Conflict of interest: JTH has recently given a scientific talk to Genentech and received an honorarium. The other authors report no financial interest related to this manuscript.
Decreased membrane complement regulators in the retinal pigmented epithelium contributes to age-related macular degeneration
Article first published online: 24 JAN 2013
Copyright © 2012 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
The Journal of Pathology
Volume 229, Issue 5, pages 729–742, April 2013
How to Cite
Ebrahimi, K. B., Fijalkowski, N., Cano, M. and Handa, J. T. (2013), Decreased membrane complement regulators in the retinal pigmented epithelium contributes to age-related macular degeneration. J. Pathol., 229: 729–742. doi: 10.1002/path.4128
- Issue published online: 13 MAR 2013
- Article first published online: 24 JAN 2013
- Accepted manuscript online: 24 OCT 2012 02:47AM EST
- Manuscript Accepted: 7 OCT 2012
- Manuscript Revised: 2 OCT 2012
- Manuscript Received: 9 MAY 2012
- age-related macular degeneration;
- oxidative stress
Dysregulated complement is thought to play a central role in age-related macular degeneration (AMD) pathogenesis, but the specific mechanisms have yet to be determined. In maculae of AMD specimens, we found that the complement regulatory protein, CD59, was increased in regions of uninvolved retinal pigmented epithelium (RPE) of early AMD, but decreased in the RPE overlying drusen and in geographic atrophy, an advanced form of AMD. While CD46 immunostaining was basolaterally distributed in the RPE of unaffected controls, it was decreased in diseased areas of early AMD samples. Since oxidized low-density lipoproteins (oxLDL) collect in drusen of AMD and are a known complement trigger, we treated ARPE-19 cells with oxLDL and found that cellular CD46 and CD59 proteins were decreased by 2.9- and nine-fold (p < 0.01), respectively. OxLDLs increased complement factor B mRNA and Bb protein, but not factor D, I or H. OxLDLs increased C3b, but not C3a, C5 or C5b-9. C5b-9 was increased by 27% (p < 0.01) when the medium was supplemented with human serum, which was sufficient to induce poly(ADP-ribose) polymerase cleavage, a marker of apoptosis. The decreased levels of CD46 and CD59 were in part explained by their release in exosomal and apoptotic membranous particles. In addition, CD59 was partially degraded through activation of IRE1α. Collectively, these results suggest that a combination of impaired complement regulators results in inadequately controlled complement by the RPE in AMD that induces RPE damage. Copyright © 2012 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.