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本文引用的文献

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Subcellular localization of tyrosine-nitrated proteins is dictated by reactive oxygen species generating enzymes and by proximity to nitric oxide synthase.酪氨酸硝化蛋白的亚细胞定位由产生活性氧的酶以及与一氧化氮合酶的接近程度决定。
Free Radic Biol Med. 2006 Jun 1;40(11):1903-13. doi: 10.1016/j.freeradbiomed.2005.09.006. Epub 2005 Nov 15.
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Oxidized phospholipids, Lp(a) lipoprotein, and coronary artery disease.氧化磷脂、脂蛋白(a)与冠状动脉疾病
N Engl J Med. 2005 Jul 7;353(1):46-57. doi: 10.1056/NEJMoa043175.
3
Activated antigen-presenting cells select and present chemically modified peptides recognized by unique CD4 T cells.活化的抗原呈递细胞选择并呈递由独特的CD4 T细胞识别的化学修饰肽段。
Proc Natl Acad Sci U S A. 2005 May 31;102(22):7928-33. doi: 10.1073/pnas.0502255102. Epub 2005 May 18.
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Apolipoprotein A-I is a selective target for myeloperoxidase-catalyzed oxidation and functional impairment in subjects with cardiovascular disease.载脂蛋白A-I是心血管疾病患者中髓过氧化物酶催化氧化和功能损伤的选择性靶点。
J Clin Invest. 2004 Aug;114(4):529-41. doi: 10.1172/JCI21109.
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Proinflammatory activity of anti-IL-8 autoantibody:IL-8 complexes in alveolar edema fluid from patients with acute lung injury.抗白细胞介素-8自身抗体:急性肺损伤患者肺泡水肿液中白细胞介素-8复合物的促炎活性
Am J Physiol Lung Cell Mol Physiol. 2004 Jun;286(6):L1105-13. doi: 10.1152/ajplung.00277.2003. Epub 2004 Jan 16.
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Cutting edge: MHC class II-restricted peptides containing the inflammation-associated marker 3-nitrotyrosine evade central tolerance and elicit a robust cell-mediated immune response.
J Immunol. 2003 Jul 15;171(2):528-32. doi: 10.4049/jimmunol.171.2.528.
8
Protein tyrosine nitration in the mitochondria from diabetic mouse heart. Implications to dysfunctional mitochondria in diabetes.糖尿病小鼠心脏线粒体中的蛋白质酪氨酸硝化。对糖尿病中线粒体功能障碍的影响。
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Expression of inducible nitric-oxide synthase and intracellular protein tyrosine nitration in vascular smooth muscle cells: role of reactive oxygen species.诱导型一氧化氮合酶在血管平滑肌细胞中的表达及细胞内蛋白酪氨酸硝化:活性氧的作用
J Biol Chem. 2003 Jun 20;278(25):22901-7. doi: 10.1074/jbc.M210806200. Epub 2003 Apr 10.
10
Future research directions in acute lung injury: summary of a National Heart, Lung, and Blood Institute working group.急性肺损伤的未来研究方向:美国国立心肺血液研究所工作组总结
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重大创伤后急性肺损伤患者中识别识别3-硝基酪氨酸的免疫球蛋白。

Identification of immunoglobulins that recognize 3-nitrotyrosine in patients with acute lung injury after major trauma.

作者信息

Thomson Leonor, Christie Jason, Vadseth Caryn, Lanken Paul N, Fu Xiaoming, Hazen Stanley L, Ischiropoulos Harry

机构信息

Stokes Research Institute, Children's Hospital of Philadelphia, University of Pennsylvania School of Medicine, PA 19104-4318, USA.

出版信息

Am J Respir Cell Mol Biol. 2007 Feb;36(2):152-7. doi: 10.1165/rcmb.2006-0288SM. Epub 2006 Oct 5.

DOI:10.1165/rcmb.2006-0288SM
PMID:17023686
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1899311/
Abstract

Tyrosine nitration is a nitric oxide-derived post-translational modification of proteins. Elevated levels of specific plasma proteins modified by tyrosine nitration have been detected during acute and chronic inflammatory conditions, including acute lung injury (ALI). In the present study we examined whether circulating immunoglobulins against nitrated proteins are present in the plasma of subjects with clinically documented ALI. Affinity chromatography using covalently linked 3-nitrotyrosine was employed to identify plasma proteins that bind to this unusual amino acid. Western blotting and liquid chromatography-tandem mass spectrometry of in-gel digested protein bands revealed that the major proteins eluted from the affinity column were IgM and IgG. An enzyme-linked immunosorbent assay (ELISA) based on competition of horseradish peroxidase-derivatized 3-nitrotyrosine binding to plasma with unlabeled 3-nitrotyrosine was developed and validated. Using this ELISA, the levels of immunoglobulins that recognize 3-nitrotyrosine were significantly higher in the plasma of subjects with ALI compared with both normal control subjects and subjects with major trauma who did not develop ALI (0.36+/- 0.14 versus 0.03 +/- 0.05, and 0.25 +/- 0.15; P < 0.001 and P = 0.006, respectively). These data indicate that tyrosine-nitrated proteins induce the production of specific immunoglobulins during acute phase response and inflammation.

摘要

酪氨酸硝化是一种由一氧化氮介导的蛋白质翻译后修饰。在急性和慢性炎症状态下,包括急性肺损伤(ALI),已检测到经酪氨酸硝化修饰的特定血浆蛋白水平升高。在本研究中,我们检测了临床诊断为ALI的受试者血浆中是否存在针对硝化蛋白的循环免疫球蛋白。使用共价连接3 - 硝基酪氨酸的亲和色谱法来鉴定与这种特殊氨基酸结合的血浆蛋白。对凝胶内消化的蛋白条带进行蛋白质印迹和液相色谱 - 串联质谱分析显示,从亲和柱洗脱的主要蛋白质是IgM和IgG。基于辣根过氧化物酶衍生的3 - 硝基酪氨酸与未标记的3 - 硝基酪氨酸竞争结合血浆的酶联免疫吸附测定(ELISA)被开发并验证。使用该ELISA,与正常对照受试者和未发生ALI的严重创伤受试者相比,ALI受试者血浆中识别3 - 硝基酪氨酸的免疫球蛋白水平显著更高(分别为0.36±0.14与0.03±0.05和0.25±0.15;P < 0.001和P = 0.006)。这些数据表明,酪氨酸硝化蛋白在急性期反应和炎症过程中诱导特定免疫球蛋白的产生。