MOLECULAR-BASIS FOR DIFFERENTIAL EXPRESSION OF GLUTAMINE-SYNTHETASE IN RETINA GLIA AND NEURONS

Citation
R. Grossman et al., MOLECULAR-BASIS FOR DIFFERENTIAL EXPRESSION OF GLUTAMINE-SYNTHETASE IN RETINA GLIA AND NEURONS, Molecular brain research, 21(3-4), 1994, pp. 312-320
Citations number
49
Categorie Soggetti
Neurosciences
Journal title
ISSN journal
0169328X
Volume
21
Issue
3-4
Year of publication
1994
Pages
312 - 320
Database
ISI
SICI code
0169-328X(1994)21:3-4<312:MFDEOG>2.0.ZU;2-W
Abstract
Glutamine synthetase (GS) is a differentiation marker of retina glial cells. It is expressed in the chicken neural retina at a particularly high level, is inducible by glucocorticoids and is always confined to Muller glia. This study investigated the molecular basis for tissue an d cell-type specific expression of the GS gene. A high level of os exp ression in the retina was found to coincide with the accumulation of a relatively high lever of GS mRNA in this tissue. The gliatoxic agent alpha-aminoadipic acid, which can selectively destroy glia cells, was used to demonstrate that restriction of os induction to Muller glia is controlled at a transcriptional level. Cortisol could induce accumula tion of GS mRNA and transcription of the GS gene in Muller glia but no t in retina neurons. Glia and neurons were also found to differ in the ir ability to express the glucocorticoid inducible CAT construct, p De lta G46TCO, which is controlled by a 'simple GRE' promoter. When intro duced into cells of retina tissue, this construct was cortisol-inducib le in glia whereas in neurons it was only slightly inducible or not at all. Introduction of a glucocorticoid receptor expression vector into the cells facilitated induction of the CAT construct in neurons. Anal ysis by immunoblotting revealed that expression of the glucocorticoid receptor protein is predominantly restricted to Muller glia. These res ults suggest that differential levels of glucocorticoid receptor expre ssion in glia and neurons might be the basis for cell-type specific in duction of GS.