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碳酸氢盐、谷胱甘肽和抗坏血酸的新型疗法可改善囊性纤维化黏液转运。

Novel Therapy of Bicarbonate, Glutathione, and Ascorbic Acid Improves Cystic Fibrosis Mucus Transport.

机构信息

Cystic Fibrosis Research Center.

Department of Cellular, Developmental, and Integrative Biology.

出版信息

Am J Respir Cell Mol Biol. 2020 Sep;63(3):362-373. doi: 10.1165/rcmb.2019-0287OC.

Abstract

Defective airway mucus clearance is a defining characteristic of cystic fibrosis lung disease, and improvements to current mucolytic strategies are needed. Novel approaches targeting a range of contributing mechanisms are in various stages of preclinical and clinical development. ARINA-1 is a new nebulized product comprised of ascorbic acid, glutathione, and bicarbonate. Using microoptical coherence tomography, we tested the effect of ARINA-1 on central features of mucociliary clearance in F508del/F508del primary human bronchial epithelial cells to assess its potential as a mucoactive therapy in cystic fibrosis. We found that ARINA-1 significantly augmented mucociliary transport rates, both alone and with CFTR (cystic fibrosis transmembrane conductance regulator) modulator therapy, whereas airway hydration and ciliary beating were largely unchanged compared with PBS vehicle control. Analysis of mucus reflectivity and particle-tracking microrheology indicated that ARINA-1 restores mucus clearance by principally reducing mucus layer viscosity. The combination of bicarbonate and glutathione elicited increases in mucociliary transport rate comparable to those seen with ARINA-1, indicating the importance of this interaction to the impact of ARINA-1 on mucus transport; this effect was not recapitulated with bicarbonate alone or bicarbonate combined with ascorbic acid. Assessment of CFTR chloride transport revealed an increase in CFTR-mediated chloride secretion in response to ARINA-1 in CFBE41o cells expressing wild-type CFTR, driven by CFTR activity stimulation by ascorbate. This response was absent in CFBE41o F508del cells treated with VX-809 and primary human bronchial epithelial cells, implicating CFTR-independent mechanisms for the effect of ARINA-1 on cystic fibrosis mucus. Together, these studies indicate that ARINA-1 is a novel potential therapy for the treatment of impaired mucus clearance in cystic fibrosis.

摘要

气道黏液清除功能障碍是囊性纤维化肺部疾病的一个特征,需要改进目前的黏液溶解策略。针对一系列致病机制的新方法正在处于临床前和临床开发的各个阶段。ARINA-1 是一种新的雾化产品,由抗坏血酸、谷胱甘肽和碳酸氢盐组成。使用微光学相干断层扫描,我们测试了 ARINA-1 对 F508del/F508del 原发性人支气管上皮细胞中黏液纤毛清除的中心特征的影响,以评估其作为囊性纤维化中黏液活性治疗的潜力。我们发现,ARINA-1 单独使用和与 CFTR(囊性纤维化跨膜电导调节因子)调节剂治疗均可显著增加黏液纤毛转运速率,而与 PBS 载体对照相比,气道水合作用和纤毛搏动基本不变。对黏液反射率和粒子追踪微流变学的分析表明,ARINA-1 通过主要降低黏液层黏度来恢复黏液清除。碳酸氢盐和谷胱甘肽的组合引起的黏液纤毛转运速率增加与 ARINA-1 相似,表明这种相互作用对 ARINA-1 对黏液转运的影响很重要;单独使用碳酸氢盐或碳酸氢盐与抗坏血酸组合均未再现这种作用。对 CFTR 氯离子转运的评估显示,在表达野生型 CFTR 的 CFBE41o 细胞中,ARINA-1 引起 CFTR 介导的氯离子分泌增加,这是由抗坏血酸对 CFTR 活性的刺激驱动的。在用 VX-809 处理的 CFBE41o F508del 细胞和原代人支气管上皮细胞中未观察到这种反应,这表明 ARINA-1 对囊性纤维化黏液的作用涉及 CFTR 非依赖性机制。总之,这些研究表明,ARINA-1 是一种治疗囊性纤维化黏液清除障碍的新型潜在治疗方法。

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