Suppr超能文献

与系统性硬化症相关肺动脉高压易感性相关的NOS2基因多态性:对转录活性的影响

NOS2 polymorphisms associated with the susceptibility to pulmonary arterial hypertension with systemic sclerosis: contribution to the transcriptional activity.

作者信息

Kawaguchi Yasushi, Tochimoto Akiko, Hara Masako, Kawamoto Manabu, Sugiura Tomoko, Katsumata Yasuhiro, Okada Jun, Kondo Hirobumi, Okubo Mitsuo, Kamatani Naoyuki

机构信息

Institute of Rheumatology, Tokyo Women's Medical University, Tokyo, Japan.

出版信息

Arthritis Res Ther. 2006;8(4):R104. doi: 10.1186/ar1984.

Abstract

Systemic sclerosis (SSc) is a connective tissue disease characterized by tissue fibrosis. One of several complications of SSc, pulmonary arterial hypertension (PAH) can be refractory to treatment, both novel and established. In the present study we investigated the ratio of circulating nitric oxide to endothelin-1 in patients with both SSc and PAH, and determined whether polymorphisms in NOS2 (the nitric oxide synthase 2 gene) are associated with susceptibility to PAH. Endothelin-1 in plasma and nitric oxide metabolites (nitrate and nitrite) in serum were measured. The nitric oxide/endothelin-1 ratio was significantly lower in patients with both SSc and PAH than in patients with SSc only or in healthy control individuals. We confirmed the presence of two single nucleotide polymorphisms at positions -1,026 and -277 and a pentanucleotide repeat (CCTTT) at -2.5 kilobases. There were significant differences in single nucleotide polymorphisms between patients with SSc who had PAH and those who did not, and between patients with both SSc and PAH and healthy control individuals. The CCTTT repeat was significantly shorter in patients with both SSc and PAH than in patients with SSc only or in healthy control individuals. Transcriptional activity were analyzed using the luciferase reporter assay. The transcriptional activity of NOS2 was much greater in fibroblasts transfected by a vector with a long allele of the CCTTT repeat than in those transfected by a vector with a short allele. Polymorphisms in the NOS2 gene are associated with transcriptional activity of the NOS2 gene and with susceptibility to SSc-related PAH.

摘要

系统性硬化症(SSc)是一种以组织纤维化为特征的结缔组织疾病。肺动脉高压(PAH)是SSc的几种并发症之一,无论是新型治疗还是已有的治疗方法,对其治疗都可能无效。在本研究中,我们调查了患有SSc和PAH的患者循环一氧化氮与内皮素-1的比例,并确定一氧化氮合酶2基因(NOS2)中的多态性是否与PAH易感性相关。我们测量了血浆中的内皮素-1和血清中的一氧化氮代谢产物(硝酸盐和亚硝酸盐)。同时患有SSc和PAH的患者的一氧化氮/内皮素-1比例显著低于仅患有SSc的患者或健康对照个体。我们确认了在-1026和-277位置存在两个单核苷酸多态性,以及在-2.5千碱基处存在一个五核苷酸重复序列(CCTTT)。患有PAH的SSc患者与未患PAH的SSc患者之间,以及同时患有SSc和PAH的患者与健康对照个体之间,单核苷酸多态性存在显著差异。同时患有SSc和PAH的患者的CCTTT重复序列明显短于仅患有SSc的患者或健康对照个体。使用荧光素酶报告基因检测分析转录活性。用具有CCTTT重复序列长等位基因的载体转染的成纤维细胞中,NOS2的转录活性比用具有短等位基因的载体转染的成纤维细胞中的转录活性高得多。NOS2基因中的多态性与NOS2基因的转录活性以及SSc相关PAH的易感性相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d52d/1779390/129ff11d43a1/ar1984-1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验