TRIM37 inhibits PDGF-BB-induced proliferation and migration of airway smooth muscle cells

被引:30
作者
Dai, Ying [1 ]
Li, Ying [1 ]
Cheng, Ruiduo [1 ]
Gao, Jie [1 ]
Li, Yanyang [1 ]
Lou, Chunyan [1 ]
机构
[1] Henan Univ, Dept Pediat, Huaihe Hosp, 115 Ximen St, Kaifeng 475000, Henan, Peoples R China
关键词
Asthma; TRIM37; Airway smooth muscle cells (ASMCs); Proliferation; Migration; GROWTH-FACTOR; CANCER CELLS; ASTHMA; EXPRESSION; CATENIN; PATHWAY; MECHANISMS; AUTOPHAGY; TARGET;
D O I
10.1016/j.biopha.2018.02.057
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Tripartite motif 37 (TRIM37) belongs to the TRIM family of proteins and has been reported to be involved in the progression of asthma. However, the effects of TRIM37 on airway smooth muscle cells (ASMCs) proliferation and migration are still unknown. This study aimed to investigate the effects of TRIM37 on cell proliferation and migration in platelet-derived growth factor BB (PDGF-BB)-stimulated ASMCs, and the potential molecular mechanisms was also explored. Our data demonstrated that the expression of TRIM37 was significantly decreased in ASMCs stimulated with PDGF-BB. In addition, overexpression of TRIM37 efficiently suppressed PDGF-BB-induced ASMCs proliferation and migration. Furthermore, overexpression of TRIM37 obviously inhibited the protein expression levels of beta-catenin, c-Myc and cyclinD1 in PDGF-BB-stimulated ASMCs. The Wnt/beta-catenin pathway activator LiCl significantly reversed the inhibitory effects of TRIM37 on cell proliferation and migration in PDGF-BB-stimulated ASMCs. Taken together, these results demonstrate that TRIM37 inhibits the proliferation and invasion of ASMCs cultured with PDGF-BB through suppressing the Wnt/beta-catenin signaling pathway.
引用
收藏
页码:24 / 29
页数:6
相关论文
共 32 条
[1]   Remodeling in asthma [J].
Al-Muhsen, Saleh ;
Johnson, Jill R. ;
Hamid, Qutayba .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2011, 128 (03) :451-462
[2]  
Bentley J Kelley, 2008, Proc Am Thorac Soc, V5, P89, DOI 10.1513/pats.200705-063VS
[3]   TRIM37 is a new histone H2A ubiquitin ligase and breast cancer oncoprotein [J].
Bhatnagar, Sanchita ;
Gazin, Claude ;
Chamberlain, Lynn ;
Ou, Jianhong ;
Zhu, Xiaochun ;
Tushir, Jogender S. ;
Virbasius, Ching-Man ;
Lin, Ling ;
Zhu, Lihua J. ;
Wajapeyee, Narendra ;
Green, Michael R. .
NATURE, 2014, 516 (7529) :116-U313
[4]   PLATELET-DERIVED GROWTH-FACTOR IN ASTHMA [J].
CHANEZ, P ;
VIGNOLA, M ;
STENGER, R ;
VIC, P ;
MICHEL, FB ;
BOUSQUET, J .
ALLERGY, 1995, 50 (11) :878-883
[5]   Wnt/β-catenin signaling in development and disease [J].
Clevers, Hans .
CELL, 2006, 127 (03) :469-480
[6]   γ-Tocotrienol reduces human airway smooth muscle cell proliferation and migration [J].
Harada, Tomoya ;
Yamasaki, Akira ;
Chikumi, Hiroki ;
Hashimoto, Kiyoshi ;
Okazaki, Ryota ;
Takata, Miki ;
Fukushima, Takehito ;
Watanabe, Masanari ;
Kurai, Jun ;
Halayko, Andrew J. ;
Shimizu, Eiji .
PULMONARY PHARMACOLOGY & THERAPEUTICS, 2015, 32 :45-52
[7]  
Hirst Stuart J, 2004, J Allergy Clin Immunol, V114, pS2, DOI 10.1016/j.jaci.2004.04.039
[8]   Platelets stimulate airway smooth muscle cell proliferation through mechanisms involving 5-lipoxygenase and reactive oxygen species [J].
Holm, Ann-Charlotte B. Svensson ;
Bengtsson, Torbjon ;
Grenegard, Magnus ;
Lindstrom, Eva G. .
PLATELETS, 2008, 19 (07) :528-536
[9]   Expression of vascular endothelial growth factor, basic fibroblast growth factor, and angiogenin immunoreactivity in asthmatic airways and its relationship to angiogenesis [J].
Hoshino, M ;
Takahashi, M ;
Aoike, N .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2001, 107 (02) :295-301
[10]   Updated Prevalences of Asthma, Allergy, and Airway Symptoms, and a Systematic Review of Trends over Time for Childhood Asthma in Shanghai, China [J].
Huang, Chen ;
Liu, Wei ;
Hu, Yu ;
Zou, Zhijun ;
Zhao, Zhuohui ;
Shen, Li ;
Weschler, Louise B. ;
Sundell, Jan .
PLOS ONE, 2015, 10 (04)