Melanosome-iron interactions within retinal pigment epithelium-derived cells

Pigment Cell Melanoma Res. 2012 Nov;25(6):804-14. doi: 10.1111/pcmr.12008. Epub 2012 Oct 1.

Abstract

Melanosomes were recently shown to protect ARPE-19 cells, a human retinal pigment epithelium (RPE) cell line, against oxidative stress induced by hydrogen peroxide. One postulated mechanism of antioxidant action of melanin is its ability to bind metal ions. The aim here was to determine whether melanosomes are competent to bind iron within living cells, exhibiting a property previously shown only in model systems. The outcomes indicate retention of prebound iron and accumulation of iron by granules after iron delivery to cells via the culture medium, as determined by both colorimetric and electron spin resonance analyses for bound-to-melanosome iron. Manipulation of iron content did not affect the pigment's ability to protect cells against H(2) O(2) , but the function of pigment granules within RPE cells should be extended beyond a role in light irradiation to include participation in iron homeostasis.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoferritins / metabolism
  • Cell Line
  • Densitometry
  • Electron Spin Resonance Spectroscopy
  • Extracellular Space / drug effects
  • Extracellular Space / metabolism
  • Humans
  • Hydrogen Peroxide / pharmacology
  • Iron / metabolism*
  • Iron / pharmacology
  • Melanosomes / drug effects
  • Melanosomes / metabolism*
  • Microscopy, Phase-Contrast
  • Oxidative Stress / drug effects
  • Phagocytosis / drug effects
  • Retinal Pigment Epithelium / cytology*
  • Retinal Pigment Epithelium / drug effects
  • Retinal Pigment Epithelium / metabolism*
  • Sus scrofa

Substances

  • Apoferritins
  • Hydrogen Peroxide
  • Iron