contribute to ARC pathogenesis, although its specific involvement is unclear. This study investigates the role of Notch signaling in regulating ferroptosis in lens epithelial cells (LECs) and its impact on ARC progression. RNA sequencing of anterior lens capsule samples from ARC patients revealed a significant downregulation of Notch signaling, coupled with an upregulation of ferroptosis-related genes. Notch1 expression decreased, while ferroptosis markers increased in an age-dependent manner. In vitro, upregulation of Notch signaling alleviated ferroptosis by decreasing ferritin heavy chain 1 (FTH1) and p53 levels while enhancing the expression of nuclear factor erythroid 2-related factor 2 (Nrf2), glutathione peroxidase 4 (GPX4), and solute carrier family 7 member 11 (SLC7A11). Conversely, inhibition of Notch signaling exacerbated ferroptosis, as evidenced by reduced Nrf2, GPX4, and SLC7A11 expression. These findings suggest that downregulation of Notch signaling promotes ferroptosis in LECs by impairing the Nrf2/GPX4 antioxidant pathway, thereby contributing to ARC development. This study offers new insights into ARC pathogenesis and highlights the Notch signaling pathway as a potential therapeutic target for preventing or mitigating ARC progression.

Keywords: Notch; age-related cataract; ferroptosis; lens epithelial cells.

MeSH terms

  • Aged
  • Amino Acid Transport System y+ / genetics
  • Amino Acid Transport System y+ / metabolism
  • Apoferritins / genetics
  • Apoferritins / metabolism
  • Cataract* / genetics
  • Cataract* / metabolism
  • Cataract* / pathology
  • Epithelial Cells / metabolism
  • Female
  • Ferroptosis* / drug effects
  • Ferroptosis* / genetics
  • Humans
  • Jagged-1 Protein* / genetics
  • Jagged-1 Protein* / metabolism
  • Lens, Crystalline / metabolism
  • Male
  • Middle Aged
  • NF-E2-Related Factor 2* / genetics
  • NF-E2-Related Factor 2* / metabolism
  • Phospholipid Hydroperoxide Glutathione Peroxidase* / genetics
  • Phospholipid Hydroperoxide Glutathione Peroxidase* / metabolism
  • Receptor, Notch1 / genetics
  • Receptor, Notch1 / metabolism
  • Receptors, Notch / metabolism
  • Signal Transduction*
  • Tumor Suppressor Protein p53 / metabolism

Substances

  • Jagged-1 Protein
  • NF-E2-Related Factor 2
  • JAG1 protein, human
  • Phospholipid Hydroperoxide Glutathione Peroxidase
  • NFE2L2 protein, human
  • Amino Acid Transport System y+
  • Receptor, Notch1
  • SLC7A11 protein, human
  • Tumor Suppressor Protein p53
  • NOTCH1 protein, human
  • Receptors, Notch
  • Apoferritins