Adenosine transporters in chromaffin cells
Open Access
- 26 May 1986
- journal article
- Published by Wiley in FEBS Letters
- Vol. 201 (1) , 124-128
- https://doi.org/10.1016/0014-5793(86)80583-x
Abstract
Chromaffin cells from bovine adrenal medulla are a useful model to approach adenosine transport and metabolism in neural cells. Dipyridamol has been shown to be an adenosine transport inhibitor with high affinity. To quantify the adenosine transporters a labelled dipyridamol analogue, [14C]dipyridamol acetate, was synthesized. This compound had a K i = 5.3 ± 0.43 nM according to the Dixon method, and 4.58 ± 0.46 nM when the receptor number molarity was taken into account showing, like dipyridamol, a non‐competitive mechanism. The high‐affinity receptors present in chromaffin cells showed a K d = 6.8 ± 0.8 nM and the receptor number was 630000 ± 40000 per cell.Keywords
This publication has 29 references indexed in Scilit:
- Pathways of Protein Secretion in EukaryotesScience, 1985
- Inhibition of exocytosis in bovine adrenal medullary cells by botulinum toxin type DNature, 1985
- Adenosine as a NeuromodulatorAnnual Review of Neuroscience, 1985
- Hypoxanthine transport in mammalian cells: Cell type-specific differences in sensitivity to inhibition by dipyridamole and uridineThe Journal of Membrane Biology, 1984
- Mechanisms of secretion from adrenal chromaffin cellsBiochimica et Biophysica Acta (BBA) - Reviews on Biomembranes, 1984
- Differentiating Adenosine Receptors and Adenosine Uptake Sites in BrainJournal of Receptor Research, 1984
- Insulin-stimulated translocation of glucose transporters in the isolated rat adipose cells: Characterization of subcellular fractionsBiochimica et Biophysica Acta (BBA) - Molecular Cell Research, 1983
- Ecto - adenosine triphosphatase activity at the cholinergic nerve endings of the torpedo electric organLife Sciences, 1983
- Glycogen Metabolism in Bovine Adrenal MedullaJournal of Neurochemistry, 1982
- Adenosine-elicited accumulation of cyclic AMP in brain slices: Potentiation by agents which inhibit uptake of adenosineLife Sciences, 1974