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原发性纤毛运动障碍中鼻一氧化氮和一氧化氮合酶的表达。

Nasal nitric oxide and nitric oxide synthase expression in primary ciliary dyskinesia.

机构信息

Dept of Pediatrics, University of Pisa, Via Roma 67, 56126 Pisa, Italy.

出版信息

Eur Respir J. 2011 Mar;37(3):572-7. doi: 10.1183/09031936.00044310. Epub 2011 Jan 27.

DOI:10.1183/09031936.00044310
PMID:21273388
Abstract

No study has evaluated the correlation between different expression of nitric oxide synthase (NOS) isoforms in nasal epithelial cells and nasal NO (nNO) level in primary ciliary dyskinesia (PCD). Gene expression of endothelial (NOS3) and inducible NOS (NOS2) and their correlation with nNO level, ciliary function and morphology were studied in patients with PCD or secondary ciliary dyskinesia (SCD). NOS3 gene polymorphisms were studied in blood leukocytes. A total of 212 subjects were studied (48 with PCD, 161 with SCD and three normal subjects). nNO level correlated with mean ciliary beat frequency (p = 0.044; r = 0.174). The lower the nNO level the higher was the percentage of immotile cilia (p<0.001; r = -0.375). A significant positive correlation between NOS2 gene expression and nNO levels was demonstrated in all children (p = 0.001; r = 0.428), and this correlation was confirmed in patients with PCD (p = 0.019; r = 0.484). NOS2 gene expression was lower in PCD than in SCD (p = 0.04). The NOS3 isoform correlated with missing central microtubules (p = 0.048; r = 0.447). nNO levels were higher in PCD subjects with the NOS3 thymidine 894 mutation, and this was associated with a higher ciliary beat frequency (p = 0.045). These results demonstrate a relationship between nNO level, NOS mRNA expression and ciliary beat frequency.

摘要

尚无研究评估原发性纤毛运动障碍(PCD)患者鼻上皮细胞中不同一氧化氮合酶(NOS)同工型的表达与鼻一氧化氮(nNO)水平之间的相关性。本研究检测了 PCD 或继发性纤毛运动障碍(SCD)患者中内皮型(NOS3)和诱导型 NOS(NOS2)的基因表达,并研究其与 nNO 水平、纤毛功能和形态的相关性。还检测了血液白细胞中的 NOS3 基因多态性。共研究了 212 例受试者(48 例 PCD、161 例 SCD 和 3 例正常受试者)。nNO 水平与平均纤毛摆动频率相关(p = 0.044;r = 0.174)。nNO 水平越低,不动纤毛的比例越高(p<0.001;r = -0.375)。所有儿童均显示 NOS2 基因表达与 nNO 水平呈显著正相关(p = 0.001;r = 0.428),并且在 PCD 患者中也证实了这种相关性(p = 0.019;r = 0.484)。PCD 患者的 NOS2 基因表达低于 SCD(p = 0.04)。NOS3 同工型与中心微管缺失相关(p = 0.048;r = 0.447)。NOS3 胸腺嘧啶 894 突变的 PCD 患者 nNO 水平较高,并且与较高的纤毛摆动频率相关(p = 0.045)。这些结果表明 nNO 水平、NOS mRNA 表达与纤毛摆动频率之间存在相关性。

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