The vertebrate retina is derived from paired evaginations from the neu
ral tube in embryonic development and is initially produced by progeni
tor cells similar to those that generate the neurons and glia of other
areas of the central nervous system. In some amphibians and fish, the
retina continues to grow along with the eye throughout the life of th
e animal. The new retinal cells are added at the ciliary margin of the
eye from the mitotic activity of neural/ glial stem cells in a region
known as the germinal zone and are seamlessly incorporated into the e
xisting retinal circuitry. Little is known about the cell or molecular
biology of these stem cells; however, studies of retinal progenitor c
ells in chick and mammalian embryos have led to the identification of
several factors that control their proliferation. Moreover, studies of
retinal regeneration have shown that retinal stem cells can also be d
erived from two or perhaps three additional sources after retinal dama
ge: (a) the retinal pigmented epithelium (RPE) in amphibians and embry
onic chicks and mammals; (b) a specialized rod progenitor in fish; and
(c) the Muller glial cells. While there is currently no evidence for
a neural/glial stem cell in the adult mammalian retina, and the retina
of the mature mammal does not show regenerative capacity after damage
, there is a possibility for the reinitiation of stem cell potential a
t the peripheral retinal margin, from the RPE or from the Muller glial
cells. The application of information derived from the studies of ret
inal progenitor cells in developing organisms should soon provide a te
st of these possibilities, (C) 1998 John Wiley & Sons, Inc.