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S-亚硝基谷胱甘肽诱导气道上皮细胞中功能性DeltaF508-囊性纤维化跨膜传导调节因子的产生。

S-Nitrosoglutathione induces functional DeltaF508-CFTR in airway epithelial cells.

作者信息

Andersson Charlotte, Gaston Benjamin, Roomans Godfried M

机构信息

Department of Medical Cell Biology, Uppsala University, Box 571, SE-75123 Uppsala, Sweden.

出版信息

Biochem Biophys Res Commun. 2002 Sep 27;297(3):552-7. doi: 10.1016/s0006-291x(02)02245-3.

Abstract

S-Nitrosoglutathione (GSNO) is an endogenous bronchodilator levels of which are reduced in the airways of cystic fibrosis (CF) patients. GSNO has recently been shown to increase maturation of CFTR in CF cell lines at physiological concentrations. The ability of S-nitrosoglutathione to direct the DeltaF508-CFTR to the plasma membrane and restore the function of the cAMP-dependent chloride transport in cultured human airway epithelial cells has been studied. Immunocytochemistry showed a time- and dose-dependent increase of apically located CFTR after GSNO treatment. Chloride transport studies with the fluorescent dye N-(ethoxycarbonylmethyl)-6-methoxyquinolinium bromide (MQAE) showed that GSNO was able to induce a fourfold increase of cAMP-dependent chloride transport. Our data and the fact that endogenous GSNO levels are lower in the airways of CF patients make GSNO an interesting candidate for pharmacological treatment of cystic fibrosis.

摘要

S-亚硝基谷胱甘肽(GSNO)是一种内源性支气管扩张剂,在囊性纤维化(CF)患者的气道中其水平会降低。最近研究表明,GSNO在生理浓度下可促进CF细胞系中CFTR的成熟。研究了S-亚硝基谷胱甘肽将DeltaF508-CFTR引导至质膜并恢复培养的人气道上皮细胞中cAMP依赖性氯离子转运功能的能力。免疫细胞化学显示,GSNO处理后,顶端定位的CFTR呈时间和剂量依赖性增加。用荧光染料N-(乙氧羰基甲基)-6-甲氧基喹啉溴化物(MQAE)进行的氯离子转运研究表明,GSNO能够使cAMP依赖性氯离子转运增加四倍。我们的数据以及CF患者气道中内源性GSNO水平较低这一事实,使得GSNO成为囊性纤维化药物治疗的一个有吸引力的候选药物。

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