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本文引用的文献

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Cigarette suppresses the expression of P4Halpha and vascular collagen production.香烟会抑制脯氨酰-4-羟化酶α亚基的表达以及血管胶原蛋白的生成。
Biochem Biophys Res Commun. 2004 Oct 15;323(2):592-8. doi: 10.1016/j.bbrc.2004.08.129.
2
Reduced endothelial nitric oxide synthase activity and concentration in fetal umbilical veins from maternal cigarette smokers.孕妇吸烟者胎儿脐静脉中内皮型一氧化氮合酶活性和浓度降低。
Am J Obstet Gynecol. 2004 Jul;191(1):346-51. doi: 10.1016/j.ajog.2003.12.040.
3
Zinc finger proteins and other transcription regulators as response proteins in benzo[a]pyrene exposed cells.锌指蛋白和其他转录调节因子作为苯并[a]芘暴露细胞中的应答蛋白。
Mutat Res. 2004 Jun 4;550(1-2):11-24. doi: 10.1016/j.mrfmmm.2004.01.004.
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Nicotinic acetylcholine receptor alpha7 subunit mediates migration of vascular smooth muscle cells toward nicotine.烟碱型乙酰胆碱受体α7亚基介导血管平滑肌细胞向尼古丁迁移。
J Pharmacol Sci. 2004 Mar;94(3):334-8. doi: 10.1254/jphs.94.334.
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Alteration of gene expression profiles of peripheral mononuclear blood cells by tobacco smoke: implications for periodontal diseases.
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Response of human mammary epithelial cells to DNA damage induced by BPDE: involvement of novel regulatory pathways.人乳腺上皮细胞对BPDE诱导的DNA损伤的反应:新调控途径的参与
Carcinogenesis. 2003 Feb;24(2):225-34. doi: 10.1093/carcin/24.2.225.
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Identification of pyridine compounds in cigarette smoke solution that inhibit growth of the chick chorioallantoic membrane.
Toxicol Sci. 2002 Sep;69(1):217-25. doi: 10.1093/toxsci/69.1.217.
8
Dynamic interaction of VCAM-1 and ICAM-1 with moesin and ezrin in a novel endothelial docking structure for adherent leukocytes.在一种用于黏附白细胞的新型内皮对接结构中,血管细胞黏附分子-1(VCAM-1)和细胞间黏附分子-1(ICAM-1)与膜突蛋白(moesin)和埃兹蛋白(ezrin)的动态相互作用。
J Cell Biol. 2002 Jun 24;157(7):1233-45. doi: 10.1083/jcb.200112126.
9
Heavy and light cigarette smokers have similar dysfunction of endothelial vasoregulatory activity: an in vivo and in vitro correlation.重度和轻度吸烟者具有相似的内皮血管调节活性功能障碍:体内和体外的相关性。
J Am Coll Cardiol. 2002 Jun 5;39(11):1758-63. doi: 10.1016/s0735-1097(02)01859-4.
10
Functional proteomics; current achievements.功能蛋白质组学:当前的成就
J Chromatogr B Analyt Technol Biomed Life Sci. 2002 May 5;771(1-2):89-106. doi: 10.1016/s1570-0232(02)00074-0.

香烟烟雾水溶性成分对人主动脉内皮细胞的影响——蛋白质组学方法

Effect of water-soluble fraction of cigarette smoke on human aortic endothelial cells--a proteomic approach.

作者信息

Raveendran M, Senthil D, Utama B, Shen Y, Wang J, Zhang Y, Wang X L

机构信息

Division of Cardiothoracic Surgery, Michael E. DeBakey Department of Surgery, Baylor College of Medicine, Houston, Texas 77030, USA.

出版信息

Cell Biol Toxicol. 2005 Jan;21(1):27-40. doi: 10.1007/s10565-005-1472-8.

DOI:10.1007/s10565-005-1472-8
PMID:15868486
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1283132/
Abstract

Proteomic analysis is an important investigative tool used to systematically explore cellular proteins that are responsive to adverse environmental challenges. Tobacco smoking is the second major cause of death in the world. In this study, we utilized two-dimensional electrophoresis (2-DE) and mass spectrometry (MS) technologies to explore protein changes in human aortic endothelial cells (HAECs) in response to cigarette smoke extracts (CSE). Among 389 individual proteins resolved using 2-DE, 43 had a 2- to 3-fold change in levels as measured by spot intensity and 32 had more than a 3-fold change. Sixteen of the 32 spots with sufficient amount of proteins were excised for identification by performing matrix-assisted laser desorption/ionization (MALDI)-MS analysis. Using a peptide mass fingerprinting (PMF) to search the nrNCBI database, we identified all these 16 proteins, which were either increased (n = 9) or decreased (n = 7) after CSE treatment. All these proteins have known functions, however, none have been reported to be altered after CSE treatment. The findings from our study suggest that utilizing a systemic investigative tool, such as the proteomic approach using 2-DE, may play an important role in discovering novel molecular mechanisms for cigarette smoking-induced pathological changes. Further investigation following the systemic discoveries must be further examined as they may potentially lead to new therapeutic approaches to smoking-induced diseases - a health issue affecting everyone in the world.

摘要

蛋白质组学分析是一种重要的研究工具,用于系统地探索对不利环境挑战有反应的细胞蛋白质。吸烟是世界上第二大主要死因。在本研究中,我们利用二维电泳(2-DE)和质谱(MS)技术来探索人主动脉内皮细胞(HAECs)中响应香烟烟雾提取物(CSE)的蛋白质变化。在使用2-DE分离出的389种个体蛋白质中,有43种蛋白质斑点强度测量显示水平有2至3倍的变化,32种蛋白质有超过3倍的变化。对32个有足够蛋白质量的斑点中的16个进行切除,通过基质辅助激光解吸/电离(MALDI)-MS分析进行鉴定。使用肽质量指纹图谱(PMF)搜索nrNCBI数据库,我们鉴定了所有这16种蛋白质,它们在CSE处理后要么增加(n = 9)要么减少(n = 7)。所有这些蛋白质都有已知功能,然而,尚无报道称它们在CSE处理后会发生改变。我们研究的结果表明,利用一种系统性的研究工具,如使用2-DE的蛋白质组学方法,可能在发现吸烟诱导病理变化的新分子机制方面发挥重要作用。在这些系统性发现之后的进一步研究必须进一步审查,因为它们可能潜在地导致针对吸烟诱导疾病的新治疗方法——这是一个影响世界上每个人的健康问题。