The cornea is the clear window through which the eye sees. The studies in this grant proposal are designed to answer questions concerning the cells of the cornea, how they respond to preservation, transplantation, disease, and topical drug therapy, as well as how they protect themselves from ambient ultraviolet light. Most of the studies are concerned with human corneas. Human corneal cells will be photographed and analyzed in vivo in transplanted corneas, in corneas with keratoconus and Fuchs' dystrophy, and in corneas after long-term contact lens wear or topical ocular hypertensive therapy. A tandem scanning confocal microscope will be used to image the stromal keratocytes in these conditions and determine their number. The instrument will also determine epithelial thickness and stromal light reflectivity. A endothelial specular microscope will be used to image and count the endothelial cells. A unique series of 500 consecutive patients with corneal transplants will be examined at 5-year intervals 15, 20, and 25 years after transplantation in order to learn the long-term course of these operations and the importance of various preoperative and surgical factors. Apoptosis (programmed cell death) in newly transplanted human corneas and human corneal cryopreservation will be studied in a xenograft model. Finally, the high concentrations of ascorbate (vitamin C) in the corneal epithelium will be investigated in humans, guinea pigs, and rabbits as a possible mechanism by which the ocular cells are protected from the damaging effects of ultraviolet light.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY002037-23
Application #
6384284
Study Section
Visual Sciences A Study Section (VISA)
Program Officer
Fisher, Richard S
Project Start
1978-08-01
Project End
2003-08-31
Budget Start
2001-09-01
Budget End
2002-08-31
Support Year
23
Fiscal Year
2001
Total Cost
$315,560
Indirect Cost
Name
Mayo Clinic, Rochester
Department
Type
DUNS #
City
Rochester
State
MN
Country
United States
Zip Code
55905
McLaren, Jay W; Bourne, William M; Maguire, Leo J et al. (2015) Changes in Keratocyte Density and Visual Function Five Years After Laser In Situ Keratomileusis: Femtosecond Laser Versus Mechanical Microkeratome. Am J Ophthalmol 160:163-70
Klingler, Kyle N; McLaren, Jay W; Bourne, William M et al. (2012) Corneal endothelial cell changes 5 years after laser in situ keratomileusis: femtosecond laser versus mechanical microkeratome. J Cataract Refract Surg 38:2125-30
Ahuja, Yachna; Baratz, Keith H; McLaren, Jay W et al. (2012) Decreased corneal sensitivity and abnormal corneal nerves in Fuchs endothelial dystrophy. Cornea 31:1257-63
Calvo, Ramón; McLaren, Jay W; Hodge, David O et al. (2010) Corneal aberrations and visual acuity after laser in situ keratomileusis: femtosecond laser versus mechanical microkeratome. Am J Ophthalmol 149:785-93
McLaren, Jay W; Bourne, William M; Patel, Sanjay V (2010) Automated assessment of keratocyte density in stromal images from the ConfoScan 4 confocal microscope. Invest Ophthalmol Vis Sci 51:1918-26
Patel, Sanjay V; Diehl, Nancy N; Hodge, David O et al. (2010) Donor risk factors for graft failure in a 20-year study of penetrating keratoplasty. Arch Ophthalmol 128:418-25
Patel, Sanjay V; McLaren, Jay W; Kittleson, Katrina M et al. (2010) Subbasal nerve density and corneal sensitivity after laser in situ keratomileusis: femtosecond laser vs mechanical microkeratome. Arch Ophthalmol 128:1413-9
McLaren, Jay W; Bourne, William M; Patel, Sanjay V (2010) Standardization of corneal haze measurement in confocal microscopy. Invest Ophthalmol Vis Sci 51:5610-6
Patel, Sangita P; Bourne, William M (2009) Corneal endothelial cell proliferation: a function of cell density. Invest Ophthalmol Vis Sci 50:2742-6
Patel, Sanjay V; Bourne, William M (2009) Corneal endothelial cell loss 9 years after excimer laser keratorefractive surgery. Arch Ophthalmol 127:1423-7

Showing the most recent 10 out of 129 publications