The complex interplay in the regulation of cardiac pathophysiologic functionalities by protein kinases and phosphatases

Chukwuma Sr Chrysanthus
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引用次数: 2

Abstract

Protein phosphorylation regulates several dimensions of cell fate and is substantially dysregulated in pathophysiological instances as evident spatiotemporally via intracellular localizations or compartmentalizations with discrete control by specific kinases and phosphatases. Cardiovascular disease manifests as an intricately complex entity presenting as a derangement of the cardiovascular system. Cardiac or heart failure connotes the pathophysiological state in which deficient cardiac output compromises the body burden and requirements. Protein kinases regulate several pathophysiological processes and are emerging targets for drug lead or discovery. The protein kinases are family members of the serine/threonine phosphatases. Protein kinases covalently modify proteins by attaching phosphate groups from ATP to residues of serine, threonine and/or tyrosine. Protein kinases and phosphatases are pivotal in the regulatory mechanisms in the reversible phosphorylation of diverse effectors whereby discrete signaling molecules regulate cardiac excitation and contraction. Protein phosphorylation is critical for the sustenance of cardiac functionalities. The two major contributory ingredients to progressive myocardium derangement are dysregulation of Ca2+ processes and contemporaneous elevated concentrations of reactive oxygen species, ROS. Certain cardiac abnormalities include cardiac myopathy or hypertrophy due to response in untoward haemodynamic demand with concomitant progressive heart failure. The homeostasis or equilibrium between protein kinases and phosphatases influence cardiac morphology and excitability during pathological and physiological processes of the cardiovascular system. Inasmuch as protein kinases regulate numerous dimensions of normal cellular functions, the pathophysiological dysfunctionality of protein kinase signaling pathways undergirds the molecular aspects of several cardiovascular diseases or disorders as related in this study. These have presented protein kinases as essential and potential targets for drug discovery and heart disease therapy.
蛋白激酶和磷酸酶在心脏病理生理功能调节中的复杂相互作用
蛋白质磷酸化调节细胞命运的几个方面,并且在病理生理学情况下显著失调,这在时空上是明显的,通过特定激酶和磷酸酶的离散控制进行细胞内定位或区隔。心血管疾病表现为一个复杂的实体,表现为心血管系统紊乱。心力衰竭意味着心输出量不足会损害身体负担和需求的病理生理状态。蛋白激酶调节几种病理生理过程,是药物开发或发现的新靶点。蛋白激酶是丝氨酸/苏氨酸磷酸酶的家族成员。蛋白激酶通过将ATP的磷酸基团连接到丝氨酸、苏氨酸和/或酪氨酸的残基上来共价修饰蛋白质。蛋白激酶和磷酸酶在多种效应物可逆磷酸化的调节机制中起关键作用,通过这些机制,离散的信号分子调节心脏兴奋和收缩。蛋白质磷酸化对维持心脏功能至关重要。进行性心肌紊乱的两个主要因素是Ca2+过程的失调和同时升高的活性氧(ROS)浓度。某些心脏异常包括由于对不良血液动力学需求的反应而引起的心肌病或肥大,并伴有进行性心力衰竭。蛋白激酶和磷酸酶之间的稳态或平衡在心血管系统的病理和生理过程中影响心脏形态和兴奋性。由于蛋白激酶调节正常细胞功能的许多方面,蛋白激酶信号通路的病理生理功能障碍是本研究中几种心血管疾病或病症的分子方面的基础。这些已经表明蛋白激酶是药物发现和心脏病治疗的重要和潜在靶点。
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