Shoji N, Kaneta N, Satoh-Kuriwada S, Tsuchiya M, Hashimoto N, Uneyama H, Kawai M, Sasano T
Division of Oral Diagnosis, Tohoku University Graduate School of Dentistry, Sendai, Japan.
Tohoku Fukushi University, Sendai, Japan.
Oral Dis. 2015 Sep;21(6):801-6. doi: 10.1111/odi.12350. Epub 2015 Jun 30.
Expression of taste-related genes in the tongue was analysed to develop a technique for genetic diagnosis of umami taste disorders.
Tissue samples were collected from healthy volunteers by scraping the foliate papillae of the tongue. Immunocytochemistry staining of gustducin, a taste-cell-specific G protein, and gene expression analysis by real-time polymerase chain reaction of β-actin, gustducin (GNAT3) and umami receptors (T1R1, T1R3 and mGluR1) were performed. Changes in umami receptor expression following application of umami substances onto the tongue were analysed.
Gustducin-positive cells were observed in the samples, indicating the presence of taste cells. Gene expression of β-actin, GNAT3, T1R1 and T1R3 was detected in all seven samples tested, while that of mGluR1 was detected in four samples. Sequence analysis by NCBI Blast showed that each polymerase chain reaction product had a 99% rate of identification of its target sequence. Stimulation of the tongue with monosodium glutamate significantly upregulated the gene expression levels of T1R1 and T1R3, indicating that this method can detect alterations in umami-related gene expression.
Evaluation of the expression of the umami receptor genes, T1R1 and T1R3, in the tongue may be clinically useful for objective genetic diagnosis of umami taste disorders.
分析舌中味觉相关基因的表达,以开发一种用于鲜味味觉障碍基因诊断的技术。
通过刮取健康志愿者舌的叶状乳头收集组织样本。进行味觉细胞特异性G蛋白味导素的免疫细胞化学染色,以及通过实时聚合酶链反应对β-肌动蛋白、味导素(GNAT3)和鲜味受体(T1R1、T1R3和mGluR1)进行基因表达分析。分析将鲜味物质应用于舌后鲜味受体表达的变化。
在样本中观察到味导素阳性细胞,表明存在味觉细胞。在所有测试的七个样本中均检测到β-肌动蛋白、GNAT3、T1R1和T1R3的基因表达,而在四个样本中检测到mGluR1的基因表达。通过NCBI Blast进行的序列分析表明每个聚合酶链反应产物对其靶序列的识别率为99%。用谷氨酸钠刺激舌显著上调了T1R1和T1R3的基因表达水平,表明该方法可以检测鲜味相关基因表达的变化。
评估舌中鲜味受体基因T1R1和T1R3的表达可能对鲜味味觉障碍的客观基因诊断具有临床意义。