Henriksen Peter A, Sallenave Jean-Michel
Department of Cardiology, The Royal Infirmary of Edinburgh, Old Dalkeith Road, Edinburgh EH16 4SA, UK.
Int J Biochem Cell Biol. 2008;40(6-7):1095-100. doi: 10.1016/j.biocel.2008.01.004. Epub 2008 Jan 11.
Human neutrophil elastase (HNE) is present within atherosclerotic plaques where it contributes to matrix degradation and weakening of the vessel wall associated with the complications of aneurysm formation and plaque rupture. It is joined by other extracellular proteases in these actions but the broad range of substrates and potency of HNE coupled with the potential for rapid increases in HNE activity associated with neutrophil degranulation in acute coronary syndromes single this disruptive protease out as therapeutic target in atherosclerotic disease. This review summarises the role of HNE in neutrophil-mediated endothelial injury and the evidence for HNE as a mediator of atherosclerotic plaque development. The therapeutic potential of HNE neutralising antiproteases, alpha-1-antitrypsin and elafin, in atherosclerosis, is discussed.
人类中性粒细胞弹性蛋白酶(HNE)存在于动脉粥样硬化斑块中,它会导致基质降解以及血管壁弱化,这与动脉瘤形成和斑块破裂的并发症相关。在这些作用中,它与其他细胞外蛋白酶共同发挥作用,但HNE广泛的底物范围和效力,再加上急性冠状动脉综合征中与中性粒细胞脱颗粒相关的HNE活性可能迅速增加,使得这种具有破坏性的蛋白酶成为动脉粥样硬化疾病的治疗靶点。本综述总结了HNE在中性粒细胞介导的内皮损伤中的作用,以及HNE作为动脉粥样硬化斑块发展介质的证据。还讨论了HNE中和性抗蛋白酶α-1抗胰蛋白酶和弹性蛋白在动脉粥样硬化中的治疗潜力。