Suppr超能文献

丙二醛-乙醛(MAA)加合蛋白与动脉粥样硬化诱导的血管炎性损伤的关联。

Association of malondialdehyde-acetaldehyde (MAA) adducted proteins with atherosclerotic-induced vascular inflammatory injury.

作者信息

Hill G E, Miller J A, Baxter B T, Klassen L W, Duryee M J, Tuma D J, Thiele G M

机构信息

Department of Internal Medicine, University of Nebraska Medical Center, Omaha 68198-4455, USA.

出版信息

Atherosclerosis. 1998 Nov;141(1):107-16. doi: 10.1016/s0021-9150(98)00153-1.

Abstract

Atherosclerosis is a vascular injury characterized by elevated tissue levels of tumor necrosis factor-alpha (TNF-alpha), increased expression of endothelial cell adhesion molecules, and vascular wall inflammatory cell infiltration. Foam cells are associated with atherosclerotic plaque material, and low density lipoprotein (LDL) is a lipid component of foam cells. Malondialdehyde (MDA) is an oxidative product of unsaturated fatty acids and is also present in atherosclerotic lesions. MDA-modified (adducted) proteins, including MDA-modified LDL, are present in atherosclerotic human vascular tissue. Acetaldehyde (AA) is the major metabolic product of ethanol oxidation. Both MDA and AA are highly reactive aldehydes and will combine with proteins to produce an antigenically distinct protein adduct, termed the MAA adduct. This study demonstrates that proteins modified in the presence of high concentrations of MDA can produce MAA-modified proteins in vitro. In addition, MAA adducted proteins are capable of inducing rat heart endothelial cell cultures (rHEC) to produce and release TNF-alpha, and cause rHEC upregulation of endothelial adhesion molecule expression, including ICAM-1. These adhesion molecules are required for circulating inflammatory cells to adhere to endothelium which allows inflammatory cell tissue infiltration. Additionally, MAA modified proteins were defected in human atherosclerotic aortic vascular tissue but not in normal aortic tissue. Since atherosclerosis is associated with an inflammatory vascular injury characterized by elevated tissue TNF-alpha concentrations and inflammatory cell infiltration, these data suggest that MAA-adducted proteins may be formed in atherosclerotic plaque material and may be involved in the inflammatory reaction that occurs in atherosclerosis. These data further suggest that previous studies demonstrating MDA modified protein in atherosclerotic plaque may in fact have MAA modified proteins associated with them.

摘要

动脉粥样硬化是一种血管损伤,其特征在于组织中肿瘤坏死因子-α(TNF-α)水平升高、内皮细胞粘附分子表达增加以及血管壁炎性细胞浸润。泡沫细胞与动脉粥样硬化斑块物质相关,低密度脂蛋白(LDL)是泡沫细胞的一种脂质成分。丙二醛(MDA)是不饱和脂肪酸的氧化产物,也存在于动脉粥样硬化病变中。MDA修饰(加合)的蛋白质,包括MDA修饰的LDL,存在于动脉粥样硬化的人体血管组织中。乙醛(AA)是乙醇氧化的主要代谢产物。MDA和AA都是高反应性醛类,会与蛋白质结合产生一种抗原性不同的蛋白质加合物,称为MAA加合物。本研究表明,在高浓度MDA存在下修饰的蛋白质在体外可产生MAA修饰的蛋白质。此外,MAA加合的蛋白质能够诱导大鼠心脏内皮细胞培养物(rHEC)产生和释放TNF-α,并导致rHEC上调内皮粘附分子的表达,包括细胞间粘附分子-1(ICAM-1)。这些粘附分子是循环炎性细胞粘附于内皮所必需的,从而允许炎性细胞浸润组织。此外,在人类动脉粥样硬化主动脉血管组织中检测到MAA修饰的蛋白质,但在正常主动脉组织中未检测到。由于动脉粥样硬化与以组织TNF-α浓度升高和炎性细胞浸润为特征的炎性血管损伤相关,这些数据表明MAA加合的蛋白质可能在动脉粥样硬化斑块物质中形成,并可能参与动脉粥样硬化中发生的炎症反应。这些数据进一步表明,先前在动脉粥样硬化斑块中证明有MDA修饰蛋白质的研究实际上可能与之相关的是MAA修饰的蛋白质。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验