Developmental regulation of the nuclear ferritoid-ferritin complex of avian corneal epithelial cells: Roles of systemic factors and thyroxine

Experimental Eye Research

Volumn 89, Issue 6, 2009, Pages 854-862

  Beazley, Kelly E ^a   Canner, James P ^a   Linsenmayer, Thomas F ^a  

^a TUFTS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

CAM; corneal epithelium; ferritin; ferritoid; thyroxine

Indexed keywords

FERRITIN; FERRITOID; METALLOPROTEIN; THYROXINE; UNCLASSIFIED DRUG;

ANIMAL TISSUE; ARTICLE; CHORIOALLANTOIS; COMPLEX FORMATION; CONTROLLED STUDY; CORNEA EPITHELIUM; EMBRYO; EPITHELIUM CELL; FOWL; HORMONE ACTION; NONHUMAN; OXIDATIVE STRESS; PRIORITY JOURNAL; PROTEIN SYNTHESIS; REGULATORY MECHANISM; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION;

ANIMALS; CELL NUCLEUS; CHICK EMBRYO; CORNEAL TRANSPLANTATION; CULTURE MEDIA, SERUM-FREE; DNA-BINDING PROTEINS; EMBRYONIC DEVELOPMENT; EPITHELIUM, CORNEAL; EYE PROTEINS; FERRITINS; NUCLEOCYTOPLASMIC TRANSPORT PROTEINS; ORGAN CULTURE TECHNIQUES; SERUM; THYROXINE; TRIIODOTHYRONINE;

EID: 70350714453     PISSN: 00144835     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.exer.2009.07.007     Document Type: Article

References (29)

1. Beazley K.E., Nurminskaya M., Talbot C.J., and Linsenmayer T.F. Corneal epithelial nuclear ferritin: developmental regulation of ferritin and its nuclear transporter ferritoid. Dev. Dyn. 237 (2008) 2529-2541
2. Cai C.X., Birk D.E., and Linsenmayer T.F. Ferritin is a developmentally-regulated nuclear protein of avian corneal epithelial cells. J. Biol. Chem. 272 (1997) 12831-12839
3. Cai C.X., Birk D.E., and Linsenmayer T.F. Nuclear ferritin protects DNA from UV damage in corneal epithelial cells. Mol. Biol. Cell 9 (1998) 1037-1051
4. Cai C.X., Ching A., Lagace C., and Linsenmayer T. Nuclear ferritin-mediated protection of corneal epithelial cells from oxidative damage to DNA. Dev. Dyn. 237 (2008) 2676-2683
5. Conrad A.H., Zhang Y.T., Walker A.R., Olberding L.A., Hanzlick A., Zimmer A.J., Morffi R., and Conrad G.W. Thyroxine affects expression of KSPG-related genes, the carbonic anhydrase II gene, and KS sulfation in the embryonic chicken cornea. Invest. Ophthalmol. Vis. Sci. 47 (2006) 120-132
6. Cotsarelis G., Cheng S.-Z., Dong G., Sun T.-T., and Lavker R.M. Existence of slow-cycling limbal epithelial basal cells that can be preferentially stimulated to proliferate: implications on epithelial stem cells. Cell 57 (1989) 201-209
7. Deshpande U.R., and Nadkarni G.D. Relation between thyroid status and ferritin metabolism in rats. Thyroidology 4 (1992) 93-97
8. Grant R.A., Filman D.J., Finkel S.E., Kolter R., and Hogle J.M. The crystal structure of Dps, a ferritin homolog that binds and protects DNA. Nat. Struct. Biol. 5 (1998) 294-303
9. Hamburger V., and Hamilton H.L. A series of normal stages in the development of the chick embryo. J. Morphol. 88 (1951) 49-92
10. Hart R.W., Setlow R.B., and Woodhead A.D. Evidence that pyrimidine dimers in DNA can give rise to tumors. Proc. Natl. Acad. Sci. U.S.A. 74 (1977) 5574-5578
11. Henle E.S., Luo Y., Gassmann W., and Linn S. Oxidative damage to DNA constituents by iron-mediated fenton reactions. The deoxyguanosine family. J. Biol. Chem. 271 (1996) 21177-21186
12. Kinoshita S., Adachi W., Sotozono C., Nishida K., Yokoi N., Quantock A.J., and Okubo K. Characteristics of the human ocular surface epithelium. Prog. Retin. Eye Res. 20 (2001) 639-673
13. Leedman P.J., Stein A.R., Chin W.W., and Rogers J.T. Thyroid hormone modulates the interaction between iron regulatory proteins and the ferritin mRNA iron-responsive element. J. Biol. Chem. 271 (1996) 12017-12023
14. Linsenmayer T.F., Cai C.X., Millholland J.M., Beazley K.E., and Fitch J.M. Nuclear ferritin in corneal epithelial cells: tissue-specific nuclear transport and protection from UV-damage. Prog. Retin. Eye Res. 24 (2005) 139-159
15. Longini M., Perrone S., Vezzosi P., Marzocchi B., Kenanidis A., Centini G., Rosignoli L., and Buonocore G. Association between oxidative stress in pregnancy and preterm premature rupture of membranes. Clin. Biochem. 40 (2007) 793-797
16. Luo Y., Henle E.S., and Linn S. Oxidative damage to DNA constituents by iron-mediated fenton reactions. The deoxycytidine family. J. Biol. Chem. 271 (1996) 21167-21176
17. Majo F., Rochat A., Nicolas M., Jaoude G.A., and Barrandon Y. Oligopotent stem cells are distributed throughout the mammalian ocular surface. Nature 456 (2008) 250-254
18. Millholland J.M., Fitch J.M., Cai C.X., Gibney E.P., Beazley K.E., and Linsenmayer T.F. Ferritoid, a tissue-specific nuclear transport protein for ferritin in corneal epithelial cells. J. Biol. Chem. 278 (2003) 23963-23970
19. Nurminskaya M., Talbot C.J., Nurminsky D.I., Beazley K.E., and Linsenmayer T.F. Nuclear ferritin: a ferritoid-ferritin complex in corneal epithelial cells. Invest. Ophthalmol. Vis. Sci. (2009)
20. Pantopoulos K. Iron metabolism and the IRE/IRP regulatory system: an update. Ann. N.Y. Acad. Sci. 1012 1-13 (2004) 1-13
21. Prati M., Calvo R., Morreale G., and Morreale de Escobar G. L-thyroxine and 3,5,3′-triiodothyronine concentrations in the chicken egg and in the embryo before and after the onset of thyroid function. Endocrinology 130 (1992) 2651-2659
22. Samuels H.H., Tsai J.S., and Cintron R. Thyroid hormone action: a cell-culture system responsive to physiological concentrations of thyroid hormones. Science 181 (1973) 1253-1256
23. Shimmura S., Suematsu M., Shimoyama M., Tsubota K., Oguchi Y., and Ishimura Y. Subthreshold UV radiation-induced peroxide formation in cultured corneal epithelial cells: the protective effects of lactoferrin. Exp. Eye Res. 63 (1996) 519-526
24. Smolin G., and Thoft R.A. The Cornea: Scientific Foundations and Clinical Practice (1987), Little, Brown and Company, Boston/Toronto
25. Stohs S.J., and Bagchi D. Oxidative mechanisms in the toxicity of metal ions. Free Radic. Biol. Med. 18 (1995) 321-336
26. Thommes R.C., Fitzsimons E.J., Davis M., and Woods J.E. Immunocytochemical demonstration of T4 content and TSH-binding by cells of the thyroid of the developing chick embryo. Gen. Comp. Endocrinol. 85 (1992) 79-85
27. Zak N.B., and Linsenmayer T.F. Monoclonal antibodies against developmentally regulated corneal antigens. Dev. Biol. 99 (1983) 373-381
28. Zak N.B., and Linsenmayer T.F. Analysis of corneal development with monoclonal antibodies. I Differentiation in isolated corneas. Dev. Biol. 108 (1985) 443-454
29. Zak N.B., and Linsenmayer T.F. Analysis of corneal development with monoclonal antibodies. II Tissue autonomy in cornea-skin recombinants. Dev. Biol. 108 (1985) 455-464