FOXC2 is a winged helix gene that counteracts obesity, hypertriglyceridemia, and diet-induced insulin resistance

被引:542
作者
Cederberg, A
Gronning, LM
Ahrén, B
Taskén, K
Carlsson, P
Enerbäck, S
机构
[1] Univ Gothenburg, Dept Med Biochem, SE-40530 Gothenburg, Sweden
[2] Univ Oslo, Inst Med Biochem, N-0317 Oslo, Norway
[3] Lund Univ, Malmo Univ Hosp, Dept Med, SE-20520 Malmo, Sweden
关键词
D O I
10.1016/S0092-8674(01)00474-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Obesity, hyperlipidemia, and insulin resistance are common forerunners of type 2 diabetes mellitus. We have identified the human winged helix/forkhead transcription factor gene FOXC2 as a key regulator of adipocyte metabolism. Increased FOXC2 expression, in adipocytes, has a pleiotropic effect on gene expression, which leads to a lean and insulin sensitive phenotype. FOXC2 affects adipocyte metabolism by increasing the sensitivity of the beta -adrenergic-cAMP-protein kinase A (PIKA) signaling pathway through alteration of adipocyte PKA holoenzyme composition. Increased FOXC2 levels, induced by high fat diet, seem to counteract most of the symptoms associated with obesity, including hypertriglyceridemia and diet-induced insulin resistance-a likely consequence hereof would bo protection against type 2 diabetes.
引用
收藏
页码:563 / 573
页数:11
相关论文
共 43 条
[1]
COMPARISON OF BODY-COMPOSITION, ADIPOCYTE SIZE, AND GLUCOSE AND INSULIN CONCENTRATIONS IN PIMA INDIAN AND CAUCASIAN CHILDREN [J].
ABBOTT, WGH ;
FOLEY, JE .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1987, 36 (06) :576-579
[2]
Role of fatty acids in the pathogenesis of insulin resistance and NIDDM [J].
Boden, G .
DIABETES, 1997, 46 (01) :3-10
[3]
THE RESPONSE TO LONG-TERM OVERFEEDING IN IDENTICAL-TWINS [J].
BOUCHARD, C ;
TREMBLAY, A ;
DESPRES, JP ;
NADEAU, A ;
LUPIEN, PJ ;
THERIAULT, G ;
DUSSAULT, J ;
MOORJANI, S ;
PINAULT, S ;
FOURNIER, G .
NEW ENGLAND JOURNAL OF MEDICINE, 1990, 322 (21) :1477-1482
[4]
DIFFERENTIATION-INDUCED GENE-EXPRESSION IN 3T3-L1 PREADIPOCYTES - CCAAT ENHANCER BINDING-PROTEIN INTERACTS WITH AND ACTIVATES THE PROMOTERS OF 2 ADIPOCYTE-SPECIFIC GENES [J].
CHRISTY, RJ ;
YANG, VW ;
NTAMBI, JM ;
GEIMAN, DE ;
LANDSCHULZ, WH ;
FRIEDMAN, AD ;
NAKABEPPU, Y ;
KELLY, TJ ;
LANE, MD .
GENES & DEVELOPMENT, 1989, 3 (09) :1323-1335
[5]
Coe NR, 1999, J LIPID RES, V40, P967
[6]
Genetically lean mice result from targeted disruption of the RII beta subunit of protein kinase A [J].
Cummings, DE ;
Brandon, EP ;
Planas, JV ;
Motamed, K ;
Idzerda, RL ;
McKnight, GS .
NATURE, 1996, 382 (6592) :622-626
[7]
DOSTMANN WRG, 1990, J BIOL CHEM, V265, P10484
[8]
CHARACTERIZATION OF THE HUMAN LIPOPROTEIN-LIPASE (LPL) PROMOTER - EVIDENCE OF 2 CIS-REGULATORY REGIONS, LP-ALPHA AND LP-BETA, OF IMPORTANCE FOR THE DIFFERENTIATION-LINKED INDUCTION OF THE LPL GENE DURING ADIPOGENESIS [J].
ENERBACK, S ;
OHLSSON, BG ;
SAMUELSSON, L ;
BJURSELL, G .
MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (10) :4622-4633
[9]
Mice lacking mitochondrial uncoupling protein are cold-sensitive but not obese [J].
Enerback, S ;
Jacobsson, A ;
Simpson, EM ;
Guerra, C ;
Yamashita, H ;
Harper, ME ;
Kozak, LP .
NATURE, 1997, 387 (6628) :90-94
[10]
Fajas L, 1999, MOL CELL BIOL, V19, P5495