Melanosome-iron interactions within retinal pigment epithelium-derived cells

被引:29
|
作者
Kaczara, Patrycja [2 ]
Zareba, Mariusz [1 ]
Herrnreiter, Anja [1 ]
Skumatz, Christine M. B. [1 ]
Zadlo, Andrzej [2 ]
Sarna, Tadeusz [2 ]
Burke, Janice M. [1 ]
机构
[1] Med Coll Wisconsin, Dept Ophthalmol, Milwaukee, WI 53226 USA
[2] Jagiellonian Univ, Dept Biophys, Fac Biochem Biophys & Biotechnol, PL-30387 Krakow, Poland
关键词
melanin; melanosomes; iron; retinal pigment epithelium; oxidative stress; aging; hydrogen peroxide; ELECTRON-SPIN RESONANCE; HUMAN RPE MELANOSOMES; MACULAR DEGENERATION; HYDROGEN-PEROXIDE; OXIDATIVE DAMAGE; PHOTIC STRESS; HYDROXYL RADICALS; SYNTHETIC DOPA; MELANIN; NEUROMELANIN;
D O I
10.1111/pcmr.12008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 H2O2, but the function of pigment granules within RPE cells should be extended beyond a role in light irradiation to include participation in iron homeostasis.
引用
收藏
页码:804 / 814
页数:11
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