Special Issue Research Article
Nuclear ferritin-mediated protection of corneal epithelial cells from oxidative damage to DNA
Article first published online: 25 MAR 2008
Copyright © 2008 Wiley-Liss, Inc.
Special Issue: Special Focus on the Extracellular Matrix, in Memory of Dr. Elizabeth D. Hay
Volume 237, Issue 10, pages 2676–2683, October 2008
How to Cite
Cai, C., Ching, A., Lagace, C. and Linsenmayer, T. (2008), Nuclear ferritin-mediated protection of corneal epithelial cells from oxidative damage to DNA. Dev. Dyn., 237: 2676–2683. doi: 10.1002/dvdy.21494
- Issue published online: 24 SEP 2008
- Article first published online: 25 MAR 2008
- Manuscript Accepted: 25 JAN 2008
- NIH. Grant Number: EY13127
- corneal epithelial cells;
- oxidative damage;
- reactive oxygen species
We previously obtained evidence that ferritin is a nuclear protein in embryonic avian corneal epithelial (CE) cells, and that the ferritin in this site protects DNA from UV-induced damage. UV irradiation is known to produce reactive oxygen species (ROS) and ferritin is known to ameliorate further oxidative damage by sequestering free iron, thus decreasing the formation of hydroxyl radicals through the Fenton reaction. Here we present evidence that nuclear ferritin can similarly prevent damage by the ROS, H2O2. These results, when coupled with our previous ones showing that nuclear ferritin appears in the CE early in its development, raises the possibility that this ferritin may serve two protective roles. The initial one would be during embryonic development to protect the CE from ROS endogenously produced by the embryo itself (e.g., H2O2; the latter one would be post-hatching to protect the CE from environmentally produced oxidative insults (e.g., from U.V. light). Developmental Dynamics 237:2676–2683, 2008. © 2008 Wiley-Liss, Inc.