An increase of lysosomes through EGF-triggered endocytosis attenuated zinc-mediated lysosomal membrane permeabilization and neuronal cell death

Cell Death Dis. 2024 Nov 13;15(11):823. doi: 10.1038/s41419-024-07192-6.

Abstract

In the context of acute brain injuries, where zinc neurotoxicity and oxidative stress are acknowledged contributors to neuronal damage, we investigated the pivotal role of lysosomes as a potential protective mechanism. Our research commenced with an exploration of epidermal growth factor (EGF) and its impact on lysosomal dynamics, particularly its neuroprotective potential against zinc-induced cytotoxicity. Using primary mouse cerebrocortical cultures, we observed the rapid induction of EGFR endocytosis triggered by EGF, resulting in a transient increase in lysosomal vesicles. Furthermore, EGF stimulated lysosomal biogenesis, evident through elevated expression of lysosomal-associated membrane protein 1 (LAMP-1) and the induction and activation of prominent lysosomal proteases, particularly cathepsin B (CTSB). This process of EGFR endocytosis was found to promote lysosomal augmentation, thus conferring protection against zinc-induced lysosomal membrane permeabilization (LMP) and subsequent neuronal death. Notably, the neuroprotective effects and lysosomal enhancement induced by EGF were almost completely reversed by the inhibition of clathrin-mediated and caveolin-mediated endocytosis pathways, along with the disruption of retrograde trafficking. Furthermore, tyrosine kinase inhibition of EGFR nullified EGFR endocytosis, resulting in the abrogation of EGF-induced lysosomal upregulation and neuroprotection. An intriguing aspect of our study is the successful replication of EGF's neuroprotective effects through the overexpression of LAMP-1, which significantly reduced zinc-induced LMP and cell death, demonstrated in both primary mouse cerebrocortical neuronal cultures and human embryonic kidney (HEK) cells. Our research extended beyond zinc-induced neurotoxicity, as we observed EGF's protective effects against other oxidative stressors linked to intracellular zinc release, including hydrogen peroxide (H2O2) and 1-methyl-4-phenylpyridinium ion (MPP+). Collectively, our findings unveil the intricate interplay between EGF-triggered EGFR endocytosis, lysosomal upregulation, an increase in the regulatory capacity for zinc homeostasis, and the subsequent alleviation of zinc-induced neurotoxicity. These results present promising avenues for therapeutic interventions to enhance neuroprotection by targeting lysosomal augmentation.

MeSH terms

  • Animals
  • Cathepsin B / metabolism
  • Cell Death / drug effects
  • Cells, Cultured
  • Endocytosis* / drug effects
  • Epidermal Growth Factor* / metabolism
  • Epidermal Growth Factor* / pharmacology
  • ErbB Receptors* / metabolism
  • Humans
  • Intracellular Membranes / drug effects
  • Intracellular Membranes / metabolism
  • Lysosomes* / drug effects
  • Lysosomes* / metabolism
  • Mice
  • Neurons* / drug effects
  • Neurons* / metabolism
  • Neuroprotective Agents / pharmacology
  • Permeability / drug effects
  • Zinc* / metabolism
  • Zinc* / pharmacology

Substances

  • Zinc
  • Epidermal Growth Factor
  • ErbB Receptors
  • Cathepsin B
  • Neuroprotective Agents