RhoA regulates lipopolysaccharide-induced lung cell injury via the Wnt/β-catenin pathway

被引:8
作者
Chen, Guanhua [1 ]
Sun, Xuedong [1 ]
Dong, Chunxiao [2 ]
机构
[1] Cent Hosp Shengli Oil Field Shandong, Dept Emergency, 31 Jinan Rd, Dongying 257000, Shandong, Peoples R China
[2] Cent Hosp Shengli Oil Field Shandong, Dept Pediat, Dongying 257000, Shandong, Peoples R China
关键词
acute lung injury; lipopolysaccharide; Ras homolog family member A; Wnt/beta-catenin; MICE; REGENERATION; FIBROBLASTS; ACTIVATION; EXPRESSION; RATS;
D O I
10.3892/mmr.2017.7662
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Ras homolog family member A (RhoA) has been reported to be involved in numerous biological processes; however, the effects of RhoA on acute lung injury (ALI) have yet to be reported. The present study aimed to explore how RhoA affects cell viability, reactive oxygen species (ROS) activity and cell apoptosis in a cell model of lipopolysaccharide (LPS)-induced ALI. An MTT assay, flow cytometry, reverse transcription-quantitative polymerase chain reaction and western blotting were used to determine the effects of RhoA on cell viability, apoptosis and ROS activity. The results demonstrated that RhoA inactivation was able to promote cell viability, and decrease apoptosis and ROS activity of LPS-treated cells. The results of western blotting indicated that RhoA activated the downstream Wnt/beta-catenin signaling pathway and inhibited the expression of apoptotic factors. These findings suggested that RhoA may be involved in ALI progression and could be a novel therapeutic target for this disease.
引用
收藏
页码:8501 / 8506
页数:6
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