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首页> 外文期刊>Acta Neurochirurgica >Relationship between lectin-like oxidized low-density lipoprotein receptor 1 expression and preoperative echogenic findings of vulnerable carotid plaque.
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Relationship between lectin-like oxidized low-density lipoprotein receptor 1 expression and preoperative echogenic findings of vulnerable carotid plaque.

机译:凝集素样氧化的低密度脂蛋白受体1表达与易损颈动脉斑块术前回声发现之间的关系。

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摘要

PURPOSE: Lectin-like oxidized low-density lipoprotein 1 (LOX1) is an important cell surface receptor for the progression of atherosclerosis. Our purpose is to clarify the relationships of LOX1 and atherosclerotic factors for the vulnerability of carotid plaque and preoperative echogenic findings. METHODS: We examined LOX1 expression, matrix metalloproteinase (MMP)-2,9, and tissue inhibitor of MMP (TIMP)-2 by immunohistochemical analysis using carotid endarterectomy specimens obtained from 14 patients. Groups were divided into stable plaque group A and vulnerable plaque group B by preoperative echogenic findings of carotid plaques. Endothelial immunoreactivity was calculated, and the immunohistochemical findings were compared. RESULTS: LOX1 was remarkably expressed, especially in smooth muscle cells in vulnerable plaque and colocalized in MMP-9 positive cells and apoptotic cells. All LOX1, MMP-2,9, and TIMP2 were remarkably expressed in the subendothelial layer in group B compared with group A. The endothelial LOX1 index was 63.75 +/- 4.92 in group A and 83.0 +/- 5.02 in group B (p = 0.02). The endothelial MMP-2 index was 24.38 +/- 5.50 in group A and 32.83 +/- 6.79 in group B (p = 0.01). The endothelial MMP-9 index was 46.13 +/- 6.31 in group A and 59.17 +/- 2.14 in group B (p = 0.002). The endothelial TIMP-2 index had no significant difference between two groups (p = 0.14). CONCLUSION: LOX-1 may play an important role in the progression of vulnerable carotid plaque and might regulate vulnerable plaque formation in cooperation with MMPs and TIMP-2. Endothelial MMP-2 might suppress TIMP-2 activation in vulnerable plaques.
机译:目的:凝集素样氧化的低密度脂蛋白1(LOX1)是动脉粥样硬化进展的重要细胞表面受体。我们的目的是弄清LOX1和动脉粥样硬化因子与颈动脉斑块易损性和术前回声发现之间的关系。方法:我们使用14例颈动脉内膜切除术标本,通过免疫组织化学分析检查了LOX1表达,基质金属蛋白酶(MMP)-2,9和组织抑制剂MMP(TIMP)-2。根据术前颈动脉斑块的回声发现,将其分为稳定斑块A组和脆弱斑块B组。计算内皮免疫反应性,并比较免疫组化结果。结果:LOX1表达明显,特别是在易损斑块的平滑肌细胞中,并共定位于MMP-9阳性细胞和凋亡细胞中。与A组相比,B组的内皮下层中所有LOX1,MMP-2、9和TIMP2均显着表达。A组的内皮LOX1指数为63.75 +/- 4.92,B组为83.0 +/- 5.02(p = 0.02)。 A组的内皮MMP-2指数为24.38 +/- 5.50,B组为32.83 +/- 6.79(p = 0.01)。 A组的内皮MMP-9指数为46.13 +/- 6.31,B组为59.17 +/- 2.14(p = 0.002)。两组之间的内皮TIMP-2指数无显着性差异(p = 0.14)。结论:LOX-1可能在脆弱颈动脉斑块的进展中起重要作用,并可能与MMPs和TIMP-2协同调节脆弱斑块的形成。内皮MMP-2可能抑制易损斑块中TIMP-2的活化。

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