Purpose Confocal microscopy can give images of high magnification and
resolution in undisturbed living tissue. It provides new information a
bout the cellular structure of the cornea. Our aim was to measure the
density, size and distribution of keratocytes. Methods Healthy cornea
in four subjects was examined using tandem scanning confocal microscop
y. Methods for digital analysis of images were developed. Results Kera
tocyte density in confocal cross-sections was greatest immediately und
er Bowman's membrane (maximum 800 cells/mm(2)) and decreased sharply t
owards posterior cornea (minimum 65 cells/mm(2)). Cross-sectional cell
size ranged from 78 to 211 mu m(2), but did not correlate with depth
in the tissue. Conclusions Results are consistent with those of earlie
r work using histological and biochemical techniques in isolated tissu
e. The methods we have developed enable studies of ongoing processes i
n conscious humans and can be used to examine diseased tissue as well
as the response to injury.