Effect of annexin A2 on hepatopulmonary syndrome rat serum-induced proliferation of pulmonary arterial smooth muscle cells

被引:18
|
作者
Zeng, Jing [1 ,2 ]
Yi, Bin [1 ]
Wang, Zhi [1 ]
Ning, Jiaolin [1 ]
Wang, Xiaobin [2 ]
Lu, Kaizhi [1 ]
机构
[1] Third Mil Med Univ, Southwest Hosp, Dept Anesthesia, Chongqing 400038, Peoples R China
[2] Luzhou Med Coll, Dept Anesthesia, Affiliated Hosp 1, Luzhou 646000, Sichuan, Peoples R China
基金
美国国家科学基金会;
关键词
Proliferation; Pulmonary arterial smooth muscle cells; Annexin A2; Hepatopulmonary syndrome; HYPOXIA-INDUCED PROLIFERATION; NF-KAPPA-B; UP-REGULATION; HEPATOCELLULAR-CARCINOMA; NUCLEAR TRANSLOCATION; PHENOTYPE MODULATION; SIGNALING PATHWAY; LIVER-DISEASE; EXPRESSION; PHOSPHORYLATION;
D O I
10.1016/j.resp.2012.09.009
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Hepatopulmonary syndrome (HPS) is characterizes by an arterial oxygenation defect induced by intrapulmonary vasodilation that increase morbidity and mortality. However, the underlying mechanisms on HPS-associated pulmonary vascular remodeling remains undefined. In this study, we found that HPS rat serum, drawn from common bile duct ligation (CBDL) rats, mediated the overexpression of ANXA2 and the proliferation of PASMCs. And small interfering RNA (siRNA) that target rat ANXA2 led to significant downregulation of ANXA2, which resulted in the decreased proliferation of PASMCs. Subsequently, we further examined the role of ANXA2 siRNA in the regulation of pro-proliferative signaling such as that mediated by ERK1/2 and NF-kappa B, and found the attenuation of HPS-associated activation of the signaling pathway. Thus, the fact highlighted the crucial role of ANXA2 in HPS-associated PASMC proliferation, and suggested a potential therapeutic effect on HPS-associated pulmonary vascular remodeling. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:332 / 338
页数:7
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