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

被引:15
作者
Fang, Xiang-Zhi [1 ]
Huang, Tian-Feng [1 ]
Wang, Cun-Jin [1 ]
Ge, Ya-Li [1 ]
Lin, Shun-Yan [1 ]
Yang-Zhang [1 ]
Gao, Ju [1 ]
机构
[1] Yangzhou Univ, Dept Anesthesiol, Sch Clin Med, Subei Peoples Hosp Jiangsu Prov, Yangzhou 225009, Jiangsu, Peoples R China
关键词
Preconditioning; IL-6/STAT3; SOCS3; Lung injury; Mechanical ventilation; RESPIRATORY-DISTRESS-SYNDROME; DEFORMATION-INDUCED INJURY; ALVEOLAR EPITHELIAL-CELLS; INFLAMMATORY RESPONSE; ENDOTHELIAL-CELLS; UP-REGULATION; INTERLEUKIN-6; PATHWAY; APOPTOSIS; BLOCKADE;
D O I
10.1016/j.intimp.2015.12.017
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
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.
引用
收藏
页码:66 / 73
页数:8
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