Atf4 Regulates Obesity, Glucose Homeostasis, and Energy Expenditure

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OBJECTIVE-We evaluate a potential role of activating transcription factor 4 (Atf4) in invertebrate and mammalian metabolism. RESEARCH DESIGN AND METHODS-With two parallel approaches-a fat body-specific green fluorescent protein enhancer trap screen in D. melanogaster and expression profiling of developing murine fat tissues-we identified Atf4 as expressed in invertebrate and vertebrate metabolic tissues. We assessed the functional relevance of the evolutionarily conserved expression by analyzing Atf4 mutant flies and Atf4 mutant mice for possible metabolic phenotypes. RESULTS-Flies with insertions at the Atf4 locus have reduced fat content, increased starvation sensitivity, and lower levels of circulating carbohydrate. Atf4 null mice are also lean, and they resist age-related and diet-induced, obesity. Atf4 null mice have increased energy expenditure potentially accounting for the lean phenotype. Atf4 null mice are hypoglycemic, even before substantial changes in fat content, indicating that Atf4 regulates mammalian carbohydrate metabolism. In addition, the Atf4 mutation blunts diet-induced diabetes as well as hyperlipidemia and hepatosteatosis. Several aspects of the Atf4 mutant phenotype resemble mice with mutations in components of the target of rapamycin (TOR) pathway. Consistent with the phenotypic similarities, Atf4 null mice have reduced expression of genes that, regulate intracellular amino acid concentrations and lower intracellular concentration of amino acids, a key TOR input. Further, Atf4 mutants have reduced S6K activity in liver and adipose tissues. CONCLUSIONS-Atf4 regulates age-related and diet-induced obesity as well as glucose homeostasis in mammals and has conserved metabolic functions in flies. Diabetes 58:2565-2573, 2009
Publisher
AMER DIABETES ASSOC
Issue Date
2009-11
Language
English
Article Type
Article
Keywords

UNFOLDED PROTEIN RESPONSE; INSULIN-RESISTANCE; ENDOPLASMIC-RETICULUM; TRANSLATIONAL CONTROL; ADIPOSE-TISSUE; TARGETED DISRUPTION; OXIDATIVE STRESS; CELL-SURVIVAL; IN-VIVO; GENE

Citation

DIABETES, v.58, no.11, pp.2565 - 2573

ISSN
0012-1797
DOI
10.2337/db09-0335
URI
http://hdl.handle.net/10203/198274
Appears in Collection
MSE-Journal Papers(저널논문)
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