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本文引用的文献

1
Bitter taste receptor T2R38 is expressed on skin-infiltrating lymphocytes and regulates lymphocyte migration.苦味受体 T2R38 表达在皮肤浸润淋巴细胞上,并调节淋巴细胞迁移。
Sci Rep. 2022 Jul 11;12(1):11790. doi: 10.1038/s41598-022-15999-6.
2
Bitter Taste Receptor Expression in Chronic Rhinosinusitis with Nasal Polyps: New Data on Polypoid Tissue.慢性鼻-鼻窦炎伴鼻息肉中苦味受体的表达:息肉组织的新数据。
Int J Mol Sci. 2022 Jul 1;23(13):7345. doi: 10.3390/ijms23137345.
3
Bitter taste signaling in tracheal epithelial brush cells elicits innate immune responses to bacterial infection.气管上皮刷状细胞的苦味信号转导引发针对细菌感染的固有免疫反应。
J Clin Invest. 2022 Jul 1;132(13). doi: 10.1172/JCI150951.
4
Intestinal Tuft-2 cells exert antimicrobial immunity via sensing bacterial metabolite N-undecanoylglycine.肠道簇绒2细胞通过感知细菌代谢产物N-十一烷酰甘氨酸发挥抗菌免疫作用。
Immunity. 2022 Apr 12;55(4):686-700.e7. doi: 10.1016/j.immuni.2022.03.001. Epub 2022 Mar 22.
5
The preference for sugar over sweetener depends on a gut sensor cell.对糖而非甜味剂的偏好取决于一种肠道传感细胞。
Nat Neurosci. 2022 Feb;25(2):191-200. doi: 10.1038/s41593-021-00982-7. Epub 2022 Jan 13.
6
Whole-Brain Mapping of the Expression Pattern of , a Subunit Specific to the Sweet Taste Receptor.甜味受体特异性亚基α-味导素表达模式的全脑图谱。 (注:原文中“of”后面似乎缺失了具体内容,这里根据常见语境补充了“α-gustducin”,你可根据实际情况调整)
Front Neuroanat. 2021 Oct 28;15:751839. doi: 10.3389/fnana.2021.751839. eCollection 2021.
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SCLC Subtypes Defined by ASCL1, NEUROD1, POU2F3, and YAP1: A Comprehensive Immunohistochemical and Histopathologic Characterization.SCLC 亚型的定义:ASCL1、NEUROD1、POU2F3 和 YAP1:全面的免疫组化和组织病理学特征。
J Thorac Oncol. 2020 Dec;15(12):1823-1835. doi: 10.1016/j.jtho.2020.09.009. Epub 2020 Oct 1.
8
Cell fate specification and differentiation in the adult mammalian intestine.成年哺乳动物肠道中的细胞命运特化和分化。
Nat Rev Mol Cell Biol. 2021 Jan;22(1):39-53. doi: 10.1038/s41580-020-0278-0. Epub 2020 Sep 21.
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The gut-brain axis mediates sugar preference.肠道-大脑轴介导糖偏好。
Nature. 2020 Apr;580(7804):511-516. doi: 10.1038/s41586-020-2199-7. Epub 2020 Apr 15.
10
Bitter taste receptors stimulate phagocytosis in human macrophages through calcium, nitric oxide, and cyclic-GMP signaling.苦味受体通过钙、一氧化氮和环鸟苷酸信号刺激人巨噬细胞的吞噬作用。
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味蕾之外的味觉感受器。

Taste Receptors beyond Taste Buds.

机构信息

Department of Pharmacology, Korea University College of Medicine, Seoul 02841, Korea.

BK21 Graduate Program, Department of Biomedical Sciences, Korea University College of Medicine, Seoul 02841, Korea.

出版信息

Int J Mol Sci. 2022 Aug 26;23(17):9677. doi: 10.3390/ijms23179677.

DOI:10.3390/ijms23179677
PMID:36077074
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9455917/
Abstract

Taste receptors are responsible for detecting their ligands not only in taste receptor cells (TRCs) but also in non-gustatory organs. For several decades, many research groups have accumulated evidence for such "ectopic" expression of taste receptors. More recently, some of the physiologic functions (apart from taste) of these ectopic taste receptors have been identified. Here, we summarize our current understanding of these ectopic taste receptors across multiple organs. With a particular focus on the specialized epithelial cells called tuft cells, which are now considered siblings of type II TRCs, we divide the ectopic expression of taste receptors into two categories: taste receptors in TRC-like cells outside taste buds and taste receptors with surprising ectopic expression in completely different cell types.

摘要

味觉受体不仅在味觉受体细胞(TRC)中,而且在非味觉器官中负责检测其配体。几十年来,许多研究小组积累了这些“异位”表达味觉受体的证据。最近,这些异位味觉受体的一些生理功能(味觉除外)已经被确定。在这里,我们总结了我们目前对多个器官中这些异位味觉受体的理解。特别关注一种称为绒毛细胞的特化上皮细胞,它们现在被认为是 II 型 TRC 的兄弟姐妹,我们将味觉受体的异位表达分为两类:味蕾外的 TRC 样细胞中的味觉受体和在完全不同细胞类型中具有惊人异位表达的味觉受体。