首页> 外文期刊>Biological & pharmaceutical bulletin >Distribution Profiles of Membrane Type-1 Matrix Metalloproteinase(MT1-MMP),Matrix Metalloproteinase-2(MMP-2)and Cyclooxygenase-2(COX-2)in Rabbit Atherosclerosis:Comparison with Plaque Instability Analysis
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Distribution Profiles of Membrane Type-1 Matrix Metalloproteinase(MT1-MMP),Matrix Metalloproteinase-2(MMP-2)and Cyclooxygenase-2(COX-2)in Rabbit Atherosclerosis:Comparison with Plaque Instability Analysis

机译:膜1型基质金属蛋白酶(MT1-MMP),基质金属蛋白酶-2(MMP-2)和环氧合酶-2(COX-2)在兔动脉粥样硬化中的分布特征:与斑块不稳定性分析的比较

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Background:Despite increasing evidence that membrane type 1 matrix metalloproteinase(MT1-MMP),matrix metalloproteinase-2(MMP-2),and cyclooxygenase-2(COX-2)are involved in the pathogenesis of atherosclerosis,the possible links among these enzymes remain unclear.Accordingly,we investigated the distribution of MT1-MMP,MMP-2,and COX-2 immunohistologically in the atherosclerotic lesions of hypercholesterolemic(WHHLMI)rabbits.Methods and Results:Distribution of MT1-MMP,MMP-2,and COX-2 was examined by immunohistochemical staining using sixty cross sections of the ascending-arch and thoracic aortas prepared from 4 WHHLMI rabbits.MT1-MMP and MMP-2 staining was prominently observed in the macrophage-rich regions of the atheromatous lesions,and was positively correlated with morphological vulnerability(r=0.63 for MT1-MMP;r=0.60 for MMP-2;p<0.0001).MT1-MMP staining was positively correlated with MMP-2 staining(r=0.61,p<0.0001).COX-2 staining was also the highest in the macrophage-rich regions of the atheromatous lesions,with relatively high staining levels in other more stable lesions.Conclusions:Co-distribution of MT1-MMP,MMP-2,and COX-2 was demonstrated in grade IV atheroma,indicating a possible link among these enzymes in the destabilization of atherosclerotic plaques.The relatively high COX-2 distribution in other more stable lesions may indicate its additional roles in the stabilization of atherosclerotic lesions.The present findings in hypercholesterolemic rabbits should help advance our understanding of the pathophysiology of atherosclerosis and provide useful information for the development of new therapeutic and diagnostic(imaging)agents that target MMPs and COX-2 in atherosclerosis.
机译:背景:尽管越来越多的证据表明膜1型基质金属蛋白酶(MT1-MMP),基质金属蛋白酶-2(MMP-2)和环氧合酶-2(COX-2)参与动脉粥样硬化的发病机制,这些酶之间可能存在联系因此,我们通过免疫组织学方法研究了高胆固醇血症(WHHLMI)兔动脉粥样硬化病变中MT1-MMP,MMP-2和COX-2的分布。方法与结果:MT1-MMP,MMP-2和COX的分布-2用4只WHHLMI兔制备的升弓和胸主动脉的60个横截面进行免疫组织化学染色检查。在动脉粥样硬化病变的巨噬细胞富集区域中MT1-MMP和MMP-2染色显着,并呈阳性与形态脆弱性相关(MT1-MMP r = 0.63; MMP-2 r = 0.60; p <0.0001).MT1-MMP染色与MMP-2染色呈正相关(r = 0.61,p <0.0001)。在t的巨噬细胞富集区域中2染色也是最高的结论:在IV级动脉粥样硬化中MT1-MMP,MMP-2和COX-2共分布,表明这些酶可能与失稳有关在其他较稳定的病变中相对较高的COX-2分布可能表明其在稳定动脉粥样硬化病变中具有额外的作用。目前在高胆固醇血症兔中的发现应有助于增进我们对动脉粥样硬化的病理生理学的了解,并为动脉粥样硬化斑块的形成提供有用的信息。针对动脉粥样硬化中MMPs和COX-2的新型治疗和诊断(影像)剂的开发。

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