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铁调素是肾素活性的潜在调节剂。

Hepcidin is potential regulator for renin activity.

机构信息

Facult of Medicine and Health Technology, Tampere University, Tampere, Finland.

Patendo Oy, Parainen, Finland.

出版信息

PLoS One. 2022 Apr 20;17(4):e0267343. doi: 10.1371/journal.pone.0267343. eCollection 2022.

Abstract

An association between genetic variants in the genes HFE, HJV, BMP4 and arterial hypertension has been shown earlier. Proteins encoded by these genes participate in the signalling routes leading eventually to the production of the peptide hormone hepcidin. Mutations in these genes have been associated with the abnormal production of hepcidin in the body. This finding led to studies exploring the possible role of hepcidin in regulating the activity of blood pressure related renin-angiotensin system enzymes. We used molecular modelling to find out if it is possible for hepcidin to bind to the active site of the renin-angiotensin system enzymes, especially renin. Fluorometric assays were used to evaluate the inhibitory effect of hepcidin on renin as well as angiotensin converting enzymes 1 and 2. Finally, bio-layer interferometry technique was used to study hepcidin binding to renin. The molecular modelling showed that hepcidin seems to have similar binding properties to the renin active site as angiotensinogen does. Based on fluorometric enzyme activity assay, hepcidin has an inhibitory effect on renin in vitro, too. However, angiotensin converting enzymes 1 and 2 were not inhibited remarkably by hepcidin-25. In bio-layer interferometry analysis hepcidin-renin binding was concentration dependent. Our results suggest that hepcidin could act as an inhibitor to the renin. Nowadays, there is no known biological inhibitor for renin in vivo and our finding may thus have important clinical implications.

摘要

先前已有研究表明,基因 HFE、HJV 和 BMP4 中的遗传变异与动脉高血压之间存在关联。这些基因编码的蛋白质参与了最终导致肽激素铁调素产生的信号通路。这些基因的突变与体内铁调素的异常产生有关。这一发现促使人们研究铁调素在调节与血压相关的肾素-血管紧张素系统酶活性方面的可能作用。我们使用分子建模来确定铁调素是否有可能与肾素-血管紧张素系统酶(特别是肾素)的活性位点结合。荧光测定法用于评估铁调素对肾素以及血管紧张素转换酶 1 和 2 的抑制作用。最后,使用生物层干涉技术研究铁调素与肾素的结合。分子建模表明,铁调素似乎具有与肾素活性位点相似的结合特性,就像血管紧张素原一样。根据荧光酶活性测定,铁调素在体外对肾素有抑制作用。然而,铁调素-25 对血管紧张素转换酶 1 和 2 的抑制作用并不明显。在生物层干涉分析中,铁调素-肾素结合具有浓度依赖性。我们的结果表明,铁调素可以作为肾素的抑制剂。目前,体内尚未发现已知的肾素生物抑制剂,因此我们的发现可能具有重要的临床意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c03c/9020709/f82b15382ac0/pone.0267343.g001.jpg

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