日本生理学会大会発表要旨集
セッションID: 1P234
会議情報
S125 Ionic channels & receptors
G蛋白質共役受容体THTRのリガンド探索
高尾 恭一高尾 哲也風間 宏美吉田 友佳酒井 麻美子武田 Shigeki芳賀 達也國分 眞一朗Suga 比奈子
著者情報
会議録・要旨集 フリー

詳細
抄録
Background: Computer searches for human genome revealed a family of novel G-protein coupled receptors, THTRs, which are highly homologous to a family of bitter taste receptors, T2Rs (Takeda et al. (2002) FEBS Lett. 520, 97). We have previously cloned all human THTR and T2R genes. We have also shown that the assay system using receptor-Gα16 fusion proteins is an effective method for ligand screening. In this study, this assay system was utilized to identify ligands of THTRs and T2Rs. Method: THTR- and T2R-Gα16 fusion protein cDNA were constructed and stably expressed in CHO cells. The cells were stimulated with various stimulants, including tastants. Subsequently, The supernatant of the cells was collected and prostaglandin E2 generation was measured using an enzyme immunoassay kit. Tissue distribution of receptors was investigated by RT-PCR. Results & Conclusion: THTR 5 was highly expressed in tongue epithelia. In cells, expressing THTR5-Gα16 fusion protein, glucose induced marked prostaglandin E2 generation. These data suggested that THTR5 might function as glucose receptor in tongue epithelia. [Jpn J Physiol 54 Suppl:S129 (2004)]
著者関連情報
© 2004 日本生理学会
前の記事 次の記事
feedback
Top