NADPH氧化酶NOX1、NOX2和DUOX2在溃疡性结肠炎中的表达分析

doi:10.3969/j.issn.1006-7795.2017.02.014

首都医科大学学报 ›› 2017, Vol. 38 ›› Issue (2): 220-226.doi: 10.3969/j.issn.1006-7795.2017.02.014

NADPH氧化酶NOX1、NOX2和DUOX2在溃疡性结肠炎中的表达分析

轩青霞¹, 戴发亮¹, 陈攀¹, 冯丹丹¹, 金建军¹, 高强^1,2

1. 河南科技大学临床医学院, 河南科技大学第一附属医院消化内科, 河南洛阳 471023;
2. 首都医科大学附属北京康复医院消化内科, 北京 100144

收稿日期:2016-12-07 出版日期:2017-03-21 发布日期:2017-04-17
通讯作者: 高强,E-mail:gaoq@ccmu.edu.cn E-mail:gaoq@ccmu.edu.cn
基金资助:
国家自然科学基金（81370487）

Significance of NADPH oxidases NOX1, NOX2 and DUOX2 expression in inflammatory bowel disease

Xuan Qingxia¹, Dai Faliang¹, Chen Pan¹, Feng Dandan¹, Jin Jianjun¹, Gao Qiang^1,2

1. Department of Gastroenterology and Hepatology, The First Affiliated Hospital, and College of Clinical Medicine of Henan University of Science and Technology, Luoyang 471003, Henan Province, China;
2. Department of Gastroenterology and Hepatology, Beijing Rehabilitation Hospital, Capital Medical University, Beijing 100114, China

Received:2016-12-07 Online:2017-03-21 Published:2017-04-17
Supported by:
This study was supported by National Natural Science Foundation of China (81370487)

摘要/Abstract

摘要： 目的探讨NADPH氧化酶家族（nicotinamide adenine dinucleotide phosphate oxidases，NOXs）的主要成员NOX1、NOX2和双氧化物酶（dual oxidase，DUOX）2（人：NOX1、NOX2和DUOX2;小鼠：Nox1、Nox2 和Duox2）在人炎症性肠病和小鼠肠炎模型结肠中的表达。方法人结肠标本选自于通过结肠镜活检或手术切除的炎症性肠病组织及距离病变组织边缘5 cm以上正常组织; 同时选用8~10周龄的C57BL/6雌性小鼠建立结肠炎模型，采用掷硬币法将其随机分为对照组和慢性肠炎组，慢性肠炎组先自由饮用1.0%（质量分数）葡聚糖硫酸钠7 d，然后自由饮水14 d，循环3次;通过体质量变化和HE染色方法评估肠道炎性反应程度。采用实时定量PCR技术和免疫组织化学方法分别检测结肠组织中NOX1、NOX2及DUOX2 mRNA和蛋白表达情况，并分析在人炎症性肠病中三者表达情况与临床特征之间的关系。结果 NOX1、NOX2和DUOX2 mRNA在人炎症性肠病结肠组织中的表达量均显著高于自身正常对照组织，分别增高2.8、2.0和3.3倍（P均<0.01）;与人不同，Nox1和Duox2 mRNA在小鼠慢性肠炎结肠组织中的表达量差异无统计学意义，Nox2 mRNA增加2.4倍（P<0.01）。Nox1蛋白在正常结肠上皮细胞刷状缘和胞质中表达;Nox2蛋白主要表达于浸润的吞噬细胞和中性粒细胞;Duox2蛋白在正常结肠黏膜组织中低表达;三者在人炎症性肠病结肠组织中表达均上调（均P<0.01）;在小鼠慢性肠炎模型中，Nox2和Duox2蛋白上调（均P<0.01），而Nox1无变化。除了NOX2 mRNA在男性病人表达高于女性病人外，未发现这些氧化酶与病人临床特征之间有关联。结论 NOX1、NOX2和DUOX2不但在维持机体正常生理功能过程中发挥重要作用，而且在炎症性肠病初期阶段的发病中也起一定的作用。

关键词: NADPH氧化酶, NOX1, NOX2, DUOX2, 炎症性肠病

Abstract: Objective To investigate the expression of NOX1, NOX2 and DUOX2, the members of nicotinamide adenine dinucleotide phosphate (NADPH) oxidase family, in large intestine of patients with inflammatory bowel disease (IBD) and mouse colitis and analyze the relationship between these enzymes and IBD. Methods The samples were collected from large intestine of patients with IBD. Mouse chronic colitis model was established by using eight to ten-week-old C57BL/6 mice treated with three cycles of drinking 1.0% dextran sulfate sodium (DSS) for 7 days plus drinking water for 14 days. Mouse body weight change and hematoxylin-eosin (HE) staining of colon sections were used to evaluate the severity of inflammatory lesions. The expression of NOX1, NOX2 and DUOX2 gene and protein were detected by real-time quantitative reverse transcription polymerase chain reaction (RT-PCR) and immunohistochemistry, respectively. Results The expression of NOX1, NOX2 and DUOX2 mRNA significantly increased in human inflamed tissues compared to paired normal tissues (all P<0.01). NOX2 mRNA higher in male patients than female. Unlike human, only Nox2 mRNA increased by 2.4 times in chronic colitis mice, Nox1 and Duox2 mRNA remained unchanged. These three proteins in IBD patients increased (all P<0.01); in chronic colitis mice Nox2 and Duox2 proteins increased (both P<0.01), but Nox1 did not. Conclusion NOX1, NOX2 and DUOX2 not only play an important role in maintaining the normal physiological function, but also were associated with early onset IBD.

Key words: NADPH oxidases, NOX1, NOX2, DUOX2, inflammatory bowel disease (IBD)

中图分类号:

R574

轩青霞, 戴发亮, 陈攀, 冯丹丹, 金建军, 高强. NADPH氧化酶NOX1、NOX2和DUOX2在溃疡性结肠炎中的表达分析[J]. 首都医科大学学报, 2017, 38(2): 220-226.

Xuan Qingxia, Dai Faliang, Chen Pan, Feng Dandan, Jin Jianjun, Gao Qiang. Significance of NADPH oxidases NOX1, NOX2 and DUOX2 expression in inflammatory bowel disease[J]. Journal of Capital Medical University, 2017, 38(2): 220-226.

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NADPH氧化酶NOX1、NOX2和DUOX2在溃疡性结肠炎中的表达分析

Significance of NADPH oxidases NOX1, NOX2 and DUOX2 expression in inflammatory bowel disease

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