4.5 Article

Iron upregulates melanogenesis in cultured retinal pigment epithelial cells

Journal

EXPERIMENTAL EYE RESEARCH
Volume 128, Issue -, Pages 92-101

Publisher

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.exer.2014.09.010

Keywords

Iron; Retinal pigment epithelium; Human fetal retinal pigment epithelial cells; ARPE-19 cells; Melanosome; MITF; LEF 1

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Funding

  1. NIH/NEI [R01 EY015240]
  2. FM Kirby Foundation
  3. Research to Prevent Blindness
  4. Paul and Evanina Bell MacKall Foundation Trust

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The purpose of our studies was to examine the relationship between iron and melanogenesis in retinal pigment epithelial cells, as prior observations had suggested that iron may promote melanogenesis. This relationship has potential clinical importance, as both iron overload and hyperpigmentation are associated with age-related macular degeneration (AMD). Human fetal retinal pigment epithelial cells and ARPE-19 cells were treated with iron in the form of ferric ammonium citrate, after which quantitative RTPCR and electron microscopy were performed. Melanogenesis genes tyrosinase, tyrosinase-related protein 1, Hermansky-Pudlak Syndrome 3, premelanosome protein and dopachrome tautomerase were upregulated, as was the melanogenesis-controlling transcription factor, microphthalmia-associated transcription factor (MITF). Iron-treated cells had increased pigmentation and melanosome number. Multiple transcription factors upstream of MITF were upregulated by iron. (C) 2014 Elsevier Ltd. All rights reserved.

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