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利用小鼠基因组编辑进行表位标记研究发现,质子通道OTOP1定位于顶端,并非仅存在于III型“酸味”味觉感受器细胞中。

Epitope Tagging with Genome Editing in Mice Reveals That the Proton Channel OTOP1 Is Apically Localized and Not Restricted to Type III "Sour" Taste Receptor Cells.

作者信息

Kaplan Joshua P, Ye Wenlei, Kileen Heather, Liang Ziyu, Tran Anne, Chi Jingyi, Yang Chingwen, Cohen Paul, Liman Emily R

机构信息

Section of Neurobiology, Department of Biological Sciences, University of Southern California, Los Angeles, California 90089.

Program in Neuroscience, University of Southern California, Los Angeles, California 90089.

出版信息

J Neurosci. 2025 Feb 5;45(6):e1560242024. doi: 10.1523/JNEUROSCI.1560-24.2024.

Abstract

The gustatory system allows animals to assess the nutritive value and safety of foods prior to ingestion. The first step in gustation is the interaction of taste stimuli with one or more specific sensory receptors that are generally believed to be present on the apical surface of the taste receptor cells. However, this assertion is rarely tested. We recently identified OTOP1 as a proton channel and showed that it is required for taste response to acids (sour) and ammonium. Here, we examined the cellular and subcellular localization of OTOP1 by tagging the endogenous OTOP1 protein with an N-terminal HA epitope (HA-OTOP1). Using both male and female HA-OTOP1 mice and high-resolution imaging, we show that OTOP1 is strictly localized to the apical tips of taste cells throughout the tongue and oral cavity. Interestingly, immunoreactivity is observed in the actin-rich taste pore above the tight junctions defined by zonula occludens-1 (ZO-1) and also immediately below these junctions. Surprisingly, OTOP1 immunoreactivity is not restricted to Type III taste receptor cells (TRCs) that mediate sour taste but is also observed in glia-like Type I TRCs proposed to perform housekeeping functions, a result that is corroborated by scRNA-seq data. The apical localization of OTOP1 supports the contention that OTOP1 functions as a taste receptor and suggests that OTOP1 may be accessible to orally available compounds that could act as taste modifiers.

摘要

味觉系统使动物在摄入食物之前能够评估食物的营养价值和安全性。味觉的第一步是味觉刺激与一种或多种特定的感觉受体相互作用,这些受体通常被认为存在于味觉受体细胞的顶端表面。然而,这一论断很少得到验证。我们最近将OTOP1鉴定为一种质子通道,并表明它是对酸(酸味)和铵产生味觉反应所必需的。在这里,我们通过用N端HA表位(HA-OTOP1)标记内源性OTOP1蛋白,研究了OTOP1的细胞和亚细胞定位。利用雄性和雌性HA-OTOP1小鼠以及高分辨率成像技术,我们发现OTOP1严格定位于整个舌头和口腔中味觉细胞的顶端。有趣的是,在由紧密连接蛋白-1(ZO-1)定义的紧密连接上方富含肌动蛋白的味觉孔中以及这些连接下方紧邻处均观察到免疫反应性。令人惊讶的是,OTOP1免疫反应性并不局限于介导酸味的III型味觉受体细胞(TRC),在被认为执行管家功能的胶质样I型TRC中也观察到了这种反应,这一结果得到了单细胞RNA测序数据的证实。OTOP1的顶端定位支持了OTOP1作为味觉受体发挥作用的观点,并表明OTOP1可能可被作为味觉调节剂的口服可用化合物所接触到。

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