TNFα-induced apoptosis in human myeloid cell lines HL-60 and K562 is dependent of intracellular ROS generation

Mol Cell Biochem. 2014 May;390(1-2):281-7. doi: 10.1007/s11010-014-1979-5. Epub 2014 Feb 2.

Abstract

The present study determines the role of reactive oxygen species (ROS) production and calcium signaling evoked by the tumor necrosis factor-alpha (TNFα) on apoptosis in the human leukemia HL-60 and K562 cell lines. The results show that treatment of both cell lines cells with 10 ng/mL TNFα resulted in a rise in the percentage of apoptotic cells after 6 h of treatment. It was also observed that the administration of 10 ng/mL TNFα increased intracellular ROS production, as well as a time-dependent increase in caspase-8, -3, and -9 activities. The present results also show that the pretreatment with well-known antioxidants such as trolox and N-acetyl cysteine partially reduced the caspase activation caused by the administration of TNFα. The findings suggest that TNFα-induced apoptosis is dependent on alterations in intracellular ROS generation in human leukemia HL-60 and K562 cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / drug effects
  • Apoptosis / genetics*
  • Caspase Inhibitors / administration & dosage
  • Caspases / biosynthesis*
  • Chromans / administration & dosage
  • Gene Expression Regulation, Neoplastic / drug effects
  • HL-60 Cells
  • Humans
  • K562 Cells
  • Leukemia / genetics*
  • Leukemia / metabolism
  • Leukemia / pathology
  • Reactive Oxygen Species / metabolism
  • Tumor Necrosis Factor-alpha / administration & dosage*
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Caspase Inhibitors
  • Chromans
  • Reactive Oxygen Species
  • Tumor Necrosis Factor-alpha
  • Caspases
  • 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid