Scimia Maria Cecilia, Blass Benjamin E, Koch Walter J
Temple University School of Medicine, Philadelphia, PA, USA.
Expert Rev Cardiovasc Ther. 2014 Jun;12(6):733-41. doi: 10.1586/14779072.2014.911661. Epub 2014 May 5.
It has recently been demonstrated that the apelin receptor (APJ) plays a significant role in mediating the stretch response within the heart in a G-protein-independent and β-arrestin-dependent fashion. This discovery adds to the consolidated literature describing the potential benefits of APJ agonists. In this review, the authors will examine the functional selectivity of APJ and stretch with respect to their ability to signal via both G-protein-dependent and G-protein-independent mechanisms, with a focus on the multifunctional protein, β-arrestin. The possibility of selecting or designing novel ligands that differentially activate only a subset of functions via a single receptor holds great promise for the treatment of diseases such as heart failure and hypertension. Finally, hypothetical approaches to target APJ, taking into account its downstream pathways, will be described.
最近有研究表明,阿片肽受体(APJ)在介导心脏的牵张反应中发挥着重要作用,其作用方式不依赖G蛋白,而是依赖β - 抑制蛋白。这一发现为描述APJ激动剂潜在益处的大量文献增添了新内容。在这篇综述中,作者将研究APJ和牵张在通过G蛋白依赖和G蛋白非依赖机制进行信号传导方面的功能选择性,重点关注多功能蛋白β - 抑制蛋白。通过单一受体选择性激活或设计仅能激活部分功能的新型配体,对于治疗心力衰竭和高血压等疾病具有巨大潜力。最后,将描述考虑到APJ下游通路的靶向APJ的假设方法。