Dependence of Reactive Oxygen Species and FLICE Inhibitory Protein on Lipofectamine-Induced Apoptosis in Human Lung Epithelial Cells

Details

• Personal Author:
  Azad N ; Iyer AKV ; Kongkaneramit L ; Lu Y ; Rojanasakul Y ; Sarisuta N ; Wang Y ; Azad N ; Iyer AKV ; Kongkaneramit L ; Lu Y ; Rojanasakul Y ; Sarisuta N ; Wang Y
• Description:
  Cationic liposomes such as Lipofectamine (LF) are widely used as nonviral gene delivery vectors; however, their clinical application is limited by their cytotoxicity. These agents have been shown to induce apoptosis as the primary mode of cell death, but their mechanism of action is not well understood. The present study investigated the mechanism of LF-induced apoptosis and examined the role of reactive oxygen species (ROS) in this process. We found that LF induced apoptosis of human epithelial H460 cells through a mechanism that involves caspase activation and ROS generation. Inhibition of caspase activity by pan-caspase inhibitor (z-VAD-fmk) or by specific caspase-8 inhibitor (z-IETD-fmk) or caspase-9 inhibitor (z-LEHD-fmk) inhibited the apoptotic effect of LF. Overexpression of FLICE-inhibitory protein (FLIP) or B-cell lymphoma-2, which are known inhibitors of the extrinsic and intrinsic death pathways, respectively, similarly inhibited apoptosis by LF. Induction of apoptosis by LF was shown to require ROS generation because its inhibition by ROS scavengers or by ectopic expression of antioxidant enzyme superoxide dismutase and glutathione peroxidase strongly inhibited the apoptotic effect of LF. Electron spin resonance studies showed that LF induced multiple ROS; however, superoxide was found to be the primary ROS responsible for LF-induced apoptosis. The mechanism by which ROS mediate the apoptotic effect of LF involves down-regulation of FLIP through the ubiquitination pathway. In demonstrating the role of FLIP and ROS in LF death signaling, we document a novel mechanism of apoptosis regulation that may be exploited to decrease cytotoxicity and increase gene transfection efficiency of cationic liposomes. [Description provided by NIOSH]
• Subjects:
  Antioxidants Cytotoxins Genetics Occupational Health Safety
• Keywords:
  Antioxidation Cytotoxic-effects Genes Pharmacology Therapeutic-agents
• ISSN:
  0022-3565
• Document Type:
  Text
• Genre:
  Journal Article ; Journal Article
• Place as Subject:
  OSHA Region 3 ; West Virginia
• CIO:
  National Institute for Occupational Safety and Health (NIOSH) ; National Institute for Occupational Safety and Health (NIOSH)
• Division:
  HELD - Health Effects Laboratory Division ; HELD - Health Effects Laboratory Division
• Topic:
  Workplace Safety & Health ; Workplace Safety & Health
• Location:
  North America ; North America
• Volume:
  325
• Issue:
  3
• NIOSHTIC Number:
  nn:20033880
• Citation:
  J Pharmacol Exp Ther 2008 Jun; 325(3):969-977
• Contact Point Address:
  Dr. Yon Rojanasakul, West Virginia University, Health Sciences Center, Department of Pharmaceutical Sciences, P.O. Box 9530, Morgantown, WV 26506
• Email:
  yrojan@hsc.wvu.edu
• Federal Fiscal Year:
  2008
• NORA Priority Area:
  Manufacturing ; Manufacturing
• Peer Reviewed:
  True
• Source Full Name:
  Journal of Pharmacology and Experimental Therapeutics
• Collection(s):
  National Institute for Occupational Safety and Health
• Main Document Checksum:
  urn:sha-512:e38a6141665d9108eef03ad60d85e9099ca3cb17507e7899f5d16d48ab83191ccb9bc361582bb70f6b436818c58bcf8b81278853b6abdd343de3026bbf129079
• Download URL:
  https://stacks.cdc.gov/view/cdc/189291/cdc_189291_DS1.pdf
• File Type:
  [PDF - 429.10 KB ]