Marcelo Kathrina L, Means Anthony R, York Brian
Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX, USA.
Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX, USA; Dan L. Duncan Cancer Center, Baylor College of Medicine, Houston, TX, USA.
Trends Endocrinol Metab. 2016 Oct;27(10):706-718. doi: 10.1016/j.tem.2016.06.001. Epub 2016 Jul 20.
Calcium (Ca(2+)) is an essential ligand that binds its primary intracellular receptor calmodulin (CaM) to trigger a variety of downstream processes and pathways. Central to the actions of Ca(2+)/CaM is the activation of a highly conserved Ca(2+)/CaM kinase (CaMK) cascade that amplifies Ca(2+) signals through a series of subsequent phosphorylation events. Proper regulation of Ca(2+) flux is necessary for whole-body metabolism and disruption of Ca(2+) homeostasis has been linked to various metabolic diseases. Here we provide a synthesis of recent advances that highlight the roles of the Ca(2+)/CaMK axis in key metabolic tissues. An appreciation of this information is critical to understanding the mechanisms by which Ca(2+)/CaM-dependent signaling contributes to metabolic homeostasis and disease.
钙(Ca(2+))是一种必需的配体,它与其主要的细胞内受体钙调蛋白(CaM)结合,以触发各种下游过程和途径。Ca(2+)/CaM作用的核心是激活高度保守的Ca(2+)/CaM激酶(CaMK)级联反应,该反应通过一系列后续的磷酸化事件放大Ca(2+)信号。Ca(2+)通量的适当调节对于全身代谢是必要的,而Ca(2+)稳态的破坏与各种代谢疾病有关。在这里,我们综述了最近的进展,突出了Ca(2+)/CaMK轴在关键代谢组织中的作用。了解这些信息对于理解Ca(2+)/CaM依赖性信号传导促进代谢稳态和疾病的机制至关重要。