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中链脂肪酸通过一种心脏气味受体调节心肌功能。

Medium-chain fatty acids modulate myocardial function via a cardiac odorant receptor.

作者信息

Jovancevic Nikolina, Dendorfer A, Matzkies M, Kovarova M, Heckmann J C, Osterloh M, Boehm M, Weber L, Nguemo F, Semmler J, Hescheler J, Milting H, Schleicher E, Gelis L, Hatt H

机构信息

Department of Cell Physiology, Ruhr-University Bochum, 44801, Bochum, Germany.

Walter Brendel Centre of Experimental Medicine, Ludwig-Maximilians-University, 80336, Munich, Germany.

出版信息

Basic Res Cardiol. 2017 Mar;112(2):13. doi: 10.1007/s00395-017-0600-y. Epub 2017 Jan 23.

Abstract

Several studies have demonstrated the expression of odorant receptors (OR) in various human tissues and their involvement in different physiological and pathophysiological processes. However, the functional role of ORs in the human heart is still unclear. Here, we firstly report the functional characterization of an OR in the human heart. Initial next-generation sequencing analysis revealed the OR expression pattern in the adult and fetal human heart and identified the fatty acid-sensing OR51E1 as the most highly expressed OR in both cardiac development stages. An extensive characterization of the OR51E1 ligand profile by luciferase reporter gene activation assay identified 2-ethylhexanoic acid as a receptor antagonist and various structurally related fatty acids as novel OR51E1 ligands, some of which were detected at receptor-activating concentrations in plasma and epicardial adipose tissue. Functional investigation of the endogenous receptor was carried out by Ca imaging of human stem cell-derived cardiomyocytes. Application of OR51E1 ligands induced negative chronotropic effects that depended on activation of the OR. OR51E1 activation also provoked a negative inotropic action in cardiac trabeculae and slice preparations of human explanted ventricles. These findings indicate that OR51E1 may play a role as metabolic regulator of cardiac function.

摘要

多项研究已证实气味受体(OR)在人体各种组织中的表达及其参与不同的生理和病理生理过程。然而,OR在人类心脏中的功能作用仍不清楚。在此,我们首次报道了人类心脏中一种OR的功能特性。最初的新一代测序分析揭示了成人和胎儿心脏中的OR表达模式,并确定脂肪酸感应OR51E1是两个心脏发育阶段中表达最高的OR。通过荧光素酶报告基因激活试验对OR51E1配体谱进行的广泛表征确定2-乙基己酸为受体拮抗剂,各种结构相关的脂肪酸为新型OR51E1配体,其中一些在血浆和心外膜脂肪组织中以受体激活浓度被检测到。通过对人干细胞衍生的心肌细胞进行钙成像对内源性受体进行了功能研究。应用OR51E1配体可诱导负性变时效应,这取决于OR的激活。OR51E1激活还可在心脏小梁和人离体心室切片标本中引发负性变力作用。这些发现表明OR51E1可能作为心脏功能的代谢调节因子发挥作用。

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