Regulation Of Cyclic Amp By Extracellular Atp In Cultured Brain Capillary Endothelial Cells

1 In primary unpassaged rat brain capillary endothelial cell cultures (RBECs), using reverse-transcriptase PCR with primers specific for P2Y receptor subtypes, we detected mRNA for P2Y(2), P2Y(4) and P2Y(6), but not P2Y(1) receptors.2 None of the various nucleotides tested reduced forskolin elevated cyclic AMP levels in RBECs. ATP and ATP gamma S, as well as adenosine, enhanced cyclic AMP accumulation in the presence of forskolin.3 Comparison of the concentration response curves to ATP gamma S with those for ATP and adenosine, at different incubation times, indicated that the response to purine nucleotides was not wholly dependent on conversion to adenosine. Adenosine deaminase abolished the response to adenosine but only reduced the response to ATP by about 50%. These results suggest the participation of a receptor responsive to nucleotides.4 Isobutylmethylxanthine and 8-sulphophenyltheophylline prevented the cyclic AMP response, while neither 8-cyclopentyl-1,3-dipropylxanthine nor SCH58261 were effective antagonists. 2-chloradenosine gave a robust response, but neither 2-chloro-N-6-cyclopentyladenosine nor CGS 21680 were agonists.5 These results show that adenosine and ATP can elevate the cyclic AMP levels of brain endothelial cells by acting on receptors which have a pharmacology apparently distinct from known P2Y and adenosine receptors.