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诱导型一氧化氮合酶的表达及移植后闭塞性细支气管炎中过氧亚硝酸盐的形成

Expression of inducible nitric oxide synthase and formation of peroxynitrite in posttransplant obliterative bronchiolitis.

作者信息

Mason N A, Springall D R, Pomerance A, Evans T J, Yacoub M H, Polak J M

机构信息

Department of Histochemistry, Royal Postgraduate Medical School, London, United Kingdom.

出版信息

J Heart Lung Transplant. 1998 Jul;17(7):710-4.

PMID:9703237
Abstract

BACKGROUND

Obliterative bronchiolitis is characterized histologically by inflammation, epithelial cell damage and loss, fibrosis, and eventual obliteration of airways. Production of high levels of the potential cytotoxin nitric oxide by inducible nitric oxide synthase has been implicated in several inflammatory diseases. The damaging effects of nitric oxide are mediated by peroxynitrite, are formed from nitric oxide and superoxide, and can be demonstrated by the detection of nitrotyrosine. Our previous finding of high inducible nitric oxide synthase expression in inflamed airway epithelium led us to hypothesize that release of nitric oxide in obliterative bronchiolitis mediates the characteristic epithelial damage.

METHODS

Immunocytochemistry was carried out to seek expression of inducible nitric oxide synthase and nitrotyrosine in transplant samples from patients with obliterative bronchiolitis (n=10) and, as controls, unused donor lungs (n=5).

RESULTS

Inducible nitric oxide synthase was strongly expressed in the damaged airway epithelium in obliterative bronchiolitis and in inflammatory cells, where its distribution was matched by that of nitrotyrosine. Normal controls showed little or no immunoreactivity for any of the antigens studied.

CONCLUSIONS

Our findings suggest that nitric oxide may play a role in the pathogenesis of obliterative bronchiolitis and indicate that further work is essential to fully understand the processes and mechanisms involved.

摘要

背景

闭塞性细支气管炎的组织学特征为炎症、上皮细胞损伤与丢失、纤维化以及最终气道闭塞。诱导型一氧化氮合酶产生高水平潜在细胞毒素一氧化氮,这与多种炎症性疾病有关。一氧化氮的损伤作用由过氧亚硝酸盐介导,过氧亚硝酸盐由一氧化氮和超氧化物形成,可通过检测硝基酪氨酸来证实。我们之前在炎症气道上皮中发现诱导型一氧化氮合酶高表达,这使我们推测闭塞性细支气管炎中一氧化氮的释放介导了特征性的上皮损伤。

方法

对闭塞性细支气管炎患者(n = 10)的移植样本以及作为对照的未使用的供体肺(n = 5)进行免疫细胞化学检测,以寻找诱导型一氧化氮合酶和硝基酪氨酸的表达。

结果

诱导型一氧化氮合酶在闭塞性细支气管炎受损气道上皮及炎症细胞中强烈表达,其分布与硝基酪氨酸的分布相匹配。正常对照对所研究的任何抗原几乎没有或没有免疫反应性。

结论

我们的研究结果表明一氧化氮可能在闭塞性细支气管炎的发病机制中起作用,并表明进一步的研究对于充分理解其中涉及的过程和机制至关重要。

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