| Literature DB >> 9263598 |
J P Kapfhammer1, F Christ, M E Schwab.
Abstract
In the adult retina, the growth-associated protein GAP-43 is exclusively present in three distinct sublaminae of the inner plexiform layer. During postnatal development, it is transiently expressed in the optic nerve fibers. No conclusions about the GAP-43 expressing cells can be derived from immunohistochemical stainings because GAP-43 protein is rapidly transported into the distal neuronal processes. We have combined immunohistochemistry to study the protein expression of GAP-43 and non-radioactive in situ hybridization to study the cellular expression of GAP-43 in the rat retina. We have found that in the mature retina GAP-43 mRNA is present only in retinal ganglion cells and in a small subset of cells of the inner nuclear layer. During postnatal development, no cells besides retinal ganglion cells and a subpopulation of cells in the inner nuclear layer express GAP-43 mRNA. Double staining experiments with tyrosine hydroxylase (TH) immunohistochemistry and GAP-43 in situ hybridization showed that GAP-43 expressing cells in the inner nuclear layer are immunoreactive for TH. They are most probably dopaminergic amacrine cells. Our results show that GAP-43 expression in the retina is restricted to very few cell types. They suggest that TH-positive cells (probably dopaminergic amacrine cells) retain a higher degree of structural plasticity in the adult retina.Entities:
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Year: 1997 PMID: 9263598 DOI: 10.1016/s0165-3806(97)00081-3
Source DB: PubMed Journal: Brain Res Dev Brain Res ISSN: 0165-3806