Spanbroek Rainer, Grabner Rolf, Lotzer Katharina, Hildner Markus, Urbach Anja, Ruhling Katharina, Moos Michael P W, Kaiser Brigitte, Cohnert Tina U, Wahlers Thorsten, Zieske Arthur, Plenz Gabriele, Robenek Horst, Salbach Peter, Kuhn Hartmut, Radmark Olof, Samuelsson Bengt, Habenicht Andreas J R
Institute for Vascular Medicine, Friedrich-Schiller-University of Jena, Nordhäuserstrasse 78, 99089 Erfurt, Germany.
Proc Natl Acad Sci U S A. 2003 Feb 4;100(3):1238-43. doi: 10.1073/pnas.242716099. Epub 2003 Jan 27.
Oxidation products of low-density lipoproteins have been suggested to promote inflammation during atherogenesis, and reticulocyte-type 15-lipoxygenase has been implicated to mediate this oxidation. In addition, the 5-lipoxygenase cascade leads to formation of leukotrienes, which exhibit strong proinflammatory activities in cardiovascular tissues. Here, we studied both lipoxygenase pathways in human atherosclerosis. The 5-lipoxygenase pathway was abundantly expressed in arterial walls of patients afflicted with various lesion stages of atherosclerosis of the aorta and of coronary and carotid arteries. 5-lipoxygenase localized to macrophages, dendritic cells, foam cells, mast cells, and neutrophilic granulocytes, and the number of 5-lipoxygenase expressing cells markedly increased in advanced lesions. By contrast, reticulocyte-type 15-lipoxygenase was expressed at levels that were several orders of magnitude lower than 5-lipoxygenase in both normal and diseased arteries, and its expression could not be related to lesion pathology. Our data support a model of atherogenesis in which 5-lipoxygenase cascade-dependent inflammatory circuits consisting of several leukocyte lineages and arterial wall cells evolve within the blood vessel wall during critical stages of lesion development. They raise the possibility that antileukotriene drugs may be an effective treatment regimen in late-stage disease.
低密度脂蛋白的氧化产物被认为在动脉粥样硬化形成过程中促进炎症反应,而网织红细胞型15-脂氧合酶被认为介导了这种氧化反应。此外,5-脂氧合酶级联反应导致白三烯的形成,白三烯在心血管组织中表现出强烈的促炎活性。在此,我们研究了人类动脉粥样硬化中的两种脂氧合酶途径。5-脂氧合酶途径在患有主动脉、冠状动脉和颈动脉不同病变阶段动脉粥样硬化的患者动脉壁中大量表达。5-脂氧合酶定位于巨噬细胞、树突状细胞、泡沫细胞、肥大细胞和嗜中性粒细胞,在晚期病变中表达5-脂氧合酶的细胞数量显著增加。相比之下,在正常和患病动脉中,网织红细胞型15-脂氧合酶的表达水平比5-脂氧合酶低几个数量级,其表达与病变病理无关。我们的数据支持一种动脉粥样硬化形成模型,即在病变发展的关键阶段,由几种白细胞谱系和动脉壁细胞组成的依赖于5-脂氧合酶级联反应的炎症回路在血管壁内演变。这些数据增加了白三烯拮抗剂可能是晚期疾病有效治疗方案的可能性。