Cyclo(phenylalanine-proline) induces DNA damage in mammalian cells via reactive oxygen species

J Cell Mol Med. 2015 Dec;19(12):2851-64. doi: 10.1111/jcmm.12678. Epub 2015 Sep 28.

Abstract

Cyclo(phenylalanine-proline) is produced by various organisms such as animals, plants, bacteria and fungi. It has diverse biological functions including anti-fungal activity, anti-bacterial activity and molecular signalling. However, a few studies have demonstrated the effect of cyclo(phenylalanine-proline) on the mammalian cellular processes, such as cell growth and apoptosis. In this study, we investigated whether cyclo(phenylalanine-proline) affects cellular responses associated with DNA damage in mammalian cells. We found that treatment of 1 mM cyclo(phenylalanine-proline) induces phosphorylation of H2AX (S139) through ATM-CHK2 activation as well as DNA double strand breaks. Gene expression analysis revealed that a subset of genes related to regulation of reactive oxygen species (ROS) scavenging and production is suppressed by the cyclo(phenylalanine-proline) treatment. We also found that cyclo(phenylalanine-proline) treatment induces perturbation of the mitochondrial membrane, resulting in increased ROS, especially superoxide, production. Collectively, our study suggests that cyclo(phenylalanine-proline) treatment induces DNA damage via elevation of ROS in mammalian cells. Our findings may help explain the mechanism underlying the bacterial infection-induced activation of DNA damage response in host mammalian cells.

Keywords: DNA damage; comet assay; cyclo dipeptide; cyclo(phenylalanine-proline); reactive oxygen species.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / drug effects
  • Apoptosis / genetics
  • Ataxia Telangiectasia Mutated Proteins / genetics
  • Ataxia Telangiectasia Mutated Proteins / metabolism
  • Blotting, Western
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Cell Proliferation / genetics
  • Checkpoint Kinase 2 / genetics
  • Checkpoint Kinase 2 / metabolism
  • DNA Breaks, Double-Stranded / drug effects*
  • Dipeptides / pharmacology*
  • Gene Expression / drug effects
  • Histones / metabolism
  • Humans
  • Membrane Potential, Mitochondrial / drug effects
  • Microscopy, Confocal
  • Peptides, Cyclic / pharmacology*
  • Phosphorylation / drug effects
  • RNA Interference
  • Reactive Oxygen Species / metabolism*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Superoxides / metabolism

Substances

  • Dipeptides
  • H2AX protein, human
  • Histones
  • Peptides, Cyclic
  • Reactive Oxygen Species
  • cyclo(phenylalanyl-prolyl)
  • Superoxides
  • Checkpoint Kinase 2
  • Ataxia Telangiectasia Mutated Proteins