par Torfs, Herbert;Shariatmadari, R;Guerrero, Flor María;Parmentier, Marc
;Poels, Jeroen;Van Poyer, W;Swinnen, E;De Loof, Arnold;Akerman, Karl E;Vanden Broeck, Jozef
Référence Journal of neurochemistry, 74, 5, page (2182-2189)
Publication Publié, 2000-05

Référence Journal of neurochemistry, 74, 5, page (2182-2189)
Publication Publié, 2000-05
Article révisé par les pairs
Résumé : | STKR is an insect G protein-coupled receptor, cloned from the stable fly Stomoxys calcitrans. It displays sequence similarity to vertebrate tachykinin [or neurokinin (NK)] receptors. Functional expression of the cloned STKR cDNA was obtained in cultured Drosophila melanogaster Schneider 2 (S2) cells. Insect tachykinin-like peptides or "insectatachykinins," such as Locusta tachykinin (Lom-TK) III, produced dose-dependent calcium responses in stably transfected S2-STKR cells. Vertebrate tachykinins (or neurokinins) did not evoke any effect at concentrations up to 10(-5) M, but an antagonist of mammalian neurokinin receptors, spantide II, inhibited the Lom-TK III-induced calcium response. Further analysis showed that the agonist-induced intracellular release of calcium ions was not affected by pretreatment of the cells with pertussis toxin. The calcium rise was blocked by the phospholipase C inhibitor U73122. In addition, Lom-TK III was shown to have a stimulatory effect on the accumulation of both inositol 1,4,5-trisphosphate and cyclic AMP. These are the same second messengers that are induced in mammalian neurokinin-dependent signaling processes. |