Bartlett Paula J, Gaspers Lawrence D, Pierobon Nicola, Thomas Andrew P
Department of Pharmacology and Physiology, New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, NJ, USA.
Department of Pharmacology and Physiology, New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, NJ, USA.
Cell Calcium. 2014 Jun;55(6):306-16. doi: 10.1016/j.ceca.2014.02.007. Epub 2014 Feb 17.
A major role of the liver is to integrate multiple signals to maintain normal blood glucose levels. The balance between glucose storage and mobilization is primarily regulated by the counteracting effects of insulin and glucagon. However, numerous signals converge in the liver to ensure energy demand matches the physiological status of the organism. Many circulating hormones regulate glycogenolysis, gluconeogenesis and mitochondrial metabolism by calcium-dependent signaling mechanisms that manifest as cytosolic Ca(2+) oscillations. Stimulus-strength is encoded in the Ca(2+) oscillation frequency, and also by the range of intercellular Ca(2+) wave propagation in the intact liver. In this article, we describe how Ca(2+) oscillations and waves can regulate glucose output and oxidative metabolism in the intact liver; how multiple stimuli are decoded though Ca(2+) signaling at the organ level, and the implications of Ca(2+) signal dysregulation in diseases such as metabolic syndrome and non-alcoholic fatty liver disease.
肝脏的一个主要作用是整合多种信号以维持正常的血糖水平。葡萄糖储存与动员之间的平衡主要受胰岛素和胰高血糖素的拮抗作用调节。然而,众多信号在肝脏中汇聚,以确保能量需求与机体的生理状态相匹配。许多循环激素通过钙依赖性信号机制调节糖原分解、糖异生和线粒体代谢,这些机制表现为胞质Ca(2+)振荡。刺激强度由Ca(2+)振荡频率编码,也由完整肝脏中细胞间Ca(2+)波传播的范围编码。在本文中,我们描述了Ca(2+)振荡和波如何调节完整肝脏中的葡萄糖输出和氧化代谢;多种刺激如何在器官水平通过Ca(2+)信号进行解码,以及Ca(2+)信号失调在代谢综合征和非酒精性脂肪性肝病等疾病中的影响。