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Specific induction of adhesion molecules in human vascular endothelial cells by rat experimental pancreatitis-associated ascitic fluids.

机译:大鼠实验性胰腺炎相关性腹水对人血管内皮细胞黏附分子的特异性诱导。

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摘要

The molecular mechanisms that link acute pancreatitis (AP) and multiple organ failure remain unknown. To clarify the role of endothelial activation, we examined the effects of ascitic fluids from rats with experimental pancreatitis on the expression of adhesion molecules in human umbilical vein endothelial cells (HUVECs). Necrotizing hemorrhagic pancreatitis was induced with sodium taurocholate. Six and 24 h later, peritoneal exudates were collected, centrifuged and HUVECs were treated with the supernatants. The expression of E-selectin, intercellular adhesion molecule-1 (ICAM-1) and vascular cell adhesion molecule-1 (VCAM-1) was quantified by enzyme-linked immunosorbent assay. Induction of mRNA was assessed by reverse-transcriptase polymerase chain reaction. The activation of transcription factors was examined by electrophoretic mobility shift assay. The expression of ICAM-1 in the tissues was examined immunohistochemically. ICAM-1 and VCAM-1, but not E-selectin expression was upregulated with comparable mRNA induction. Nuclear factor kappaB was activated, while activator protein-1 binding activity was not altered. Immunohistochemically, enhanced ICAM-1 expression was observed in the pancreas and lung, but not in the liver. Ascitic fluids may contain soluble factors responsible for the transcriptional activation of endothelial adhesion molecules, and ICAM-1 may play roles in the pathogenesis of complicated AP.
机译:链接急性胰腺炎(AP)和多器官衰竭的分子机制仍然未知。为了阐明内皮细胞激活的作用,我们检查了实验性胰腺炎大鼠腹水对人脐静脉内皮细胞(HUVEC)黏附分子表达的影响。牛磺胆酸钠诱发坏死性出血性胰腺炎。 6和24小时后,收集腹膜渗出液,离心并用上清液处理HUVEC。通过酶联免疫吸附法定量分析E-选择蛋白,细胞间粘附分子-1(ICAM-1)和血管细胞粘附分子-1(VCAM-1)的表达。通过逆转录酶聚合酶链反应评估mRNA的诱导。通过电泳迁移率变动分析检查转录因子的激活。免疫组织化学检查ICAM-1在组织中的表达。 ICAM-1和VCAM-1,但不是E-选择素表达被可比的mRNA诱导上调。核因子κB被激活,而激活蛋白-1的结合活性没有改变。免疫组织化学观察到,在胰腺和肺中观察到了增强的ICAM-1表达,但在肝脏中未观察到。腹水可能含有负责内皮粘附分子转录激活的可溶性因子,ICAM-1可能在复杂AP的发病机制中发挥作用。

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