Although retinal neurons usually last the entire lifetime of an indivi
dual, many innate genetic and developmental errors and external stimul
i can reduce their longevity leading to loss of visual acuity or blind
ness. Similarly, the lens, largely composed of denucleated fiber cells
must remain transparent for life if vision is to remain clear. Apopto
sis of retinal neurons and newly generated lens fiber cells contribute
s to retinal degeneration and cataract formation, respectively, in bot
h humans and experimental mammals. The apoptosis is triggered by many
stimuli in addition to inherited mutations and may be amenable to phar
macologic amelioration. These studies not only provide new clinical in
sights but also the opportunity to investigate the molecular pathways
leading to apoptosis in an organ that is not required for survival. Th
e eye, becomes, therefore, an important organ for evaluation of theori
es of apoptosis in vivo.