Ferroxidase Hephaestin's Cell-Autonomous Role in the Retinal Pigment Epithelium

Abstract

Hephaestin (Heph) is a ferroxidase protein that converts ferrous to ferric iron to facilitate cellular iron export by ferroportin. Many tissues express either Heph or its homologue, ceruloplasmin (Cp), but the retina expresses both. In mice, a combined systemic mutation of Heph and systemic knockout of Cp (Cp(-/-), Heph(sla/sla)) causes retinal iron accumulation and retinal degeneration, with features of human age-related macular degeneration; however, the role of Heph and Cp in the individual retinal cells is unclear. Herein, we used conditional knockout mice to study Heph's role in retinal pigment epithelial (RPE) and photoreceptor cells. Loss of both Heph and Cp from RPE cells alone results in RPE cell iron accumulation and degeneration. We found, however, that RPE iron accumulation in these conditional knockout mice is not as great as in systemic knockout mice. Photoreceptor-specific Heph knockout indicates that the additional iron in the RPE cells does not result from loss of ferroxidases in the photoreceptors, and Cp and Heph play minor roles in photoreceptors. Instead, loss of ferroxidases in other retinal cells causes retinal iron accumulation and transfer of iron to the RPE cells. Cp and Heph are necessary for iron export from the retina but are not essential for iron import into the retina. Thus, our studies, revise how we think about iron import and export from the retina.

Ferroportin and Exocytoplasmic Ferroxidase Activity Are Required for Brain Microvascular Endothelial Cell Iron Efflux

“…Hp, Fpn, and sCp Are Expressed by hBMVEC-The mechanism of cellular iron efflux from intestinal (21) and lens epithelial cells (22), macrophages (23), and oligodendrocytes (13) involves the functional cooperation of Fpn and an exocytoplasmic ferroxidase, either Hp or Cp. We propose that the same mechanism of iron efflux is true for hBMVEC.…”

Hephaestin and ceruloplasmin facilitate iron metabolism in the mouse kidney

“…Heph KO and Cp KO mouse strains have been previously described83435. The mice were originally obtained from the laboratory of Dr Greg Anderson at the QIMR Berghofer Medical Research Institute (Brisbane, Australia) and were bred and maintained at the Medical School of Nanjing University36.…”

Retinal abnormalities in β-thalassemia major

“…45 ; 82 Iron export from retinal cells is facilitated by multicopper ferroxidases, such as ceruloplasmin (Cp) and its homolog hephaestin (Heph). 96 Their function in iron export has been highlighted in mice with combined deficiency of Cp and Heph leading to age-dependent iron accumulation in the retina and RPE resulting in degeneration. 30 ; 49 The RPE becomes hypertrophic, autofluorescent, and dysplastic.…”