Huang Anthony Y, Wu Sandy Y
Department of Anatomy and Center for Integrated Research in Cognitive and Neural Science, Southern Illinois University School of Medicine, Carbondale, Illinois 62901
Department of Anatomy and.
J Neurosci. 2015 Sep 16;35(37):12714-24. doi: 10.1523/JNEUROSCI.0100-15.2015.
Immunoelectron microscopy revealed that peripheral afferent nerve fibers innervating taste buds contain calcitonin gene-related peptide (CGRP), which may be as an efferent transmitter released from peripheral axon terminals. In this report, we determined the targets of CGRP within taste buds and studied what effect CGRP exerts on taste bud function. We isolated mouse taste buds and taste cells, conducted functional imaging using Fura-2, and used cellular biosensors to monitor taste-evoked transmitter release. The findings showed that a subset of Presynaptic (Type III) taste cells (53%) responded to 0.1 μm CGRP with an increase in intracellular Ca(2+). In contrast, Receptor (Type II) taste cells rarely (4%) responded to 0.1 μm CGRP. Using pharmacological tools, the actions of CGRP were probed and elucidated by the CGRP receptor antagonist CGRP(8-37). We demonstrated that this effect of CGRP was dependent on phospholipase C activation and was prevented by the inhibitor U73122. Moreover, applying CGRP caused taste buds to secrete serotonin (5-HT), a Presynaptic (Type III) cell transmitter, but not ATP, a Receptor (Type II) cell transmitter. Further, our previous studies showed that 5-HT released from Presynaptic (Type III) cells provides negative paracrine feedback onto Receptor (Type II) cells by activating 5-HT1A receptors, and reducing ATP secretion. Our data showed that CGRP-evoked 5-HT release reduced taste-evoked ATP secretion. The findings are consistent with a role for CGRP as an inhibitory transmitter that shapes peripheral taste signals via serotonergic signaling during processing gustatory information in taste buds.
The taste sensation is initiated with a highly complex set of interactions between a variety of cells located within the taste buds before signal propagation to the brain. Afferent signals from the oral cavity are carried to the brain in chemosensory fibers that contribute to chemesthesis, the general chemical sensitivity of the mucus membranes in the oronasal cavities and being perceived as pungency, irritation, or heat. This is a study of a fundamental question in neurobiology: how are signals processed in sensory end organs, taste buds? More specifically, taste-modifying interactions, via transmitters, between gustatory and chemosensory afferents inside taste buds will help explain how a coherent output is formed before being transmitted to the brain.
免疫电子显微镜显示,支配味蕾的外周传入神经纤维含有降钙素基因相关肽(CGRP),其可能作为从外周轴突终末释放的传出递质。在本报告中,我们确定了味蕾内CGRP的作用靶点,并研究了CGRP对味蕾功能的影响。我们分离了小鼠味蕾和味细胞,使用Fura-2进行功能成像,并使用细胞生物传感器监测味觉诱发的递质释放。研究结果表明,一部分突触前(III型)味细胞(53%)对0.1μm CGRP有反应,细胞内Ca²⁺增加。相比之下,受体(II型)味细胞很少(4%)对0.1μm CGRP有反应。使用药理学工具,通过CGRP受体拮抗剂CGRP(8-37)探究并阐明了CGRP的作用。我们证明CGRP的这种作用依赖于磷脂酶C的激活,并被抑制剂U73122阻断。此外,应用CGRP会使味蕾分泌5-羟色胺(5-HT),一种突触前(III型)细胞递质,但不会分泌ATP,一种受体(II型)细胞递质。此外,我们之前的研究表明,从突触前(III型)细胞释放的5-HT通过激活5-HT1A受体并减少ATP分泌,对受体(II型)细胞提供负旁分泌反馈。我们的数据表明,CGRP诱发的5-HT释放减少了味觉诱发的ATP分泌。这些发现与CGRP作为一种抑制性递质的作用一致,即在味蕾处理味觉信息过程中,通过5-羟色胺能信号传导塑造外周味觉信号。
味觉感受始于味蕾内多种细胞之间一系列高度复杂的相互作用,然后信号才会传播到大脑。来自口腔的传入信号通过化学感觉纤维传递到大脑,这些纤维有助于化学感觉,即口鼻腔内黏膜的一般化学敏感性,表现为辛辣、刺激或热感。这是一项关于神经生物学基本问题的研究:信号在感觉终末器官味蕾中是如何处理的?更具体地说,味蕾内味觉和化学感觉传入神经之间通过递质进行的味觉调节相互作用,将有助于解释在信号传递到大脑之前如何形成连贯的输出。