首页> 外文期刊>International immunopharmacology >Preconditioning of physiological cyclic stretch attenuated HMGB1 expression in pathologically mechanical stretch-activated A549 cells and ventilator-induced lung injury rats through inhibition of IL-6/STAT3/SOCS3
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Preconditioning of physiological cyclic stretch attenuated HMGB1 expression in pathologically mechanical stretch-activated A549 cells and ventilator-induced lung injury rats through inhibition of IL-6/STAT3/SOCS3

机译:通过抑制IL-6 / STAT3 / SOCS3预处理生理性机械拉伸激活的A549细胞和呼吸机诱发的肺损伤大鼠的生理性环状拉伸减弱的HMGB1表达

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摘要

Previous studies have shown that physiologically cyclic stretch (5% CS) attenuated both oxidative- and LPS-induced increases in HMGB1 expression via STAT3. However, little information exists about the effect of precondition of physiological cyclic stretch (CS) on the expression of HMGB 1, which play a crucial role in ventilator induced lung injury (VILI). We found that 5% CS-preconditioning significantly inhibited HMGB 1 expression, but not HMGB 1 receptors. 5% CS-preconditioning inhibits the IL-6/STAT3 pathway, and the inhibitory effect on the expression of HMGB 1 induced by 5% CS-preconditioning is abolished by additional treatment of rmlL-6. 5% CS-preconditioning also induces SOCS3 upregulation, and 5% CS-preconditioning fails to inhibit the IL-6/STAT3 pathway in cells transfected with SOCS3 siRNA. Moreover, low tidal volume ventilation preconditioning also decreases the severity of VILI evidenced by the markedly improved pulmonary alveolar-capillary barrier dysfunction, wet/dry weight ratio, and histological analysis. These results suggest that preconditioning of physiological 5% CS can reduce the expression of HMGB 1 induced by pathologically mechanical stretch through IL-6/STAT3 pathway associated with up-regulated SOCS3 expression. (C) 2015 Elsevier B.V. All rights reserved.
机译:先前的研究表明,生理循环拉伸(5%CS)通过STAT3减弱了HMGB1表达的氧化和LPS诱导的增加。但是,关于生理循环拉伸(CS)的前提条件对HMGB 1表达的影响的信息很少,HMGB 1在呼吸机诱发的肺损伤(VILI)中起着至关重要的作用。我们发现5%的CS预处理可显着抑制HMGB 1表达,但不能抑制HMGB 1受体。 5%CS预处理可抑制IL-6 / STAT3途径,而rmlL-6的额外处理可消除5%CS预处理对HMGB 1表达的抑制作用。 5%CS预处理也会诱导SOCS3上调,而5%CS预处理则无法抑制转染SOCS3 siRNA的细胞中IL-6 / STAT3途径。此外,低潮气量通气预处理还可以显着改善肺泡-毛细血管屏障功能障碍,干/湿重比和组织学分析,从而降低VILI的严重程度。这些结果表明,生理学上5%的CS的预处理可以通过与上调的SOCS3表达相关的IL-6 / STAT3途径通过病理学机械拉伸诱导的HMGB 1的表达降低。 (C)2015 Elsevier B.V.保留所有权利。

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