The presence of excitatory amino acid ( E M ) receptors coupled to phosphoinositide metabolism in primary cultures of Muller (glial) cells from the chick retina was established. The order of potency of analogues for stimulating [3Hlinositol phosphate (IP) accumulation was quisqualate (QA) > L-glutam
Excitatory amino acid-induced AP-1 DNA binding activity in müller glia
✍ Scribed by A. M. López-Colomé; J. Murbartián; Dr. Arturo Ortega
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 540 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0360-4012
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✦ Synopsis
The effect of L-glutamate (L-Glu) and its structural analogs N-methyl-D-aspartate (NMDA), quisqualate (QA), and kainate (KA) on the DNA binding activity of the Activator Protein 1 (AP-1) and the Ca*+/cAMP Responsive Element Binding Protein (CREB) families of transcription factors was examined in cultured chick retinal Muller glia cells. L-Glu, NMDA, and KA evoked a dose and time dependent increase in AP-1 DNA binding activity and had no effect on CREB binding. The order of potency for stimulating AP-1 DNA binding was NMDAZGlu>KA>>QA. L-Glu responses were partially blocked by 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX) and by 3-[RS)-2-carboxypiperazin-4-yl)]-propyl-l-phosphonate (CPP) indicating that the increase in DNA binding is mediated both by an a-amino-3-hydroxy-5-methyl-4-isoxazolepropionate (AMPA)/Iow affinity KA and a NMDA subtypes of L-Glu receptors. Since Muller glia L-Glu receptors are probably mediators of the efficacy of the excitatory transmission in the retina, the present findings suggest that a stimulustranscription coupling triggered by L-Glu in the glial cells might have a role in the long-term modulation of these synapses.
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