Novel insights into ChREBP regulation and function

被引:166
作者
Filhoulaud, Gaelle [1 ,2 ,3 ]
Guilmeau, Sandra [1 ,2 ,3 ]
Dentin, Renaud [1 ,2 ,3 ]
Girard, Jean [1 ,2 ,3 ]
Postic, Catherine [1 ,2 ,3 ]
机构
[1] Inst Cochin Genet Mol, INSERM, U1016, F-75014 Paris, France
[2] CNRS, UMR8104, Paris, France
[3] Univ Paris 05, Paris, France
关键词
ChREBP; glucose sensing; hepatic steatosis; beta cell glucotoxicity; cell proliferation; CARBOHYDRATE RESPONSE ELEMENT; THIOREDOXIN-INTERACTING PROTEIN; PYRUVATE-KINASE GENE; FATTY-ACID-SYNTHASE; CENTER-DOT-MLX; BINDING-PROTEIN; TRANSCRIPTION FACTOR; ADIPOSE-TISSUE; INSULIN-RESISTANCE; HEPATIC STEATOSIS;
D O I
10.1016/j.tem.2013.01.003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Glucose is an energy source that also controls the expression of key genes involved in energetic metabolism through the glucose-signaling transcription factor carbohydrate response element-binding protein (ChREBP). ChREBP has recently emerged as a central regulator of glycolysis and de novo fatty acid synthesis in liver, but new evidence shows that it plays a broader and crucial role in various processes, ranging from glucolipotoxicity to apoptosis and/or proliferation in specific cell types. However, several aspects of ChREBP activation by glucose metabolites are currently controversial, as well as the effects of activating or inhibiting ChREBP, on insulin sensitivity, which might depend on genetic, dietary or environmental factors. Thus, much remains to be elucidated. Here, we summarize our current understanding of the regulation and function of this fascinating transcription factor.
引用
收藏
页码:257 / 268
页数:12
相关论文
共 97 条
[1]   FGF21: The Center of a Transcriptional Nexus in Metabolic Regulation [J].
Adams, A. C. ;
Kharitonenkov, A. .
CURRENT DIABETES REVIEWS, 2012, 8 (04) :285-293
[2]   Glucose 6-phosphate regulates hepatic glycogenolysis through inactivation of phosphorylase [J].
Aiston, S ;
Andersen, B ;
Agius, L .
DIABETES, 2003, 52 (06) :1333-1339
[3]   Fructose 2,6-bisphosphate is essential for glucose-regulated gene transcription of glucose-6-phosphatase and other ChREBP target genes in hepatocytes [J].
Arden, Catherine ;
Tudhope, Susan J. ;
Petrie, John L. ;
Al-Oanzi, Ziad H. ;
Cullen, Kirsty S. ;
Lange, Alex J. ;
Towle, Howard C. ;
Agius, Loranne .
BIOCHEMICAL JOURNAL, 2012, 443 :111-123
[4]   The lipogenic transcription factor ChREBP dissociates hepatic steatosis from insulin resistance in mice and humans [J].
Benhamed, Fadila ;
Denechaud, Pierre-Damien ;
Lemoine, Maud ;
Robichon, Celine ;
Moldes, Marthe ;
Bertrand-Michel, Justine ;
Ratziu, Vlad ;
Serfaty, Lawrence ;
Housset, Chantal ;
Capeau, Jacqueline ;
Girard, Jean ;
Guillou, Herve ;
Postic, Catherine .
JOURNAL OF CLINICAL INVESTIGATION, 2012, 122 (06) :2176-2194
[5]   Gap junctions and other mechanisms of cell-cell communication regulate basal insulin secretion in the pancreatic islet [J].
Benninger, R. K. P. ;
Head, W. Steven ;
Zhang, Min ;
Satin, Leslie S. ;
Piston, David W. .
JOURNAL OF PHYSIOLOGY-LONDON, 2011, 589 (22) :5453-5466
[6]   Mix, a novel max-like BHLHZip protein that interacts with the max network of transcription factors [J].
Billin, AN ;
Eilers, AL ;
Queva, C ;
Ayer, DE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (51) :36344-36350
[7]   ChREBP Mediates Glucose Repression of Peroxisome Proliferator-activated Receptor α Expression in Pancreatic β-Cells [J].
Boergesen, Michael ;
Poulsen, Lars la Cour ;
Schmidt, Soren Fisker ;
Frigerio, Francesca ;
Maechler, Pierre ;
Mandrup, Susanne .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (15) :13214-13225
[8]   Salt-inducible kinase 2 links transcriptional coactivator p300 phosphorylation to the prevention of ChREBP-dependent hepatic steatosis in mice [J].
Bricambert, Julien ;
Miranda, Jonatan ;
Benhamed, Fadila ;
Postic, Jean Girard Catherine ;
Dentin, Renaud .
JOURNAL OF CLINICAL INVESTIGATION, 2010, 120 (12) :4316-4331
[9]   Absence of effects of Sir2 overexpression on lifespan in C. elegans and Drosophila [J].
Burnett, Camilla ;
Valentini, Sara ;
Cabreiro, Filipe ;
Goss, Martin ;
Somogyvari, Milan ;
Piper, Matthew D. ;
Hoddinott, Matthew ;
Sutphin, George L. ;
Leko, Vid ;
McElwee, Joshua J. ;
Vazquez-Manrique, Rafael P. ;
Orfila, Anne-Marie ;
Ackerman, Daniel ;
Au, Catherine ;
Vinti, Giovanna ;
Riesen, Michele ;
Howard, Ken ;
Neri, Christian ;
Bedalov, Antonio ;
Kaeberlein, Matt ;
Soti, Csaba ;
Partridge, Linda ;
Gems, David .
NATURE, 2011, 477 (7365) :482-U136
[10]   β-cell deficit and increased β-cell apoptosis in humans with type 2 diabetes [J].
Butler, AE ;
Janson, J ;
Bonner-Weir, S ;
Ritzel, R ;
Rizza, RA ;
Butler, PC .
DIABETES, 2003, 52 (01) :102-110