Increased kielin/chordin-like protein levels are associated with the severity of heart failure

内科学 心力衰竭 医学 射血分数 扩张型心肌病 心钠素 心脏病学 脑利钠肽 内分泌学 骨形态发生蛋白 骨形态发生蛋白2 肥厚性心肌病 骨形态发生蛋白7 利钠肽 脂联素 生物 胰岛素 胰岛素抵抗 体外 基因 生物化学
作者
Jing Ye,Zhen Wang,Menglong Wang,Yao Xu,Tao Zeng,Di Ye,Jianfang Liu,Huimin Jiang,Yingzhong Lin,Jun Wan
出处
期刊:Clinica Chimica Acta [Elsevier BV]
卷期号:486: 381-386 被引量:7
标识
DOI:10.1016/j.cca.2018.08.033
摘要

Previous studies demonstrated that the transforming growth factor (TGF) β superfamily, including TGF-βs and bone morphogenetic proteins (BMPs), plays important roles in cardiovascular diseases. The kielin/chordin-like protein (KCP) is a secreted protein that regulates the expression and function of TGF-βs and BMPs. However, the role of KCP during heart failure (HF) remains unknown. The present study aimed to investigate the cardiac expression of KCP in human failing hearts.The human failing heart samples from patients with dilated cardiomyopathy (DCM, n = 12) and ischemic cardiomyopathy (ICM, n = 12) were collected, and normal heart (n = 8) samples from unmatched donors were collected as controls. Collagen volume, KCP levels, and mRNA levels of several BMPs in left ventricles (LV) of all hearts were measured.The KCP levels were significantly higher in human failing hearts than in normal hearts. KCP levels were positively associated with hypertrophy markers, including atrial natriuretic peptide (ANP), brain natriuretic peptide (BNP) and β-myosin heavy chain (β-MHC). In addition, KCP levels were also positively associated with left ventricular end-diastolic dimension (LVEDD), collagen Iα and collagen IIIα expression but were negatively associated with left ventricular ejection fraction (LVEF). Furthermore, increased TGF-β1, BMP2/4/6/10 and reduced BMP7 levels were observed, and positive correlations between KCP and TGF-β1 and negative correlation between KCP and BMP2/7 were found, but not for BMP4/6/10.KCP was closely associated with heart failure. The regulation of BMP2/7 and TGF-β1 expression may be the possible mechanisms.

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