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强心甾体对 Na/K-ATPase 介导的信号转导的偏倚效应。

Biased Effect of Cardiotonic Steroids on Na/K-ATPase-Mediated Signal Transduction.

机构信息

Marshall Institute for Interdisciplinary Research, Huntington, West Virginia (Y.X., P.M., M.H., T.W., L.C., Z.X.); University of Toledo College of Medicine and Life Sciences, Toledo, Ohio (J.X.X.); Joan C. Edwards School of Medicine at Marshall University, Huntington, West Virginia (J.I.S.); and Department of Natural Medicinal Chemistry, China Pharmaceutical University, Nanjing, P. R. China, and Jiangsu Food and Pharmaceutical Science College, Huai'an, P. R. China (F.F.)

Marshall Institute for Interdisciplinary Research, Huntington, West Virginia (Y.X., P.M., M.H., T.W., L.C., Z.X.); University of Toledo College of Medicine and Life Sciences, Toledo, Ohio (J.X.X.); Joan C. Edwards School of Medicine at Marshall University, Huntington, West Virginia (J.I.S.); and Department of Natural Medicinal Chemistry, China Pharmaceutical University, Nanjing, P. R. China, and Jiangsu Food and Pharmaceutical Science College, Huai'an, P. R. China (F.F.).

出版信息

Mol Pharmacol. 2021 Mar;99(3):217-225. doi: 10.1124/molpharm.120.000101. Epub 2021 Jan 25.

Abstract

Recent studies have revealed that Na/K-ATPase (NKA) can transmit signals through ion-pumping-independent activation of pathways relayed by distinct intracellular protein/lipid kinases, and endocytosis challenges the traditional definition that cardiotonic steroids (CTS) are NKA inhibitors. Although additional effects of CTS have long been suspected, revealing its agonist impact through the NKA receptor could be a novel mechanism in understanding the basic biology of NKA. In this study, we tested whether different structural CTS could trigger different sets of NKA/effector interactions, resulting in biased signaling responses without compromising ion-pumping capacity. Using purified NKA, we found that ouabain, digitoxigenin, and somalin cause comparable levels of NKA inhibition. However, although endogenous ouabain stimulates both protein kinases and NKA endocytosis, digitoxigenin and somalin bias to protein kinases and endocytosis, respectively, in LLC-PK1 cells. The positive inotropic effects of CTS are traditionally regarded as NKA inhibitors. However, CTS-induced signaling occurs at concentrations at least one order of magnitude lower than that of inotropy, which eliminates their well known toxic actions on the heart. The current study adds a novel mechanism that CTS could exert its biased signaling properties through the NKA signal transducer. SIGNIFICANCE STATEMENT: Although it is now well accepted that NKA has an ion-pumping-independent signaling function, it is still debated whether direct and conformation-dependent NKA/effector interaction is a key to this function. Therefore, this investigation is significant in advancing our understanding of the basic biology of NKA-mediated signal transduction and gaining molecular insight into the structural elements that are important for cardiotonic steroid's biased action.

摘要

最近的研究表明,Na/K-ATP 酶(NKA)可以通过离子泵非依赖性激活由不同的细胞内蛋白/脂质激酶传递的途径来传递信号,内吞作用挑战了强心甾(CTS)是 NKA 抑制剂的传统定义。尽管长期以来人们一直怀疑 CTS 具有其他作用,但通过 NKA 受体揭示其激动剂作用可能是理解 NKA 基本生物学的一种新机制。在这项研究中,我们测试了不同结构的 CTS 是否可以触发不同的 NKA/效应器相互作用集,从而在不损害离子泵功能的情况下产生偏向信号反应。使用纯化的 NKA,我们发现哇巴因、地高辛和 somalin 引起的 NKA 抑制水平相当。然而,尽管内源性哇巴因刺激蛋白激酶和 NKA 内吞作用,但地高辛和 somalin 分别偏向蛋白激酶和内吞作用。CTS 的正性肌力作用传统上被认为是 NKA 抑制剂。然而,CTS 诱导的信号发生在浓度至少低一个数量级,这消除了它们对心脏的已知毒性作用。本研究增加了一种新的机制,即 CTS 可以通过 NKA 信号转导器发挥其偏向信号特性。意义声明:尽管现在人们普遍接受 NKA 具有离子泵非依赖性的信号功能,但仍然存在争议,即直接和构象依赖性的 NKA/效应器相互作用是否是该功能的关键。因此,这项研究对于深入了解 NKA 介导的信号转导的基本生物学以及深入了解对强心甾偏向作用重要的结构元素具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3874/7919863/f3fa993d0b27/molpharm.120.000101absf1.jpg

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