Antioxidants in the prevention of UVB-induced keratynocyte apoptosis

J Photochem Photobiol B. 2014 Dec:141:1-9. doi: 10.1016/j.jphotobiol.2014.09.004. Epub 2014 Sep 16.

Abstract

Skin cells can respond to UVB-induced damage by counteracting it through antioxidant activation and DNA repair mechanisms or, when damage is massive by undergoing programmed cell death. Antioxidant factors, and, in particular, food compounds, have attracted much interest because of their potential use in new protective strategies for degenerative skin disorders. Melatonin, creatine and hydroxytyrosol show a variety of pharmacological and clinical benefits including anti-oxidant and anti-inflammatory activities. Here, the potential protective actions of antioxidant compounds against UVB-induced apoptosis were investigated in human keratinocytes. The cells were pre-treated with antioxidants before UVB exposure and their effect evaluated by means of ultrastructural and molecular analyses. After UVB radiation typical morphological apoptotic features and in situ DNA fragmentation after TUNEL reaction, appeared. A significant numerical decrease of apoptotic patterns could be observed when antioxidants were administrated before cell death induction. Moreover, both the intrinsic and extrinsic apoptotic pathways appeared activated after UVB radiation, and their down-regulation has been shown when antioxidants were added to cells before death induction. In conclusion, these compounds are able to prevent apoptotic cell death in human keratinocytes exposed to UVB, suggesting, for these molecules, an important role in preventing skin damage.

Keywords: Antioxidants; Apoptosis; Caspases; HaCaT; UVB; Ultrastructure.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antioxidants / pharmacology*
  • Apoptosis / drug effects*
  • Apoptosis / radiation effects
  • Caspases / metabolism
  • Cell Line
  • Creatine / pharmacology
  • DNA Fragmentation / drug effects
  • DNA Fragmentation / radiation effects
  • Humans
  • Intercellular Junctions / ultrastructure
  • Keratinocytes / cytology
  • Keratinocytes / metabolism
  • Melatonin / pharmacology
  • Microscopy, Fluorescence
  • Phenylethyl Alcohol / analogs & derivatives
  • Phenylethyl Alcohol / pharmacology
  • Poly(ADP-ribose) Polymerases / metabolism
  • Ultraviolet Rays*

Substances

  • Antioxidants
  • 3,4-dihydroxyphenylethanol
  • Poly(ADP-ribose) Polymerases
  • Caspases
  • Melatonin
  • Phenylethyl Alcohol
  • Creatine