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抗磷脂抗体的血栓形成作用是由细胞间黏附分子-1、血管细胞黏附分子-1和P-选择素介导的。

Thrombogenic effects of antiphospholipid antibodies are mediated by intercellular cell adhesion molecule-1, vascular cell adhesion molecule-1, and P-selectin.

作者信息

Pierangeli S S, Espinola R G, Liu X, Harris E N

机构信息

Department of Microbiology and Immunology, Morehouse School of Medicine. Atlanta, GA 30310-1495, USA.

出版信息

Circ Res. 2001 Feb 2;88(2):245-50. doi: 10.1161/01.res.88.2.245.

Abstract

Recent studies have shown that antiphospholipid (aPL) enhances expression of intercellular cell adhesion molecule-1 (ICAM-1), vascular cell adhesion molecule-1 (VCAM-1), and E-selectin on endothelial cells (ECs) and that these effects are correlated with increased adhesion of leukocytes to endothelium in cremaster muscle in vivo and with thrombosis in a mouse model. Activation of ECs by aPL may create a hypercoagulable state that precedes and contributes to thrombosis in patients with aPL syndrome (APS). This study proposed to examine whether this in vivo activation of ECs and enhanced thrombosis by aPL are mediated by ICAM-1, P-selectin, or VCAM-1. The dynamics of thrombus formation and the number of adhering leukocytes were studied in ICAM-1-deficient (ICAM-1(-/-)) mice or ICAM-1-/P-selectin-deficient (ICAM-1(-/-)/P-selectin(-/-)) mice treated with affinity-purified aPL antibodies (ap IgG-APS) or with control IgG and compared with wild-type mice treated in a similar fashion. In another set of experiments, the adhesion of leukocytes to cremaster muscle and the dynamics of thrombus formation were studied in CD1 mice treated with aPL or control IgG before and 30 minutes after intravenous infusion with 100 microg monoclonal antibody anti-VCAM-1. The results indicate that the enhanced adhesion of leukocytes to endothelium in wild-type mice was significantly reduced in ICAM-1(-/-) and completely abrogated in ICAM-1(-/-)/P-selectin(-/-) mice treated with ap IgG-APS compared with wild-type mice treated with ap IgG-APS (6.9+/-2.3, 0.4+/-0.4 versus 35+/-12, respectively). More importantly, this correlated with a significant reduction in thrombus size compared with wild-type mice treated with ap IgG-APS (895+/-259 microm(2), 859+/-243 microm(2) versus 3816+/-672 microm(2), respectively). Infusion of the mice with anti-VCAM-1 antibodies significantly reversed the enhanced adhesion of leukocytes (14.9+/-3 to 11.3+/-2.1) and thrombus size 3830+/-1008 microm(2) versus 876+/-548 microm(2)) in mice treated with ap IgG-APS. The data indicate that ICAM-1, P-selectin, and VCAM-1 expression are important in thrombotic complications by aPL antibodies and may provide novel targets for therapy in patients with APS.

摘要

最近的研究表明,抗磷脂(aPL)可增强内皮细胞(ECs)上细胞间黏附分子-1(ICAM-1)、血管细胞黏附分子-1(VCAM-1)和E-选择素的表达,且这些效应与体内提睾肌中白细胞与内皮的黏附增加以及小鼠模型中的血栓形成相关。aPL对ECs的激活可能会导致高凝状态,这在抗磷脂综合征(APS)患者血栓形成之前出现并促使其发生。本研究旨在探讨aPL在体内对ECs的激活以及增强血栓形成是否由ICAM-1、P-选择素或VCAM-1介导。在给予亲和纯化的aPL抗体(ap IgG-APS)或对照IgG处理的ICAM-1缺陷(ICAM-1(-/-))小鼠或ICAM-1/P-选择素缺陷(ICAM-1(-/-)/P-选择素(-/-))小鼠中,研究血栓形成的动态过程以及黏附白细胞的数量,并与以类似方式处理的野生型小鼠进行比较。在另一组实验中,在静脉注射100μg抗VCAM-1单克隆抗体之前和之后30分钟,研究给予aPL或对照IgG处理的CD1小鼠中白细胞与提睾肌的黏附以及血栓形成的动态过程。结果表明,与给予ap IgG-APS处理的野生型小鼠相比,给予ap IgG-APS处理的ICAM-1(-/-)小鼠中白细胞与内皮的增强黏附显著降低,而在ICAM-1(-/-)/P-选择素(-/-)小鼠中则完全消除(分别为6.9±2.3、0.4±0.4对35±12)。更重要的是,与给予ap IgG-APS处理的野生型小鼠相比,这与血栓大小的显著减小相关(分别为895±259μm²、859±243μm²对3816±672μm²)。给小鼠注射抗VCAM-1抗体可显著逆转给予ap IgG-APS处理的小鼠中白细胞黏附增强(从14.9±3降至11.3±2.1)以及血栓大小(从3830±1008μm²降至876±548μm²)。数据表明,ICAM-1、P-选择素和VCAM-1的表达在aPL抗体引起的血栓并发症中起重要作用,可能为APS患者提供新的治疗靶点。

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