Narukawa Masataka, Minamisawa Eiko, Hayashi Yukako
Graduate School of Agriculture, Kyoto University, Kyoto, Japan.
Neuroreport. 2009 Jul 1;20(10):936-40. doi: 10.1097/wnr.0b013e32832c5e80.
To clarify the components involved in mouse intracellular bitter transduction in the mouse, we investigated the expression patterns of transduction components and the contribution of intracellular Ca2+ stores. Of 64 cells responding to bitter compounds, 63% of the cells expressed the taste tissue-specific G-protein alpha-gustducin. Of the alpha-gustducin immunoreactive cells, 78% expressed IP3R3, a receptor that mediates Ca2+ release from the intracellular store. When intracellular Ca2+ was depleted by treatment with the inhibitor thapsigargin, 83% of the taste cells lost their response to bitter. These data suggest that bitterness transduction involves the release of Ca2+ from intracellular stores.
为了阐明小鼠细胞内苦味转导所涉及的成分,我们研究了转导成分的表达模式以及细胞内钙库的作用。在对苦味化合物有反应的64个细胞中,63%的细胞表达了味觉组织特异性G蛋白α-味导素。在α-味导素免疫反应性细胞中,78%表达了IP3R3,一种介导细胞内钙库释放钙离子的受体。当用抑制剂毒胡萝卜素处理使细胞内钙离子耗尽时,83%的味觉细胞失去了对苦味的反应。这些数据表明,苦味转导涉及细胞内钙库释放钙离子。