Skip to main content
The British Journal of Ophthalmology logoLink to The British Journal of Ophthalmology
. 1994 Nov;78(11):863–870. doi: 10.1136/bjo.78.11.863

Improved preservation of human corneal basement membrane following freezing of donor tissue for epikeratophakia.

R D Young 1, W J Armitage 1, P Bowerman 1, S D Cook 1, D L Easty 1
PMCID: PMC504974  PMID: 7848985

Abstract

Current methods for the production of lenticules for epikeratophakia involve rapid freezing, cryolathing, and slow warming of the donor cornea. We have found that this procedure causes structural damage to the epithelial basement membrane in the donor cornea which may subsequently contribute to poor postoperative re-epithelialisation of the implant, leading to graft failure. Endeavouring to overcome these problems, the effects of cryoprotection of donor cornea were investigated, using dimethyl sulphoxide, in conjunction with different cooling and warming rates as part of the protocol for cryolathing. The structural integrity of the epithelial basement membrane zone (BMZ) was then assessed by electron microscopy and by immunofluorescence microscopy using antibodies to types IV and VII collagen, components of the basal lamina and anchoring fibrils respectively, and an antibody to a component of the anchoring filaments. No differences in the pattern of immunostaining for these components were detected, indicating that the composition of the BMZ was unaltered by the different treatment regimens applied. However, electron microscopy showed that preservation of basement membrane ultrastructure was markedly improved when cornea was warmed rapidly rather than slowly, both in cryoprotected and non-cryoprotected tissue. Epithelial cell retention and preservation of stromal architecture appeared superior in cryoprotected samples, while keratocyte structure was heterogeneous throughout the experimental groups. Further work is in progress to assess the efficacy of these protocols in the preservation of keratocyte viability in association with improved basement membrane structure in donor tissue for epikeratophakia.

Full text

PDF
863

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Almeida B. M., Challacombe S. J., Eveson J. W., Smith C. G., Leigh I. M. A novel lamina lucida component of epithelial and endothelial basement membranes detected by LH39 monoclonal antibody. J Pathol. 1992 Mar;166(3):243–253. doi: 10.1002/path.1711660306. [DOI] [PubMed] [Google Scholar]
  2. Azar D. T., Spurr-Michaud S. J., Tisdale A. S., Moore M. B., Gipson I. K. Reassembly of the corneal epithelial adhesion structures following human epikeratoplasty. Arch Ophthalmol. 1991 Sep;109(9):1279–1284. doi: 10.1001/archopht.1991.01080090105032. [DOI] [PubMed] [Google Scholar]
  3. Binder P. S., Baumgartner S. D., Fogle J. A. Histopathology of a case of epikeratophakia (aphakic epikeratoplasty). Arch Ophthalmol. 1985 Sep;103(9):1357–1363. doi: 10.1001/archopht.1985.01050090109044. [DOI] [PubMed] [Google Scholar]
  4. Binder P. S., Beal J. P., Jr, Zavala E. Y. The histopathology of a case of keratophakia. Arch Ophthalmol. 1982 Jan;100(1):101–105. doi: 10.1001/archopht.1982.01030030103009. [DOI] [PubMed] [Google Scholar]
  5. Binder P. S., Zavala E. Y., Deg J., Akers P. H. Refractive keratoplasty. Tissue dyes and cryoprotective solutions. Arch Ophthalmol. 1983 Oct;101(10):1591–1596. doi: 10.1001/archopht.1983.01040020593019. [DOI] [PubMed] [Google Scholar]
  6. Binder P. S., Zavala E. Y. Why do some epikeratoplasties fail? Arch Ophthalmol. 1987 Jan;105(1):63–69. doi: 10.1001/archopht.1987.01060010069033. [DOI] [PubMed] [Google Scholar]
  7. Carter W. G., Ryan M. C., Gahr P. J. Epiligrin, a new cell adhesion ligand for integrin alpha 3 beta 1 in epithelial basement membranes. Cell. 1991 May 17;65(4):599–610. doi: 10.1016/0092-8674(91)90092-d. [DOI] [PubMed] [Google Scholar]
  8. Gipson I. K., Grill S. M., Spurr S. J., Brennan S. J. Hemidesmosome formation in vitro. J Cell Biol. 1983 Sep;97(3):849–857. doi: 10.1083/jcb.97.3.849. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Gipson I. K., Spurr-Michaud S. J., Tisdale A. S. Anchoring fibrils form a complex network in human and rabbit cornea. Invest Ophthalmol Vis Sci. 1987 Feb;28(2):212–220. [PubMed] [Google Scholar]
  10. Gipson I. K., Spurr-Michaud S., Tisdale A., Keough M. Reassembly of the anchoring structures of the corneal epithelium during wound repair in the rabbit. Invest Ophthalmol Vis Sci. 1989 Mar;30(3):425–434. [PubMed] [Google Scholar]
  11. Halliday B. L. Epikeratophakia for aphakia, keratoconus, and myopia. Br J Ophthalmol. 1990 Feb;74(2):67–72. doi: 10.1136/bjo.74.2.67. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Kaufman H. E. The correction of aphakia. XXXVI Edward Jackson Memorial Lecture. Am J Ophthalmol. 1980 Jan;89(1):1–10. doi: 10.1016/0002-9394(80)90222-6. [DOI] [PubMed] [Google Scholar]
  13. Kaufman H. E., Werblin T. P. Epikeratophakia for the treatment of keratoconus. Am J Ophthalmol. 1982 Mar;93(3):342–347. doi: 10.1016/0002-9394(82)90537-2. [DOI] [PubMed] [Google Scholar]
  14. Kratz-Owens K., Huff J. W., Schanzlin D. J. New cryoprotectant for cryorefractive surgery. J Cataract Refract Surg. 1991 Sep;17(5):608–612. doi: 10.1016/s0886-3350(13)81049-8. [DOI] [PubMed] [Google Scholar]
  15. Lee T. J., Wan W. L., Kash R. L., Kratz K. L., Schanzlin D. J. Keratocyte survival following a controlled-rate freeze. Invest Ophthalmol Vis Sci. 1985 Sep;26(9):1210–1215. [PubMed] [Google Scholar]
  16. Lee T. J., Wan W. L., Kash R. L., Kratz K. L., Schanzlin D. J. Keratocyte survival following a controlled-rate freeze. Invest Ophthalmol Vis Sci. 1985 Sep;26(9):1210–1215. [PubMed] [Google Scholar]
  17. Marinkovich M. P., Keene D. R., Rimberg C. S., Burgeson R. E. Cellular origin of the dermal-epidermal basement membrane. Dev Dyn. 1993 Aug;197(4):255–267. doi: 10.1002/aja.1001970404. [DOI] [PubMed] [Google Scholar]
  18. McDonald M. B., Kaufman H. E., Aquavella J. V., Durrie D. S., Hiles D. A., Hunkeler J. D., Keates R. H., Morgan K. S., Sanders D. R. The nationwide study of epikeratophakia for aphakia in adults. Am J Ophthalmol. 1987 Mar 15;103(3 Pt 2):358–365. doi: 10.1016/s0002-9394(14)77758-x. [DOI] [PubMed] [Google Scholar]
  19. McDonald M. B., Kaufman H. E., Aquavella J. V., Durrie D. S., Hiles D. A., Hunkeler J. D., Keates R. H., Morgan K. S., Sanders D. R. The nationwide study of epikeratophakia for myopia. Am J Ophthalmol. 1987 Mar 15;103(3 Pt 2):375–383. doi: 10.1016/s0002-9394(14)77760-8. [DOI] [PubMed] [Google Scholar]
  20. McDonald M. B., Kaufman H. E., Durrie D. S., Keates R. H., Sanders D. R. Epikeratophakia for keratoconus. The nationwide study. Arch Ophthalmol. 1986 Sep;104(9):1294–1300. doi: 10.1001/archopht.1986.01050210048024. [DOI] [PubMed] [Google Scholar]
  21. McDonald M. B., Klyce S. D., Suarez H., Kandarakis A., Friedlander M. H., Kaufman H. E. Epikeratophakia for myopia correction. Ophthalmology. 1985 Oct;92(10):1417–1422. doi: 10.1016/s0161-6420(85)33849-6. [DOI] [PubMed] [Google Scholar]
  22. Olivero D. K., Furcht L. T. Type IV collagen, laminin, and fibronectin promote the adhesion and migration of rabbit lens epithelial cells in vitro. Invest Ophthalmol Vis Sci. 1993 Sep;34(10):2825–2834. [PubMed] [Google Scholar]
  23. Rao G. N., Ganti S., Aquavella J. V. Specular microscopy of corneal epithelium after epikeratophakia. Am J Ophthalmol. 1987 Mar 15;103(3 Pt 2):392–396. doi: 10.1016/s0002-9394(14)77762-1. [DOI] [PubMed] [Google Scholar]
  24. Rich L. F., Friedlander M. H., Kaufman H. E., Granet N. Keratocyte survival in keratophakia lenticules. Arch Ophthalmol. 1981 Apr;99(4):677–680. doi: 10.1001/archopht.1981.03930010677015. [DOI] [PubMed] [Google Scholar]
  25. Rodrigues M., Nirankari V., Rajagopalan S., Jones K., Funderburgh J. Clinical and histopathologic changes in the host cornea after epikeratoplasty for keratoconus. Am J Ophthalmol. 1992 Aug 15;114(2):161–170. doi: 10.1016/s0002-9394(14)73980-7. [DOI] [PubMed] [Google Scholar]
  26. Stock E. L., Kurpakus M. A., Sambol B., Jones J. C. Adhesion complex formation after small keratectomy wounds in the cornea. Invest Ophthalmol Vis Sci. 1992 Feb;33(2):304–313. [PubMed] [Google Scholar]
  27. Yurchenco P. D., Schittny J. C. Molecular architecture of basement membranes. FASEB J. 1990 Apr 1;4(6):1577–1590. doi: 10.1096/fasebj.4.6.2180767. [DOI] [PubMed] [Google Scholar]

Articles from The British Journal of Ophthalmology are provided here courtesy of BMJ Publishing Group

RESOURCES