Codependence of Bone Morphogenetic Protein Receptor 2 and Transforming Growth Factor-β in Elastic Fiber Assembly and Its Perturbation in Pulmonary Arterial Hypertension

被引:41
|
作者
Tojais, Nancy F. [1 ]
Cao, Aiqin [1 ]
Lai, Ying-Ju [1 ,5 ]
Wang, Lingli [1 ]
Chen, Pin-I [1 ]
Alcazar, Miguel A. Alejandre [1 ,6 ]
Perez, Vinicio A. de Jesus [2 ,3 ]
Hopper, Rachel K. [1 ,7 ,8 ]
Rhodes, Christopher J. [1 ,9 ]
Bill, Matthew A. [2 ,3 ]
Sakai, Lynn Y. [4 ]
Rabinovitch, Marlene [1 ]
机构
[1] Stanford Univ, Dept Pediat, Sch Med, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Med, Vera Moulton Wall Ctr Pulm Vasc Dis, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Cardiovasc Inst, Stanford, CA USA
[4] Oregon Hlth & Sci Univ, Shriners Hosp Children, Portland, OR 97201 USA
[5] Chang Gung Univ, Coll Med, Dept Resp Therapy, Taoyuan, Taiwan
[6] Univ Hosp Cologne, Dept Pediat, Cologne, Germany
[7] Univ Penn, Dept Pediat, Perelman Sch Med, Philadelphia, PA 19104 USA
[8] Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA
[9] Imperial Coll London, Hammersmith Hosp, London, England
基金
美国国家卫生研究院;
关键词
BMPR2; receptor; elastin; fibrillin-1; fibroblasts; hypertension; pulmonary; smooth muscle cells; TGF-beta-1; SMOOTH-MUSCLE-CELLS; MARFAN-SYNDROME; ENDOTHELIAL DYSFUNCTION; IN-VITRO; BMPR2; FIBRILLIN; MICE; GENE; EXPRESSION; MUTATIONS;
D O I
10.1161/ATVBAHA.117.309696
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective-We determined in patients with pulmonary arterial (PA) hypertension (PAH) whether in addition to increased production of elastase by PA smooth muscle cells previously reported, PA elastic fibers are susceptible to degradation because of their abnormal assembly. Approach and Results-Fibrillin-1 and elastin are the major components of elastic fibers, and fibrillin-1 binds bone morphogenetic proteins (BMPs) and the large latent complex of transforming growth factor-beta 1 (TGF beta 1). Thus, we considered whether BMPs like TGF beta 1 contribute to elastic fiber assembly and whether this process is perturbed in PAH particularly when the BMP receptor, BMPR2, is mutant. We also assessed whether in mice with Bmpr2/1a compound heterozygosity, elastic fibers are susceptible to degradation. In PA smooth muscle cells and adventitial fibroblasts, TGF beta 1 increased elastin mRNA, but the elevation in elastin protein was dependent on BMPR2; TGF beta 1 and BMP4, via BMPR2, increased extracellular accumulation of fibrillin-1. Both BMP4-and TGF beta 1-stimulated elastic fiber assembly was impaired in idiopathic (I) PAH-PA adventitial fibroblast versus control cells, particularly those with hereditary (H) PAH and a BMPR2 mutation. This was related to profound reductions in elastin and fibrillin-1 mRNA. Elastin protein was increased in IPAH PA adventitial fibroblast by TGF beta 1 but only minimally so in BMPR2 mutant cells. Fibrillin-1 protein increased only modestly in IPAH or HPAH PA adventitial fibroblasts stimulated with BMP4 or TGF beta 1. In Bmpr2/1a heterozygote mice, reduced PA fibrillin-1 was associated with elastic fiber susceptibility to degradation and more severe pulmonary hypertension. Conclusions-Disrupting BMPR2 impairs TGF beta 1-and BMP4-mediated elastic fiber assembly and is of pathophysiologic significance in PAH. Visual Overview-An online visual overview is available for this article.
引用
收藏
页码:1559 / +
页数:28
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