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Series GSE60527 Query DataSets for GSE60527
Status Public on Aug 20, 2014
Title Integrated Control of Hepatic Lipogenesis vs. Glucose Production Requires FoxO Transcription Factors
Organism Mus musculus
Experiment type Expression profiling by array
Summary Insulin integrates hepatic glucose and lipid metabolism, directing nutrients to storage as glycogen and triglyceride. In type 2 diabetes, levels of the former are low and the latter are exaggerated, posing a pathophysiologic and therapeutic conundrum. A branching model1 of insulin signaling, with FoxO1 presiding over glucose production2-5 and Srebp–1c regulating lipogenesis,6-8 provides a potential explanation. Here we illustrate an alternative mechanism that integrates glucose production and lipogenesis under the unifying control of FoxO. Liver–specific ablation of three FoxOs (L–FoxO1,3,4) prevents the induction of glucose–6–phosphatase and the repression of glucokinase during fasting, thus increasing lipogenesis at the expense of glucose production. We document a similar pattern in the early phases of diet-induced insulin resistance, and propose that FoxOs are required to enable the liver to direct nutritionally derived carbons to glucose vs. lipid metabolism. Our data underscore the heterogeneity of hepatic insulin resistance during progression from the metabolic syndrome to overt diabetes, and the conceptual challenge of designing therapies that curtail glucose production without promoting hepatic lipid accumulation.
We used microarrays to detail the change of gene expression in liver after knocking out FoxO1,3 and 4.
 
Overall design Liver tissue samples were collected from hepatocyte- specific triple FoxO(1,3, and 4) KO and their littermates control (WT) mice after fasting (22 h) or refeeding (4 h). Gene expression was analyzed by microarray. Mice were on a mixed background of C57BL/6J and 129.
 
Contributor(s) Accili D, Haeusler RA
Citation(s) 25307742
Submission date Aug 19, 2014
Last update date Mar 06, 2018
Contact name Rebecca Haeusler
E-mail(s) rah2130@columbia.edu
Organization name Columbia University
Department Pathology and Cell Biology
Street address 1150 Saint Nicholas Ave Room 303A
City New York
State/province NY
ZIP/Postal code 10032
Country USA
 
Platforms (1)
GPL6096 [MoEx-1_0-st] Affymetrix Mouse Exon 1.0 ST Array [transcript (gene) version]
Samples (12)
GSM1481689 C344
GSM1481690 C345
GSM1481691 C391
Relations
BioProject PRJNA258469

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE60527_RAW.tar 274.7 Mb (http)(custom) TAR (of CEL, CHP)
Processed data included within Sample table
Processed data provided as supplementary file

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