TY - JOUR
T1 - The effects of G protein modulators on the labellar taste receptor cells of the fleshfly (boettcherisca peregrina)
AU - Koganezawa, Masayuki
AU - Shimada, Ichiro
N1 - Funding Information:
This study was partly supported by a Grant-in-Aid (Integrated Research Program on the Development of Insect Technology to I.S.) from the Ministry of Agriculture, Forestry and Fisheries, a Grant-in-Aid (to M.K.) from the Ministry of Education, Science and Culture of Japan and JSPS Research Fellowships for Young Scientists (to M.K.).
PY - 1997
Y1 - 1997
N2 - A nonhydrolyzable G protein activator (guanosine 5'-O-(3-thiotriphosphate); GTPγS) and a G protein inhibitor (guanosine 5'-O-(2-thiodiphosphate); GDPβS) were introduced into the labellar taste receptor cells of the fleshfly by treatment of their receptive membranes beneath the tip opening of the chemosensory hair with each reagent in 0.03% deoxycholate solution for 4 min. After treatment with GTPγS, the responses of the sugar receptor cell to D-glucose, D-fructose, L-phenylalanine and L-valine and that of the salt receptor cell to cyclic AMP were markedly enhanced, compared with those after treatment with deoxycholate alone. Treatment with GDPβS depressed these responses. These results strongly suggest that the responses are mediated by G protein. However, the response of the salt receptor cell to NaCl was not affected by treatment with either GTPγS or GDPβS, and thus the response to NaCl clearly is not elicited through a G protein-regulated mechanism.
AB - A nonhydrolyzable G protein activator (guanosine 5'-O-(3-thiotriphosphate); GTPγS) and a G protein inhibitor (guanosine 5'-O-(2-thiodiphosphate); GDPβS) were introduced into the labellar taste receptor cells of the fleshfly by treatment of their receptive membranes beneath the tip opening of the chemosensory hair with each reagent in 0.03% deoxycholate solution for 4 min. After treatment with GTPγS, the responses of the sugar receptor cell to D-glucose, D-fructose, L-phenylalanine and L-valine and that of the salt receptor cell to cyclic AMP were markedly enhanced, compared with those after treatment with deoxycholate alone. Treatment with GDPβS depressed these responses. These results strongly suggest that the responses are mediated by G protein. However, the response of the salt receptor cell to NaCl was not affected by treatment with either GTPγS or GDPβS, and thus the response to NaCl clearly is not elicited through a G protein-regulated mechanism.
KW - Fly
KW - G protein
KW - Taste
KW - Transduction
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U2 - 10.1016/S0022-1910(96)00096-0
DO - 10.1016/S0022-1910(96)00096-0
M3 - Article
AN - SCOPUS:0030786582
SN - 0022-1910
VL - 43
SP - 225
EP - 233
JO - Journal of Insect Physiology
JF - Journal of Insect Physiology
IS - 3
ER -