When thin optically transparent specimens are grown on reflective subs
trates, contrast in reflection confocal microscopy is markedly enhance
d. This enhanced contrast allows for the visualization of the thin fil
opodia and organelles contained within the neuritic processes of PC12
cells in culture. The characteristics of this contrast enhancement sug
gest that it arises because of interference between light scattered fr
om rile specimen and coherently backscattered illumination reflected o
ff the substrate. This technique provides a method for visualizing liv
ing cells or other similarly transparent objects on opaque substrates
in a nondestructive manner.