Lysosomal membrane permeabilization contributes to elemene emulsion-induced apoptosis in A549 cells

Free Radic Res. 2011 Oct;45(10):1232-40. doi: 10.3109/10715762.2011.607818. Epub 2011 Aug 17.

Abstract

Elemene is a broad-spectrum antitumor agent. In the present study, lysosomal membrane permeabilization (LMP) was detected after short elemene emulsion--exposure (12 h) that preceded a decrease of the mitochondrial membrane potential and DNA damage (24 h) in A549 cells. At later time points (36 h) elemene emulsion caused the appearance of A549 cells with apoptotic features, including apoptotic morphology, phosphatidylserine exposure, and caspase-3 activation. A significant increase in protein expression for cathepsin D was also observed utilizing Western blot analysis after exposure to elemene emulsion for 12 h. The present study showed that elemene emulsion induced the increased levels of reactive oxygen species (ROS) and depletion of glutathione (GSH) in A549 cells. Cells treated with pepstatin A, an inhibitor for cathepsin D, showed a significant inhibition in DNA damage, mitochondrial membrane permeabilization, caspase-3 activation, and phosphatidylserine exposure. These results demonstrated that apoptosis induced by elemene emulsion in A549 cells is mediated in part through LMP and lysosomal protease cathepsin D.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma / drug therapy*
  • Adenocarcinoma / metabolism
  • Adenocarcinoma / pathology
  • Adenocarcinoma of Lung
  • Antineoplastic Agents / pharmacokinetics
  • Antineoplastic Agents / pharmacology
  • Apoptosis / drug effects*
  • Caspase 3 / metabolism
  • Cathepsin D / antagonists & inhibitors
  • Cathepsin D / metabolism
  • Cell Line, Tumor
  • Cell Membrane Permeability / drug effects
  • Cell Membrane Permeability / physiology
  • Glutathione / metabolism
  • Humans
  • Intracellular Membranes / drug effects
  • Intracellular Membranes / metabolism*
  • Lung Neoplasms / drug therapy*
  • Lung Neoplasms / metabolism
  • Lung Neoplasms / pathology
  • Lysosomes / drug effects
  • Lysosomes / metabolism*
  • Membrane Potential, Mitochondrial / drug effects
  • Membrane Potential, Mitochondrial / physiology
  • Mitochondria / drug effects
  • Mitochondria / metabolism
  • Pepstatins / pharmacology
  • Reactive Oxygen Species / metabolism
  • Sesquiterpenes / pharmacokinetics*
  • Sesquiterpenes / pharmacology

Substances

  • Antineoplastic Agents
  • Pepstatins
  • Reactive Oxygen Species
  • Sesquiterpenes
  • elemene
  • Caspase 3
  • CTSD protein, human
  • Cathepsin D
  • Glutathione
  • pepstatin