Apoptosis is a selective event of physiological cell deletion that pla
ys a crucial role in the development of numerous tissues, including th
e retina. In this paper we report the occurrence of apoptosis in epire
tinal membranes derived from patients with proliferative vitreoretinop
athy (PVR). Detection of apoptosis was performed by an in situ DNA-end
-labeling technique using terminal transferase-mediated deoxyuridine t
riphosphate (dUTP) incorporation. Apoptotic nuclei exhibiting chromati
n condensation and fragmentation were also identified by acridine oran
ge fluorescence. Apoptosis was detected in varying numbers of cells. T
he typical appearance of apoptotic nuclei, including nuclear chromatin
condensation, was detected scattered inhomogeneously throughout the e
piretinal membranes, in clusters, or even in single cells. Induction o
f apoptosis in human retinal pigment epithelial (RPE) cells by daunomy
cin could be demonstrated by in situ DNA end labeling and by quantitat
ive determination of cytoplasmatic histone-associated DNA fragments us
ing a photometric enzyme immunoassay. Since apoptosis has been shown t
o be an important factor in the growth control of various untransforme
d and neoplastic cell populations, the pharmacological induction of ap
optosis in epiretinal membranes could result in a new approach toward
inhibiting cellular proliferation in PVR.