Hardy-Rando Eugenio, Fernandez-Patron Carlos
Biotechnology Laboratory, Study Center for Research and Biological Evaluations, Institute of Pharmacy and Foods, University of Havana, Havana PO Box 430, Cuba.
Department of Biochemistry, Cardiovascular Research Centre, Mazankowski Alberta Heart Institute, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, AB T6G 2H7, Canada.
J Biomed Res. 2019 Jun 4;33(3):145-155. doi: 10.7555/JBR.32.20170137.
The breakthrough discovery of cardiac natriuretic peptides provided the first direct demonstration of the connection between the heart and the kidneys for the maintenance of sodium and volume homeostasis in health and disease. Yet, little is still known about how the heart and other organs cross-talk. Here, we review three physiological mechanisms of communication linking the heart to other organs through: i) cardiac natriuretic peptides, ii) the microRNA-208a/mediator complex subunit-13 axis and iii) the matrix metalloproteinase-2 (MMP-2)/C-C motif chemokine ligand-7/cardiac secreted phospholipase A2 (sPLA2) axis - a pathway which likely applies to the many cytokines, which are cleaved and regulated by MMP-2. We also suggest experimental strategies to answer still open questions on the latter pathway. In short, we review evidence showing how the cardiac secretome influences the metabolic and inflammatory status of non-cardiac organs as well as the heart.
心脏利钠肽的突破性发现首次直接证明了在健康和疾病状态下,心脏与肾脏之间在维持钠和容量稳态方面的联系。然而,关于心脏与其他器官如何相互作用,我们仍然知之甚少。在这里,我们回顾了三种将心脏与其他器官联系起来的生理通讯机制:i)心脏利钠肽,ii)微小RNA-208a/介质复合物亚基-13轴,以及iii)基质金属蛋白酶-2(MMP-2)/C-C基序趋化因子配体-7/心脏分泌型磷脂酶A2(sPLA2)轴——这一途径可能适用于许多由MMP-2切割和调节的细胞因子。我们还提出了实验策略,以回答关于后一途径的仍未解决的问题。简而言之,我们回顾了相关证据,展示了心脏分泌组如何影响非心脏器官以及心脏的代谢和炎症状态。