SHIMADA I, KOGANEZAWA M
Biological Institute, Graduate School of Science, Tohoku University, Aoba-ku, Sendai 980-77, Japan
J Insect Physiol. 1997 Mar;43(3):225-233. doi: 10.1016/s0022-1910(96)00096-0.
A nonhydrolyzable G protein activator (guanosine 5'-O-(3-thiotriphosphate); GTPgammaS) and a G protein inhibitor (guanosine 5'-O-(2-thiodiphosphate); GDPbetaS) 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 GTPgammaS, 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 GDPbetaS 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 GTPgammaS or GDPbetaS, and thus the response to NaCl clearly is not elicited through a G protein-regulated mechanism. Copyright 1997 Elsevier Science Ltd. All rights reserved
通过在0.03%脱氧胆酸盐溶液中用每种试剂处理肉蝇化学感受毛尖端开口下方的感受膜4分钟,将一种不可水解的G蛋白激活剂(鸟苷5'-O-(3-硫代三磷酸); GTPγS)和一种G蛋白抑制剂(鸟苷5'-O-(2-硫代二磷酸); GDPβS)引入肉蝇的唇叶味觉受体细胞。用GTPγS处理后,与仅用脱氧胆酸盐处理后的情况相比,糖受体细胞对D-葡萄糖、D-果糖、L-苯丙氨酸和L-缬氨酸的反应以及盐受体细胞对环磷酸腺苷的反应显著增强。用GDPβS处理会抑制这些反应。这些结果有力地表明这些反应是由G蛋白介导的。然而,盐受体细胞对NaCl的反应不受GTPγS或GDPβS处理的影响,因此对NaCl的反应显然不是通过G蛋白调节机制引发的。版权所有1997爱思唯尔科学有限公司。保留所有权利