首页> 外文期刊>American journal of rhinology & allergy >Sinonasal solitary chemosensory cells 'taste' the upper respiratory environment to regulate innate immunity
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Sinonasal solitary chemosensory cells 'taste' the upper respiratory environment to regulate innate immunity

机译:鼻腔孤立的化学感觉细胞“品尝”上呼吸道环境以调节先天免疫

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Results: Human sinonasal SCCs express both bitter T2R and sweet T1R2/3 receptors. Activation of SCC T2Rs activates a calcium signal that propagates to the surrounding epithelial cells and causes secretion of antimicrobial peptides. T1R2/3 sweet receptor activation by physiological airway surface liquid (ASL) glucose concentrations attenuates the T2R response, likely as a mechanism to prevent full activation of the T2R pathway except during times of infection, when pathogens may consume ASL glucose and reduce its concentration.Conclusion: SCCs appear to be important mediators of upper airway innate immunity, as the SCC T2Rs regulate antimicrobial peptide secretion, but further study is needed to determine the specific T2R isoforms involved as well as whether polymorphisms in these isoforms affect susceptibility to infection or patient outcomes in CRS. The inhibitory role of T1R2/3 sweet receptor suggests that T1R2/3 blockers may have therapeutic potential in some CRS patients, particularly those with diabetes mellitus. However, further clinical study of the relationship between infection and T1R2/3 genotype is required.Background: It is not fully understood how sinonasal epithelial cells detect the presence of pathogens and activate innate defense responses necessary for protecting the upper airway from infection. One mechanism is through bitter taste receptors (T2Rs), which are expressed in the sinonasal cavity. One T2R isoform, T2R38, is expressed in ciliated cells and detects quorum-sensing molecules from gram-negative bacteria, activating antimicrobial nitric oxide production. More recent studies have examined the role of T2Rs expressed in a sinonasal cell type that has only recently been identified in humans, the solitary chemosensory cell (SCC). We sought to provide an overview of SCCs and taste receptor function in human sinonasal defense as well as implications for chronic rhinosinusitis (CRS).Methods: A literature review of the current knowledge of SCCs and taste receptors in sinonasal physiology and CRS was conducted.
机译:结果:人鼻鼻窦鳞癌同时表达苦味T2R和甜味T1R2 / 3受体。 SCC T2Rs的激活激活了钙信号,该信号传播到周围的上皮细胞并引起抗菌肽的分泌。生理气道表面液(ASL)葡萄糖浓度激活的T1R2 / 3甜味受体会减弱T2R反应,这可能是一种防止T2R途径完全激活的机制,除非在感染期间,病原体可能会消耗ASL葡萄糖并降低其浓度。结论:SCC似乎是上呼吸道先天免疫的重要介体,因为SCC T2R调节抗菌肽的分泌,但是还需要进一步研究以确定所涉及的特定T2R亚型,以及这些亚型中的多态性是否会影响对感染或患者预后的敏感性在CRS中。 T1R2 / 3甜味受体的抑制作用表明,T1R2 / 3受体阻滞剂可能对某些CRS患者,特别是糖尿病患者具有治疗潜力。然而,还需要对感染与T1R2 / 3基因型之间的关系进行进一步的临床研究。背景:目前尚不完全了解鼻窦上皮细胞如何检测病原体并激活保护上呼吸道免受感染所必需的先天防御反应。一种机制是通过在鼻窦腔中表达的苦味受体(T2Rs)。一种T2R异构体T2R38在纤毛细胞中表达,可检测革兰氏阴性细菌的群体感应分子,从而激活抗菌一氧化氮的产生。最近的研究已经检查了在鼻窦细胞类型中表达的T2Rs的作用,这种类型的鼻窦细胞直到最近才在人类中被发现,即孤独的化学感觉细胞(SCC)。我们试图提供SCC和味觉受体在人鼻鼻窦防御中的功能以及对慢性鼻-鼻窦炎(CRS)的影响。方法:对SCC和味觉受体在鼻窦生理学和CRS中的最新知识进行了文献综述。

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