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本文引用的文献

1
ProteinQuant Suite: a bundle of automated software tools for label-free quantitative proteomics.蛋白质定量套件:一套用于无标记定量蛋白质组学的自动化软件工具。
Rapid Commun Mass Spectrom. 2008 Dec;22(23):3823-34. doi: 10.1002/rcm.3781.
2
Nitric oxide and peroxynitrite in health and disease.一氧化氮与过氧亚硝酸盐在健康与疾病中的作用
Physiol Rev. 2007 Jan;87(1):315-424. doi: 10.1152/physrev.00029.2006.
3
Proteomic modification by nitric oxide.一氧化氮对蛋白质组的修饰
J Pharmacol Sci. 2006 Aug;101(4):271-9. doi: 10.1254/jphs.crj06009x. Epub 2006 Aug 5.
4
Changes in liver protein abundance in inbred alcohol-preferring rats due to chronic alcohol exposure, as measured through a proteomics approach.通过蛋白质组学方法测定,近交系嗜酒大鼠因长期酒精暴露导致肝脏蛋白质丰度的变化。
Proteomics. 2006 May;6(10):3060-74. doi: 10.1002/pmic.200500725.
5
Protein nitration in biological aging: proteomic and tandem mass spectrometric characterization of nitrated sites.生物衰老过程中的蛋白质硝化:硝化位点的蛋白质组学和串联质谱表征
Methods Enzymol. 2005;396:160-71. doi: 10.1016/S0076-6879(05)96016-3.
6
Vascular respiratory uncoupling increases blood pressure and atherosclerosis.血管呼吸解偶联会升高血压并引发动脉粥样硬化。
Nature. 2005 May 26;435(7041):502-6. doi: 10.1038/nature03527.
7
A cluster of metabolic defects caused by mutation in a mitochondrial tRNA.由线粒体tRNA突变引起的一组代谢缺陷。
Science. 2004 Nov 12;306(5699):1190-4. doi: 10.1126/science.1102521. Epub 2004 Oct 21.
8
Mitochondrial disorders.线粒体疾病
Brain. 2004 Oct;127(Pt 10):2153-72. doi: 10.1093/brain/awh259. Epub 2004 Sep 9.
9
Mitochondrial genome mutations in hypertensive individuals.高血压个体中的线粒体基因组突变。
Am J Hypertens. 2004 Jul;17(7):629-35. doi: 10.1016/j.amjhyper.2004.02.020.
10
Premature ageing in mice expressing defective mitochondrial DNA polymerase.表达缺陷型线粒体DNA聚合酶的小鼠早衰
Nature. 2004 May 27;429(6990):417-23. doi: 10.1038/nature02517.

线粒体疾病中蛋白质硝化的增加:血管壁受累的证据。

Increased protein nitration in mitochondrial diseases: evidence for vessel wall involvement.

机构信息

Department of Neurological Sciences and Vision, Section of Clinical Neurology, University of Verona, Italy.

出版信息

Mol Cell Proteomics. 2011 Apr;10(4):M110.002964. doi: 10.1074/mcp.M110.002964. Epub 2010 Dec 14.

DOI:10.1074/mcp.M110.002964
PMID:21156839
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3069340/
Abstract

Mitochondrial diseases (MD) are heterogeneous disorders because of impairment of respiratory chain function leading to oxidative stress. We hypothesized that in MD the vascular endothelium may be affected by increased oxidative/nitrative stress causing a reduction of nitric oxide availability. We therefore, investigated the pathobiology of vasculature in MD patients by assaying the presence of 3-nitrotyrosine in muscle biopsies followed by the proteomic identification of proteins which undergo tyrosine nitration. We then measured the flow-mediated vasodilatation as a proof of altered nitric oxide generation/bioactivity. Here, we show that 3-nitrotyrosine staining is specifically located in the small vessels of muscle tissue and that the reaction is stronger and more evident in a significant percentage of vessels from MD patients as compared with controls. Eleven specific proteins which are nitrated under pathological conditions were identified; most of them are involved in energy metabolism and are located mainly in mitochondria. In MD patients the flow-mediated vasodilatation was reduced whereas baseline arterial diameters, blood flow velocity and endothelium-independent vasodilatation were similar to controls. The present results provide evidence that in MD the vessel wall is a target of increased oxidative/nitrative stress.

摘要

线粒体疾病(MD)是一种异质性疾病,因为呼吸链功能的损伤会导致氧化应激。我们假设在 MD 中,血管内皮可能会受到增加的氧化/硝化应激的影响,导致一氧化氮的可用性降低。因此,我们通过检测肌肉活检中 3-硝基酪氨酸的存在,以及对经历酪氨酸硝化的蛋白质进行蛋白质组学鉴定,来研究 MD 患者的血管病理学。然后,我们测量了血流介导的血管舒张,以证明一氧化氮生成/生物活性的改变。在这里,我们表明 3-硝基酪氨酸染色特异性地位于肌肉组织的小血管中,并且在与对照组相比,来自 MD 患者的血管中,该反应更强且更明显。在病理条件下,鉴定出了 11 种特异性硝化的蛋白质;其中大多数参与能量代谢,主要位于线粒体中。在 MD 患者中,血流介导的血管舒张减少,而基础动脉直径、血流速度和非内皮依赖性血管舒张与对照组相似。本研究结果提供了证据表明,在 MD 中,血管壁是增加的氧化/硝化应激的靶标。