MULTIPOTENTIAL STEM-CELLS AND PROGENITORS IN THE VERTEBRATE RETINA

Authors
Citation
Ta. Reh et Em. Levine, MULTIPOTENTIAL STEM-CELLS AND PROGENITORS IN THE VERTEBRATE RETINA, Journal of neurobiology, 36(2), 1998, pp. 206-220
Citations number
104
Categorie Soggetti
Neurosciences
Journal title
ISSN journal
00223034
Volume
36
Issue
2
Year of publication
1998
Pages
206 - 220
Database
ISI
SICI code
0022-3034(1998)36:2<206:MSAPIT>2.0.ZU;2-N
Abstract
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.