Sun Chengsan, Hummler Edith, Hill David L
Department of Psychology, University of Virginia, Charlottesville, Virginia 22904-4400, and.
Pharmacology and Toxicology Department, Faculty of Biology and Medicine, University of Lausanne, CH-1005 Lausanne, Switzerland.
J Neurosci. 2017 Jan 18;37(3):660-672. doi: 10.1523/JNEUROSCI.2913-16.2016.
Neuronal activity plays a key role in the development of sensory circuits in the mammalian brain. In the gustatory system, experimental manipulations now exist, through genetic manipulations of specific taste transduction processes, to examine how specific taste qualities (i.e., basic tastes) impact the functional and structural development of gustatory circuits. Here, we used a mouse knock-out model in which the transduction component used to discriminate sodium salts from other taste stimuli was deleted in taste bud cells throughout development. We used this model to test the hypothesis that the lack of activity elicited by sodium salt taste impacts the terminal field organization of nerves that carry taste information from taste buds to the nucleus of the solitary tract (NST) in the medulla. The glossopharyngeal, chorda tympani, and greater superficial petrosal nerves were labeled to examine their terminal fields in adult control mice and in adult mice in which the α-subunit of the epithelial sodium channel was conditionally deleted in taste buds (αENaC knockout). The terminal fields of all three nerves in the NST were up to 2.7 times greater in αENaC knock-out mice compared with the respective field volumes in control mice. The shapes of the fields were similar between the two groups; however, the density and spread of labels were greater in αENaC knock-out mice. Overall, our results show that disruption of the afferent taste signal to sodium salts disrupts the normal age-dependent "pruning" of all terminal fields, which could lead to alterations in sensory coding and taste-related behaviors.
Neural activity plays a major role in the development of sensory circuits in the mammalian brain. To date, there has been no direct test of whether taste-elicited neural activity has a role in shaping central gustatory circuits. However, recently developed genetic tools now allow an assessment of how specific taste stimuli, in this case sodium salt taste, play a role in the maturation of the terminal fields in the mouse brainstem. We found that the specific deletion of sodium salt taste during development produced terminal fields in adults that were dramatically larger than in control mice, demonstrating for the first time that sodium salt taste-elicited activity is necessary for the normal maturation of gustatory inputs into the brain.
神经元活动在哺乳动物大脑感觉回路的发育中起关键作用。在味觉系统中,现在可以通过对特定味觉转导过程进行基因操作来进行实验,以研究特定味觉特性(即基本味觉)如何影响味觉回路的功能和结构发育。在这里,我们使用了一种小鼠基因敲除模型,在整个发育过程中,味蕾细胞中用于区分钠盐与其他味觉刺激的转导成分被删除。我们使用这个模型来检验以下假设:钠盐味觉引发的活动缺失会影响将味觉信息从味蕾传递到延髓孤束核(NST)的神经终末场组织。标记舌咽神经、鼓索神经和岩大浅神经,以检查成年对照小鼠和味蕾中上皮钠通道α亚基被条件性删除的成年小鼠(αENaC基因敲除小鼠)的终末场。与对照小鼠各自的场体积相比,αENaC基因敲除小鼠中所有三条神经在NST中的终末场大2.7倍。两组之间场的形状相似;然而,αENaC基因敲除小鼠中标记的密度和分布更大。总体而言,我们的结果表明,传入的钠盐味觉信号中断会破坏所有终末场正常的年龄依赖性“修剪”,这可能导致感觉编码和味觉相关行为的改变。
神经活动在哺乳动物大脑感觉回路的发育中起主要作用。迄今为止,尚未直接测试味觉引发的神经活动是否在塑造中枢味觉回路中起作用。然而,最近开发的基因工具现在允许评估特定味觉刺激,在这种情况下是钠盐味觉,如何在小鼠脑干终末场的成熟中发挥作用。我们发现,发育过程中钠盐味觉的特异性缺失导致成年小鼠的终末场比对照小鼠大得多,首次证明钠盐味觉引发的活动对于味觉输入进入大脑的正常成熟是必要的。