IP3 receptor type 3 and PLCβ2 are co-expressed with taste receptors T1R and T2R in rat taste bud cells

被引:124
作者
Asano-Miyoshi, M
Abe, K
Emori, Y
机构
[1] Univ Tokyo, Fac Sci, Dept Biophys & Biochem, Bunkyo Ku, Tokyo 1130033, Japan
[2] Univ Tokyo, Grad Sch Agr & Life Sci, Dept Appl Biol Chem, Bunkyo Ku, Tokyo 1138657, Japan
[3] Biooriented Technol Res Advancement Inst, Oomiya, Saitama 3310044, Japan
关键词
D O I
10.1093/chemse/26.3.259
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
The Ca2+ signaling cascade has been reported to be activated by many tastants in vertebrate taste systems. Recently we have shown that G(i2) and phospholipase C beta2 (PLC beta2) are co-expressed in a subset of taste bud cells and are possibly involved in Ca2+ triggering of taste signaling in rats. We report here that, as a component downstream of PLC beta2, the type 3 isoform of the inositol 1,4,5-trisphosphate (IP3) receptor (IP(3)R3) is specifically expressed in the same cells as PLC beta2 in rat taste buds. We also show that cells expressing rT2R9, a probable cycloheximide receptor, are included among PLC beta2- and IP(3)R3-positive cells, as in the case of rT1R2, a different type of taste receptor. Our findings indicate that PLC beta2 and IP(3)R3 co-localize together with G(i2) as downstream components of two different types of taste receptors, T1R and T2R, in taste bud cells.
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收藏
页码:259 / 265
页数:7
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