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T2R 介导的宿主-微生物相互作用的药理学。

Pharmacology of T2R Mediated Host-Microbe Interactions.

机构信息

Manitoba Chemosensory Biology Research Group, Department of Oral Biology, Dr. Gerald Niznick College of Dentistry, University of Manitoba, Winnipeg, MB, Canada.

Children's Hospital Research Institute of Manitoba, Winnipeg, MB, Canada.

出版信息

Handb Exp Pharmacol. 2022;275:177-202. doi: 10.1007/164_2021_435.

Abstract

Bitter taste receptors (T2Rs) belong to the G protein-coupled receptor superfamily. Humans express 25 T2Rs that are known to detect several bitter compounds including bacterial quorum sensing molecules (QSM). Primarily found to be key receptors for bitter sensation T2Rs are known to play an important role in mediating innate immune responses in oral and extraoral tissues. Several studies have led to identification of Gram-negative and Gram-positive bacterial QSMs as agonists for T2Rs in airway epithelial cells and immune cells. However, the pharmacological characterization for many of the QSM-T2R interactions remains poorly defined. In this chapter, we discuss the extraoral roles including localization of T2Rs in extracellular vesicles, molecular pharmacology of QSM-T2R interactions, role of T2Rs in mediating innate immune responses, and some of the challenges in understanding T2R pharmacology.

摘要

苦味受体(T2R)属于 G 蛋白偶联受体超家族。人类表达 25 种 T2R,已知它们可以检测到包括细菌群体感应分子(QSM)在内的几种苦味化合物。T2R 主要被认为是苦味感知的关键受体,已知它们在口腔和口腔外组织中的先天免疫反应中发挥重要作用。几项研究已经确定革兰氏阴性和革兰氏阳性细菌的 QSM 是气道上皮细胞和免疫细胞中 T2R 的激动剂。然而,许多 QSM-T2R 相互作用的药理学特征仍未得到很好的定义。在本章中,我们讨论了 T2R 在细胞外囊泡中的定位等口腔外作用、QSM-T2R 相互作用的分子药理学、T2R 在介导先天免疫反应中的作用以及理解 T2R 药理学的一些挑战。

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