1. Academic Validation
  2. Lysosome dysfunction enhances oxidative stress-induced apoptosis through ubiquitinated protein accumulation in Hela cells

Lysosome dysfunction enhances oxidative stress-induced apoptosis through ubiquitinated protein accumulation in Hela cells

  • Anat Rec (Hoboken). 2013 Jan;296(1):31-9. doi: 10.1002/ar.22612.
Chunyan Yu 1 Xiaowei Huang Ye Xu Hongyan Li Jing Su Jiateng Zhong Jinsong Kang Yuhe Liu Liankun Sun
Affiliations

Affiliation

  • 1 Department of Pathophysiology, Norman Bethune College of Medicine, Jilin University, Changchun, China.
Abstract

The role of lysosomal system in oxidative stress-induced Apoptosis in Cancer cells is not fully understood. Menadione is frequently used as oxidative stress model. It is indicated that menadione could induce Autophagy in Hela cells. In the present study, we examined whether the lysosomal inhibitor, ammonium chloride (NH(4)Cl) could prevent the Autophagy flux by inhibiting the fusion of autophagosomes with lysosomes and enhance Apoptosis induced by menadione via mitochondrial pathway. The results demonstrated generation and accumulation of Reactive Oxygen Species and increased levels of ubiquitinated proteins and GRP78 in cells treated with both menadione and NH(4)Cl. Our data indicates that lysosomal system through Autophagy plays an important role in preventing menadione-induced Apoptosis in Hela cells by clearing misfolded proteins, which alleviates endoplasmic reticulum stress.

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