Hariri Benjamin M, Payne Sakeena J, Chen Bei, Mansfield Corrine, Doghramji Laurel J, Adappa Nithin D, Palmer James N, Kennedy David W, Niv Masha Y, Lee Robert J
department of Otorhinolaryngology-Head and Neck Surgery, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
Am J Rhinol Allergy. 2016 Jul;30(4):261-8. doi: 10.2500/ajra.2016.30.4331.
T2R bitter taste receptors play a crucial role in sinonasal innate immunity by upregulating mucociliary clearance and nitric oxide (NO) production in response to bitter gram-negative quorum-sensing molecules in the airway surface liquid. Previous studies showed that phytochemical flavonoid metabolites, known as anthocyanidins, taste bitter and have antibacterial effects. Our objectives were to examine the effects of anthocyanidins on NO production by human sinonasal epithelial cells and ciliary beat frequency, and their impact on common sinonasal pathogens Pseudomonas aeruginosa and Staphylococcus aureus.
Ciliary beat frequency and NO production were measured by using digital imaging of differentiated air-liquid interface cultures prepared from primary human cells isolated from residual surgical material. Plate-based assays were used to determine the effects of anthocyanidins on bacterial swimming and swarming motility. Biofilm formation and planktonic growth were also assessed.
Anthocyanidin compounds triggered epithelial cells to produce NO but not through T2R receptors. However, anthocyanidins did not impact ciliary beat frequency. Furthermore, they did not reduce biofilm formation or planktonic growth of P. aeruginosa. In S. aureus, they did not reduce planktonic growth, and only one compound had minimal antibiofilm effects. The anthocyanidin delphinidin and anthocyanin keracyanin were found to promote bacterial swimming, whereas anthocyanidin cyanidin and flavonoid myricetin did not. No compounds that were tested inhibited bacterial swarming.
Results of this study indicated that, although anthocyanidins may elicited an innate immune NO response from human cells, they do not cause an increase in ciliary beating and they may also cause a pathogenicity-enhancing effect in P. aeruginosa. Additional studies are necessary to understand how this would affect the use of anthocyanidins as therapeutics. This study emphasized the usefulness of in vitro screening of candidate compounds against multiple parameters of both epithelial and bacterial physiologies to prioritize candidates for in vivo therapeutic testing.
T2R苦味受体通过上调黏液纤毛清除功能以及在气道表面液体中对革兰氏阴性菌群体感应分子产生反应时一氧化氮(NO)的生成,在鼻窦先天免疫中发挥关键作用。先前的研究表明,植物化学类黄酮代谢产物,即花青素,味道苦涩且具有抗菌作用。我们的目标是研究花青素对人鼻窦上皮细胞产生NO以及纤毛摆动频率的影响,及其对常见鼻窦病原体铜绿假单胞菌和金黄色葡萄球菌的作用。
使用从手术剩余材料中分离的原代人细胞制备的分化气液界面培养物的数字成像来测量纤毛摆动频率和NO生成。基于平板的试验用于确定花青素对细菌游动和群体运动的影响。还评估了生物膜形成和浮游生长情况。
花青素化合物可触发上皮细胞产生NO,但并非通过T2R受体。然而,花青素并未影响纤毛摆动频率。此外,它们并未减少铜绿假单胞菌的生物膜形成或浮游生长。在金黄色葡萄球菌中,它们并未减少浮游生长,只有一种化合物具有最小的抗生物膜作用。发现花青素飞燕草素和花青素矢车菊素可促进细菌游动,而花青素花青素和类黄酮杨梅素则不能。所测试的化合物均未抑制细菌群体运动。
本研究结果表明,尽管花青素可能会引发人细胞的先天免疫NO反应,但它们不会导致纤毛摆动增加,并且它们还可能对铜绿假单胞菌产生致病性增强作用。需要进一步研究以了解这将如何影响花青素作为治疗药物的使用。本研究强调了针对上皮和细菌生理学的多个参数对候选化合物进行体外筛选以确定体内治疗测试候选物优先级的有用性。