DAN plays important compensatory roles in systemic‐to‐pulmonary shunt associated pulmonary arterial hypertension

医学 BMPR2型 肺动脉高压 血流动力学 内科学 肺动脉 心脏病学 胚胎血管重塑 缺氧性肺血管收缩 心导管术 分流(医疗) 内分泌学 病理 骨形态发生蛋白 生物 基因 生物化学
作者
Liukun Meng,Xiaoyan Liu,Xiao Teng,Wen Yuan,Lihua Duan,Jian Meng,Jun Li,Zhe Zheng,Yingjie Wei,Shengshou Hu
出处
期刊:Acta Physiologica [Wiley]
卷期号:226 (3) 被引量:6
标识
DOI:10.1111/apha.13263
摘要

Abstract Aim Proteins mainly expressed in normal lungs and significantly changed in lungs exposed to systemic‐to‐pulmonary shunts might be promising targets for pulmonary arterial hypertension induced by congenital heart diseases (PAH/CHD). This study aimed to investigate the potential role of differential screening‐selected gene aberrative in neuroblastoma (DAN) in PAH/CHD. Methods PAH was surgically induced by the combined surgery (right pulmonary artery ligation and left cervical systemic‐to‐pulmonary shunt) in Sprague‐Dawley (SD) rats. Exogenous DAN was supplemented by osmotic minipumps. Results Firstly, DAN was significantly decreased in patients with severe PAH/CHD and negatively correlated with pulmonary hemodynamic indices derived from right cardiac catheterization. Secondly, pulmonary hypertensive status and apparent pulmonary vasculopathies of PAH/CHD were surgically reproduced in SD rats. Real time‐PCR and Western blot analysis revealed that DAN mRNA and protein levels decreased in lungs exposed to systemic‐to‐pulmonary shunts, and immunofluorescence staining found that DAN was highly expressed in pulmonary arteries of normal lungs but seldom detected in severely remodelling pulmonary arteries, furthermore, plasma levels of DAN in shunted‐rats manifested a time‐depended decrease and negatively correlated with pulmonary hemodynamic indices. Thirdly, DAN specially reversed the anti‐proliferative and pro‐apoptotic effects of bone morphogenetic protein 2/4 (BMP2/4) on pulmonary arterial smooth muscle cells via BMP2/4‐BMPR2‐Smad1/5/8‐Id1 signalling pathway. Furthermore, continuous supplementation of exogenous DAN protein increased the extent of shunt‐associated PAH. Conclusion Compensatory decrease of DAN in hypertensive lungs may retard the deterioration of shunt‐associated PAH, at least in part, by antagonizing BMP signalling pathway. Furthermore, DAN might be a potential biomarker for PAH/CHD.

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