4.7 Review

An update on extra-oral bitter taste receptors

期刊

JOURNAL OF TRANSLATIONAL MEDICINE
卷 19, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12967-021-03067-y

关键词

G-protein coupled receptors (GPCRs); Bitter taste-sensing type 2 receptors (TAS2Rs); TAS2R polymorphisms; Bitter compounds; Extraoral tissues; Innate immunity; Muscle contractility; Cancer

资金

  1. Medical University of Lublin

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TAS2Rs, crucial for bitterness perception, are not only found in taste bud cells but also in various extra-oral tissues, playing key roles in diverse physiological processes and diseases. Recent studies suggest the therapeutic potential of TAS2Rs as novel targets due to their selectivity and expression profiles.
Bitter taste-sensing type 2 receptors (TAS2Rs or T2Rs), belonging to the subgroup of family A G-protein coupled receptors (GPCRs), are of crucial importance in the perception of bitterness. Although in the first instance, TAS2Rs were considered to be exclusively distributed in the apical microvilli of taste bud cells, numerous studies have detected these sensory receptor proteins in several extra-oral tissues, such as in pancreatic or ovarian tissues, as well as in their corresponding malignancies. Critical points of extra-oral TAS2Rs biology, such as their structure, roles, signaling transduction pathways, extensive mutational polymorphism, and molecular evolution, have been currently broadly studied. The TAS2R cascade, for instance, has been recently considered to be a pivotal modulator of a number of (patho)physiological processes, including adipogenesis or carcinogenesis. The latest advances in taste receptor biology further raise the possibility of utilizing TAS2Rs as a therapeutic target or as an informative index to predict treatment responses in various disorders. Thus, the focus of this review is to provide an update on the expression and molecular basis of TAS2Rs functions in distinct extra-oral tissues in health and disease. We shall also discuss the therapeutic potential of novel TAS2Rs targets, which are appealing due to their ligand selectivity, expression pattern, or pharmacological profiles.

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