miR-214 is Stretch-Sensitive in Aortic Valve and Inhibits Aortic Valve Calcification

被引:0
作者
Md Tausif Salim
Joan Fernández Esmerats
Sivakkumar Arjunon
Nicolas Villa-Roel
Robert M. Nerem
Hanjoong Jo
Ajit P. Yoganathan
机构
[1] Georgia Institute of Technology,School of Chemical and Biomolecular Engineering
[2] Georgia Institute of Technology and Emory University,Wallace H. Coulter Department of Biomedical Engineering
[3] Georgia Institute of Technology,Parker H. Petit Institute for Bioengineering and Bioscience
来源
Annals of Biomedical Engineering | 2019年 / 47卷
关键词
Cyclic stretch; miR-214; Aortic valve; Calcification;
D O I
暂无
中图分类号
学科分类号
摘要
miR-214 has been recently found to be significantly downregulated in calcified human aortic valves (AVs). ER stress, especially the ATF4-mediated pathway, has also been shown to be significantly upregulated in calcific AV disease. Since elevated cyclic stretch is one of the major mechanical stimuli for AV calcification and ATF4 is a validated target of miR-214, we investigated the effect of cyclic stretch on miR-214 expression as well as those of ATF4 and two downstream genes (CHOP and BCL2L1). Porcine aortic valve (PAV) leaflets were cyclically stretched at 15% for 48 h in regular medium and for 1 week in osteogenic medium to simulate the early remodeling and late calcification stages of stretch-induced AV disease, respectively. For both stages, 10% cyclic stretch served as the physiological counterpart. RT-qPCR revealed that miR-214 expression was significantly downregulated during the late calcification stage, whereas the mRNA expression of ATF4 and BCL2L1 was upregulated and downregulated, respectively, during both early remodeling and late calcification stages. When PAV leaflets were statically transfected with miR-214 mimic in osteogenic medium for 2 weeks, calcification was significantly reduced compared to the control mimic case. This implies that miR-214 may have a protective role in stretch-induced calcific AV disease.
引用
收藏
页码:1106 / 1115
页数:9
相关论文
共 460 条
[1]  
Arjunon S(2013)Aortic valve: mechanical environment and mechanobiology Ann. Biomed. Eng. 41 1331-1346
[2]  
Rathan S(2016)The transcription factor scleraxis is a critical regulator of cardiac fibroblast phenotype BMC Biol. 14 21-H764
[3]  
Jo H(2009)Elevated cyclic stretch alters matrix remodeling in aortic valve cusps: implications for degenerative aortic valve disease Am. J. Physiol. Heart Circ. Physiol. 296 H756-57
[4]  
Yoganathan AP(2010)Elevated cyclic stretch induces aortic valve calcification in a bone morphogenic protein-dependent manner Am. J. Pathol. 177 49-435
[5]  
Bagchi RA(2011)Hemodynamics and mechanobiology of aortic valve inflammation and calcification Int. J. Inflam. 2011 263870-498
[6]  
Roche P(2004)Twist code determines the onset of osteoblast differentiation Dev. Cell 6 423-2354
[7]  
Aroutiounova N(2009)Refining molecular pathways leading to calcific aortic valve stenosis by studying gene expression profile of normal and calcified stenotic human aortic valves Circ. Genom. Precis. Med. 2 489-2392
[8]  
Espira L(2013)Endoplasmic reticulum stress participates in aortic valve calcification in hypercholesterolemic animals Arterioscler. Thromb. Vasc. Biol. 33 2345-1524
[9]  
Abrenica B(2017)Subclinical leaflet thrombosis in surgical and transcatheter bioprosthetic aortic valves: an observational study Lancet 389 2383-609
[10]  
Schweitzer R(2011)Cell-matrix interactions in the pathobiology of calcific aortic valve disease: critical roles for matricellular, matricrine, and matrix mechanics cues Circ. Res. 108 1510-559