Studies have suggested that communication between taste cells shapes the gustatory signal before transmission to the brain. To further explore the possibility of intragemmal signal modulation, we adopted an optogenetic approach to stimulate sour-sensitive (Type III) taste cells using mice expressing Cre recombinase under a specific Type III cell promoter, Pkd2l1 (polycystic kidney disease-2-like 1), crossed with mice expressing Cre-dependent channelrhodopsin (ChR2). The application of blue light onto the tongue allowed for the specific stimulation of Type III cells and circumvented the nonspecific effects of chemical stimulation. To understand whether taste modality information is preprocessed in the taste bud before transmission to the sensory nerves, we recorded chorda tympani nerve activity during light and/or chemical tastant application to the tongue. To assess intragemmal modulation, we compared nerve responses to various tastants with or without concurrent light-induced activation of the Type III cells. Our results show that light significantly decreased taste responses to sweet, bitter, salty, and acidic stimuli. On the contrary, the light response was not consistently affected by sweet or bitter stimuli, suggesting that activation of Type II cells does not affect nerve responses to stimuli that activate Type III cells.
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机译:研究表明,味觉细胞之间的交流在传递到大脑之前塑造了味觉信号。为了进一步探索胚内信号调节的可能性,我们采用了一种光遗传学方法,使用在特定 III 型细胞启动子 Pkd2l1 (多囊肾病-2 样 1) 下表达 Cre 重组酶的小鼠与表达 Cre 依赖性通道视紫红质 (ChR2) 的小鼠杂交。将蓝光照射到舌头上可以对 III 型细胞进行特异性刺激,并规避了化学刺激的非特异性作用。为了了解味觉模式信息在传递到感觉神经之前是否在味蕾中进行了预处理,我们记录了在轻度和/或化学味觉应用于舌头期间鼓索神经活动。为了评估 Gemom 内调节,我们比较了神经对各种味觉剂的反应,有或没有同时光诱导的 III 型细胞激活。我们的结果表明,光显着降低了味觉对甜味、苦味、咸味和酸性刺激的反应。相反,光反应并不一致地受到甜味或苦味刺激的影响,这表明 II 型细胞的激活不会影响神经对激活 III 型细胞的刺激的反应。
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