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氨氯地平敏感的氯化钠味觉反应与小鼠上皮钠通道α亚基的基因变异有关。

Amiloride-sensitive NaCl taste responses are associated with genetic variation of ENaC alpha-subunit in mice.

作者信息

Shigemura Noriatsu, Ohkuri Tadahiro, Sadamitsu Chiharu, Yasumatsu Keiko, Yoshida Ryusuke, Beauchamp Gary K, Bachmanov Alexander A, Ninomiya Yuzo

机构信息

Section of Oral Neuroscience, Graduate School of Dental Science, Kyushu University, Fukuoka, Japan.

出版信息

Am J Physiol Regul Integr Comp Physiol. 2008 Jan;294(1):R66-75. doi: 10.1152/ajpregu.00420.2007. Epub 2007 Oct 31.

Abstract

An epithelial Na(+) channel (ENaC) is expressed in taste cells and may be involved in the salt taste transduction. ENaC activity is blocked by amiloride, which in several mammalian species also inhibits taste responses to NaCl. In mice, lingual application of amiloride inhibits NaCl responses in the chorda tympani (CT) gustatory nerve much stronger in the C57BL/6 (B6) strain than in the 129P3/J (129) strain. We examined whether this strain difference is related to gene sequence variation or mRNA expression of three ENaC subunits (alpha, beta, gamma). Real-time RT-PCR and in situ hybridization detected no significant strain differences in expression of all three ENaC subunits in fungiform papillae. Sequences of the beta- and gammaENaC subunit genes were also similar in the B6 and 129 strains, but alphaENaC gene had three single nucleotide polymorphisms (SNPs). One of these SNPs resulted in a substitution of arginine in the B6 strain to tryptophan in the 129 strain (R616W) in the alphaENaC protein. To examine association of this SNP with amiloride sensitivity of CT responses to NaCl, we produced F(2) hybrids between B6 and 129 strains. Amiloride inhibited CT responses to NaCl in F(2) hybrids with B6/129 and B6/B6 alphaENaC R616W genotypes stronger than in F(2) hybrids with 129/129 genotype. This suggests that the R616W variation in the alphaENaC subunit affects amiloride sensitivity of the ENaC channel and provides evidence that ENaC is involved in amiloride-sensitive salt taste responses in mice.

摘要

上皮钠通道(ENaC)在味觉细胞中表达,可能参与咸味转导。ENaC活性被氨氯吡咪阻断,在几种哺乳动物中,氨氯吡咪也抑制对NaCl的味觉反应。在小鼠中,舌部应用氨氯吡咪对鼓索神经(CT)味觉神经中NaCl反应的抑制作用,在C57BL/6(B6)品系中比在129P3/J(129)品系中更强。我们研究了这种品系差异是否与三个ENaC亚基(α、β、γ)的基因序列变异或mRNA表达有关。实时逆转录聚合酶链反应(RT-PCR)和原位杂交检测到菌状乳头中所有三个ENaC亚基的表达在品系间无显著差异。β-和γ-ENaC亚基基因的序列在B6和129品系中也相似,但α-ENaC基因有三个单核苷酸多态性(SNP)。其中一个SNP导致α-ENaC蛋白中B6品系的精氨酸替换为129品系的色氨酸(R616W)。为了研究这个SNP与CT对NaCl反应的氨氯吡咪敏感性的关联,我们培育了B6和129品系之间的F2杂种。氨氯吡咪对具有B6/129和B6/B6 α-ENaC R616W基因型的F2杂种中CT对NaCl反应的抑制作用,比具有129/129基因型的F2杂种更强。这表明α-ENaC亚基中的R616W变异影响ENaC通道的氨氯吡咪敏感性,并提供了ENaC参与小鼠氨氯吡咪敏感的咸味反应的证据。

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