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首页> 外文期刊>Thrombosis Research: An International Journal on Vascular Obstruction, Hemorrhage and Hemostasis >Down-regulation of murine tissue factor pathway inhibitor mRNA by endotoxin and tumor necrosis factor-alpha in vitro and in vivo.
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Down-regulation of murine tissue factor pathway inhibitor mRNA by endotoxin and tumor necrosis factor-alpha in vitro and in vivo.

机译:体内和体外毒素和肿瘤坏死因子-α对鼠组织因子途径抑制剂mRNA的下调。

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摘要

Tissue factor pathway inhibitor (TFPI) is the protease inhibitor that regulates the extrinsic coagulation pathway initiated by the factor VIIa/TF complex. In this study, we first investigated tissue distribution of TFPI mRNA in the mouse and found that TFPI mRNA expression level was by far the highest in the lung, followed by the heart, adrenal, and adipose tissue. Since little has been known concerning the regulation of TFPI gene expression in vivo, we further analyzed the changes in the TFPI mRNA level in murine tissues after intraperitoneal injection of lipopolysaccharide (LPS), tumor necrosis factor-alpha (TNF-alpha), and interleukin-1 (IL-1). LPS and TNF-alpha dramatically decreased TFPI mRNA expression in four tissues examined (e.g., lung, heart, kidney, and adipose tissue), whereas the suppressive effect of IL-1 on TFPI mRNA was limited. The down-regulation of TFPI mRNA expression by LPS and TNF-alpha was also observed in cultured mouse endothelial cells and in cardiomyocyte cell lines. The decreased TFPI mRNA expression by LPS and TNF-alpha in tissues and in the specific cell types may contribute to an increase in the local procoagulant potential, resulting in the thrombotic tendency under septic and/or inflammatory conditions.
机译:组织因子途径抑制剂(TFPI)是一种蛋白酶抑制剂,可调节由VIIa / TF因子复合物引发的外在凝血途径。在这项研究中,我们首先调查了TFPI mRNA在小鼠中的组织分布,发现TFPI mRNA的表达水平迄今为止在肺中最高,其次是心脏,肾上腺和脂肪组织。由于对体内TFPI基因表达的调控知之甚少,因此我们进一步分析了腹膜内注射脂多糖(LPS),肿瘤坏死因子-α(TNF-alpha)和白介素后小鼠组织中TFPI mRNA水平的变化。 -1(IL-1)。 LPS和TNF-α显着降低了所检查的四个组织(例如,肺,心脏,肾脏和脂肪组织)中TFPI mRNA的表达,而IL-1对TFPI mRNA的抑制作用是有限的。在培养的小鼠内皮细胞和心肌细胞系中也观察到LPS和TNF-α对TFPI mRNA表达的下调。 LPS和TNF-α在组织和特定细胞类型中降低的TFPI mRNA表达可能会导致局部促凝潜力的增加,从而导致在脓毒症和/或炎症条件下形成血栓形成趋势。

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