Secreted S100A4 causes asthmatic airway epithelial barrier dysfunction induced by house dust mite extracts via activating VEGFA/VEGFR2 pathway

被引:2
|
作者
Huang, Chaowen [1 ]
Zheng, Dongyan [2 ]
Fu, Chunlai [3 ]
Cai, Ziwei [2 ]
Zhang, He [2 ]
Xie, Zhefan [3 ]
Luo, Lishan [4 ]
Li, Huifang [2 ]
Huang, Yanming [1 ,5 ]
Chen, Jialong [2 ,6 ]
机构
[1] Jiangmen Cent Hosp, Jiangmen Inst Resp Dis, Dept Pulm & Crit Care Med, Jiangmen, Peoples R China
[2] Guangdong Med Univ, Sch Publ Hlth, Dept Environm & Occupat Hlth, Dongguan, Peoples R China
[3] Southern Med Univ, Affiliated Dongguan Peoples Hosp, Dept Emergency Intens Care Unit, Dongguan, Peoples R China
[4] Huizhou Municipal Cent Hosp, Dept Resp & Crit Care Med, Huizhou, Peoples R China
[5] Sun Yat sen Univ, Jiangmen Hosp, Jiangmen Inst Resp Dis, Dept Pulm & Crit Care Med, Jiangmen, Guangdong, Peoples R China
[6] Guangdong Med Univ, Sch Publ Hlth, Dept Environm & Occupat Hlth, Dongguan, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
asthma; epithelial barrier; house dust mite; VEGFA; VEGFR2; pathway; BREAST-CANCER; RHEUMATOID-ARTHRITIS; CELL INVASION; UP-REGULATION; BETA-CATENIN; METASTASIS; PROTEIN; TRANSITION; PROMOTES;
D O I
10.1002/tox.23776
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The airway epithelial barrier dysfunction plays a crucial role in pathogenesis of asthma and causes the amplification of downstream inflammatory signal pathway. S100 calcium binding protein A4 (S100A4), which promotes metastasis, have recently been discovered as an effective inflammatory factor and elevated in bronchoalveolar lavage fluid in asthmatic mice. Vascular endothelial growth factor-A (VEGFA), is considered as vital regulator in vascular physiological activities. Here, we explored the probably function of S100A4 and VEGFA in asthma model dealt with house dust mite (HDM) extracts. Our results showed that secreted S100A4 caused epithelial barrier dysfunction, airway inflammation and the release of T-helper 2 cytokines through the activation of VEGFA/VEGFR2 signaling pathway, which could be partial reversed by S100A4 polyclonal antibody, niclosamide and S100A4 knockdown, representing a potential therapeutic target for airway epithelial barrier dysfunction in asthma.
引用
收藏
页码:1431 / 1444
页数:14
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