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肿瘤坏死因子在肺水肿中的双重作用。

The Dual Role of TNF in Pulmonary Edema.

作者信息

Yang Guang, Hamacher Jürg, Gorshkov Boris, White Richard, Sridhar Supriya, Verin Alexander, Chakraborty Trinad, Lucas Rudolf

机构信息

Vascular Biology Center & Department of Pharmacology and Toxicology, Medical College of Georgia, Augusta, GA, 30912, USA.

出版信息

J Cardiovasc Dis Res. 2010 Jan;1(1):29-36. doi: 10.4103/0975-3583.59983.

Abstract

UNLABELLED

-Pulmonary edema, a major manifestation of left ventricular heart failure, renal insufficiency, shock, diffuse alveolar damage and lung hypersensitivity states, is a significant medical problem worldwide and can be life-threatening. The proinflammatory cytokine tumor necrosis factor (TNF) has been shown to contribute to the pathogenesis and development of pulmonary edema. However, some recent studies have demonstrated surprisingly that TNF can also promote alveolar fluid reabsorption in vivo and in vitro. This protective effect of the cytokine is mediated by the lectin-like domain of the cytokine, which is spatially distinct from the TNF receptor binding sites. The TIP peptide, a synthetic mimic of the lectin-like domain of TNF, can significantly increase alveolar fluid clearance and improve lung compliance in pulmonary edema models. In this review, we will discuss the dual role of TNF in pulmonary edema.

ABBREVIATIONS

-tumor necrosis factor (TNF); acute lung injury (ALI); acute respiratory distress syndrome (ARDS); positive end-expiratory pressure (PEEP);epithelial sodium channel (ENaC);neural precursor cell-expressed developmentally downregulated (gene 4) protein (Nedd4-2);serum and glucocorticoid dependent kinase (Sgk-1);insulin-like growth factor 1 (IGF-1);Protein Kinase C (PKC);reactive oxygen species (ROS);myosin light chain (MLC);pneumolysin (PLY);listeriolysin (LLO);interleukin (IL);bronchoalveolar lavage fluids (BALF);Bacillus Calmette-Guerin (BCG);TNF receptor type 1 (TNFR1); TNF receptor type 2 (TNF-R2);

摘要

未标注

肺水肿是左心室心力衰竭、肾功能不全、休克、弥漫性肺泡损伤和肺超敏反应状态的主要表现,是全球范围内一个重大的医学问题,可能危及生命。促炎细胞因子肿瘤坏死因子(TNF)已被证明与肺水肿的发病机制和发展有关。然而,最近一些研究令人惊讶地表明,TNF在体内和体外也能促进肺泡液体重吸收。细胞因子的这种保护作用由细胞因子的凝集素样结构域介导,该结构域在空间上与TNF受体结合位点不同。TIP肽是TNF凝集素样结构域的合成模拟物,在肺水肿模型中可显著增加肺泡液体清除率并改善肺顺应性。在本综述中,我们将讨论TNF在肺水肿中的双重作用。

缩写

肿瘤坏死因子(TNF);急性肺损伤(ALI);急性呼吸窘迫综合征(ARDS);呼气末正压(PEEP);上皮钠通道(ENaC);神经前体细胞表达的发育下调(基因4)蛋白(Nedd4-2);血清和糖皮质激素依赖性激酶(Sgk-1);胰岛素样生长因子1(IGF-1);蛋白激酶C(PKC);活性氧(ROS);肌球蛋白轻链(MLC);肺炎溶血素(PLY);李斯特菌溶血素(LLO);白细胞介素(IL);支气管肺泡灌洗液(BALF);卡介苗(BCG);肿瘤坏死因子1型受体(TNFR1);肿瘤坏死因子2型受体(TNF-R2);

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