Parra Valentina, Rothermel Beverly A
Advanced Centre for Chronic Disease (ACCDiS), Facultad Ciencias Quimicas y Farmaceuticas, Universidad de Chile, Santiago,Chile; Departamento de Bioquímica y Biología Molecular, Facultad de Ciencias Quimicas y Farmaceuticas, Universidad de Chie, Santiago, Chile.
Department of Internal Medicine (Cardiology Division), University of Texas Southwestern Medical Centre, Dallas, TX, USA; Department of Molecular Biology, University of Texas Southwestern Medical Centre, Dallas, TX, USA.
J Mol Cell Cardiol. 2017 Feb;103:121-136. doi: 10.1016/j.yjmcc.2016.12.006. Epub 2016 Dec 20.
The calcium-activated protein phosphatase, calcineurin, lies at the intersection of protein phosphorylation and calcium signaling cascades, where it provides an essential nodal point for coordination between these two fundamental modes of intracellular communication. In excitatory cells, such as neurons and cardiomyocytes, that experience rapid and frequent changes in cytoplasmic calcium, calcineurin protein levels are exceptionally high, suggesting that these cells require high levels of calcineurin activity. Yet, it is widely recognized that excessive activation of calcineurin in the heart contributes to pathological hypertrophic remodeling and the progression to failure. How does a calcium activated enzyme function in the calcium-rich environment of the continuously contracting heart without pathological consequences? This review will discuss the wide range of calcineurin substrates relevant to cardiovascular health and the mechanisms calcineurin uses to find and act on appropriate substrates in the appropriate location while potentially avoiding others. Fundamental differences in calcineurin signaling in neonatal verses adult cardiomyocytes will be addressed as well as the importance of maintaining heterogeneity in calcineurin activity across the myocardium. Finally, we will discuss how circadian oscillations in calcineurin activity may facilitate integration with other essential but conflicting processes, allowing a healthy heart to reap the benefits of calcineurin signaling while avoiding the detrimental consequences of sustained calcineurin activity that can culminate in heart failure.
钙激活蛋白磷酸酶钙调神经磷酸酶处于蛋白质磷酸化和钙信号级联反应的交叉点,在这两种基本的细胞内通讯模式之间的协调中提供了一个关键节点。在经历细胞质钙快速频繁变化的兴奋性细胞,如神经元和心肌细胞中,钙调神经磷酸酶的蛋白水平异常高,这表明这些细胞需要高水平的钙调神经磷酸酶活性。然而,人们普遍认识到,心脏中钙调神经磷酸酶的过度激活会导致病理性肥厚重塑和心力衰竭的进展。在持续收缩的心脏富含钙的环境中,一种钙激活酶如何发挥作用而不产生病理后果呢?本综述将讨论与心血管健康相关的多种钙调神经磷酸酶底物,以及钙调神经磷酸酶在合适位置找到并作用于合适底物同时可能避开其他底物所采用的机制。还将探讨新生与成年心肌细胞中钙调神经磷酸酶信号传导的根本差异,以及维持心肌中钙调神经磷酸酶活性异质性的重要性。最后,我们将讨论钙调神经磷酸酶活性的昼夜振荡如何促进与其他重要但相互冲突的过程的整合,使健康的心脏能够在避免持续的钙调神经磷酸酶活性可能导致心力衰竭的有害后果的同时,从钙调神经磷酸酶信号传导中获益。