Calcium-dependent regulation of glucose homeostasis in the liver

被引:92
作者
Bartlett, Paula J. [1 ]
Gaspers, Lawrence D. [1 ]
Pierobon, Nicola [1 ]
Thomas, Andrew P. [1 ]
机构
[1] Rutgers State Univ, New Jersey Med Sch, Dept Physiol & Pharmacol, Newark, NJ 07102 USA
关键词
Calcium; Hepatocyte; Mitochondrial metabolism; Glucose homeostasis; IP3; receptor; Metabolic syndrome; Liver; PROTEIN-KINASE-C; INOSITOL 1,4,5-TRISPHOSPHATE RECEPTORS; ENDOPLASMIC-RETICULUM STRESS; CYTOPLASMIC FREE CALCIUM; ISOLATED RAT HEPATOCYTES; CA2+ RELEASE CHANNELS; INSULIN-RESISTANCE; GENE-EXPRESSION; PERFUSED LIVER; INTACT LIVER;
D O I
10.1016/j.ceca.2014.02.007
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
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 Ca2+ oscillations. Stimulus-strength is encoded in the Ca2+ oscillation frequency, and also by the range of intercellular Ca2+ wave propagation in the intact liver. In this article, we describe how Ca2+ oscillations and waves can regulate glucose output and oxidative metabolism in the intact liver; how multiple stimuli are decoded though Ca2+ signaling at the organ level, and the implications of Ca2+ signal dysregulation in diseases such as metabolic syndrome and non-alcoholic fatty liver disease. (C) 2014 Published by Elsevier Ltd.
引用
收藏
页码:306 / 316
页数:11
相关论文
共 136 条
[1]
Calcium Signaling in the Liver [J].
Amaya, Maria Jimena ;
Nathanson, Michael H. .
COMPREHENSIVE PHYSIOLOGY, 2013, 3 (01) :515-539
[2]
SIMULTANEOUS RECORDING OF MEMBRANE POTENTIAL CALCIUM TRANSIENT AND TENSION IN SINGLE MUSCLE FIBRES [J].
ASHLEY, CC ;
RIDGWAY, EB .
NATURE, 1968, 219 (5159) :1168-&
[3]
Single cell analysis and temporal profiling of agonist-mediated inositol 1,4,5-trisphosphate, Ca2+, diacylglycerol, and protein kinase C signaling using fluorescent biosensors [J].
Bartlett, PJ ;
Young, KW ;
Nahorski, SR ;
Challiss, RAJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (23) :21837-21846
[4]
Integrative genomics identifies MCU as an essential component of the mitochondrial calcium uniporter [J].
Baughman, Joshua M. ;
Perocchi, Fabiana ;
Girgis, Hany S. ;
Plovanich, Molly ;
Belcher-Timme, Casey A. ;
Sancak, Yasemin ;
Bao, X. Robert ;
Strittmatter, Laura ;
Goldberger, Olga ;
Bogorad, Roman L. ;
Koteliansky, Victor ;
Mootha, Vamsi K. .
NATURE, 2011, 476 (7360) :341-U111
[5]
The interaction of hepatic lipid and glucose metabolism in liver diseases [J].
Bechmann, Lars P. ;
Hannivoort, Rebekka A. ;
Gerken, Guido ;
Hotamisligil, Goekhan S. ;
Trauner, Michael ;
Canbay, Ali .
JOURNAL OF HEPATOLOGY, 2012, 56 (04) :952-964
[6]
Bernard C., 1854, LECONS PHYSICLOGIE E
[7]
The versatility and universality of calcium signalling [J].
Berridge, MJ ;
Lipp, P ;
Bootman, MD .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2000, 1 (01) :11-21
[8]
CYTOSOLIC CALCIUM OSCILLATORS [J].
BERRIDGE, MJ ;
GALIONE, A .
FASEB JOURNAL, 1988, 2 (15) :3074-3082
[9]
BERRIE CP, 1995, CELL CALCIUM, V18, P232, DOI 10.1016/0143-4160(95)90068-3
[10]
Protein Kinase A Increases Type-2 Inositol 1,4,5-Trisphosphate Receptor Activity by Phosphorylation of Serine 937 [J].
Betzenhauser, Matthew J. ;
Fike, Jenna L. ;
Wagner, Larry E., II ;
Yule, David I. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (37) :25116-25125