Novel insights into ChREBP regulation and function

被引:165
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
    Adams, A. C.
    Kharitonenkov, A.
    [J]. CURRENT DIABETES REVIEWS, 2012, 8 (04) : 285 - 293
  • [2] Glucose 6-phosphate regulates hepatic glycogenolysis through inactivation of phosphorylase
    Aiston, S
    Andersen, B
    Agius, L
    [J]. 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
    Arden, Catherine
    Tudhope, Susan J.
    Petrie, John L.
    Al-Oanzi, Ziad H.
    Cullen, Kirsty S.
    Lange, Alex J.
    Towle, Howard C.
    Agius, Loranne
    [J]. BIOCHEMICAL JOURNAL, 2012, 443 : 111 - 123
  • [4] The lipogenic transcription factor ChREBP dissociates hepatic steatosis from insulin resistance in mice and humans
    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
    [J]. 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
    Benninger, R. K. P.
    Head, W. Steven
    Zhang, Min
    Satin, Leslie S.
    Piston, David W.
    [J]. 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
    Billin, AN
    Eilers, AL
    Queva, C
    Ayer, DE
    [J]. 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
    Boergesen, Michael
    Poulsen, Lars la Cour
    Schmidt, Soren Fisker
    Frigerio, Francesca
    Maechler, Pierre
    Mandrup, Susanne
    [J]. 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
    Bricambert, Julien
    Miranda, Jonatan
    Benhamed, Fadila
    Postic, Jean Girard Catherine
    Dentin, Renaud
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2010, 120 (12) : 4316 - 4331
  • [9] Absence of effects of Sir2 overexpression on lifespan in C. elegans and Drosophila
    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
    [J]. NATURE, 2011, 477 (7365) : 482 - U136
  • [10] β-cell deficit and increased β-cell apoptosis in humans with type 2 diabetes
    Butler, AE
    Janson, J
    Bonner-Weir, S
    Ritzel, R
    Rizza, RA
    Butler, PC
    [J]. DIABETES, 2003, 52 (01) : 102 - 110