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COUP-TFII controls mouse pancreatic ?-cell mass through GLP-1-?-catenin signaling pathways.

ABSTRACT: BACKGROUND:The control of the functional pancreatic ?-cell mass serves the key homeostatic function of releasing the right amount of insulin to keep blood sugar in the normal range. It is not fully understood though how ?-cell mass is determined. METHODOLOGY/PRINCIPAL FINDINGS:Conditional chicken ovalbumin upstream promoter transcription factor II (COUP-TFII)-deficient mice were generated and crossed with mice expressing Cre under the control of pancreatic duodenal homeobox 1 (pdx1) gene promoter. Ablation of COUP-TFII in pancreas resulted in glucose intolerance. Beta-cell number was reduced at 1 day and 3 weeks postnatal. Together with a reduced number of insulin-containing cells in the ductal epithelium and normal ?-cell proliferation and apoptosis, this suggests decreased ?-cell differentiation in the neonatal period. By testing islets isolated from these mice and cultured ?-cells with loss and gain of COUP-TFII function, we found that COUP-TFII induces the expression of the ?-catenin gene and its target genes such as cyclin D1 and axin 2. Moreover, induction of these genes by glucagon-like peptide 1 (GLP-1) via ?-catenin was impaired in absence of COUP-TFII. The expression of two other target genes of GLP-1 signaling, GLP-1R and PDX-1 was significantly lower in mutant islets compared to control islets, possibly contributing to reduced ?-cell mass. Finally, we demonstrated that COUP-TFII expression was activated by the Wnt signaling-associated transcription factor TCF7L2 (T-cell factor 7-like 2) in human islets and rat ?-cells providing a feedback loop. CONCLUSIONS/SIGNIFICANCE:Our findings show that COUP-TFII is a novel component of the GLP-1 signaling cascade that increases ?-cell number during the neonatal period. COUP-TFII is required for GLP-1 activation of the ?-catenin-dependent pathway and its expression is under the control of TCF7L2.

SUBMITTER: Boutant M

PROVIDER: S-EPMC3265526 | biostudies-literature | 2012

REPOSITORIES: biostudies-literature

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COUP-TFII controls mouse pancreatic β-cell mass through GLP-1-β-catenin signaling pathways.

Boutant Marie M Ramos Oscar Henrique Pereira OH Tourrel-Cuzin Cécile C Movassat Jamileh J Ilias Anissa A Vallois David D Planchais Julien J Pégorier Jean-Paul JP Schuit Frans F Petit Patrice X PX Bossard Pascale P Maedler Kathrin K Grapin-Botton Anne A Vasseur-Cognet Mireille M

PloS one 20120124 1

<h4>Background</h4>The control of the functional pancreatic β-cell mass serves the key homeostatic function of releasing the right amount of insulin to keep blood sugar in the normal range. It is not fully understood though how β-cell mass is determined.<h4>Methodology/principal findings</h4>Conditional chicken ovalbumin upstream promoter transcription factor II (COUP-TFII)-deficient mice were generated and crossed with mice expressing Cre under the control of pancreatic duodenal homeobox 1 (pdx ...[more]

PMID: 22292058

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Project description:Pancreatic β-cells have the key homeostatic function of releasing insulin to keep blood glucose in the normal range. It is not fully understood how β-cell mass is determined. Ablation of a nuclear receptor, chicken ovalbumin upstream promoter transcription factor II (COUP-TFII), in mouse pancreatic β-cells results in glucose intolerance and 50% fewer β-cells during the postnatal period. By testing islets isolated from these mice and cultured β-cells with loss and gain of COUP-TFII function, we found that COUP-TFII induces β-catenin thus upregulating target genes like cyclin D1. Beta-cell expansion triggered by glucagon-like peptide 1 (GLP-1) is known to be mediated by β-catenin controlling cyclin D1. We show that in the absence of COUP-TFII, exendin-4, an agonist of the GLP-1 receptor, does not fully induce cyclin D1 expression, while overexpression of β-catenin induces cyclin D1. A marked decrease in cyclin D1 expression is detected in islets isolated from transgenic mice lacking both GLP-1 receptor and gastric inhibitory peptide receptor. COUP-TFII is therefore required for GLP-1 activation of the β-catenin-dependent pathway in pancreatic β-cells to increase β-cell number. To understand the molecular mechanisms by which COUP-TFII controls β-cell mass, we determined the RNA profile of COUP-TFII knockdown β-cells using Affymetrix oligonucleotide microarrays. Computational analysis identified clusters of genes shared by different gene regulatory Networks that are up or down regulated namely genes involved in Wnt/β-catenin signaling, insulin signaling and lipid/carbohydrate metabolism. We determined the RNA profile of COUP-TFII knockdown β-cells (832/13 INS-1 cells transfected with COUP-TFII specific siRNA) with respect to control cells (832/13 INS-1 cells transfected with scrambled siRNA) using Affymetrix expression analysis technical manual 701025Rev.5 (Affymetrix, Santa Clara, California, USA). Briefly, 1 mg of total cellular mRNA was reverse transcribed into cDNA (SuperScript Choice System Invitrogen, Carlsbad, CA) using oligo-dT primers and a T7 RNA polymerase promoter site. The cDNA was in vitro transcribed and biotin-labeled for microarray analysis using the Affymetrix IVT labeling kit. The concentration of labelled cRNA was measured using a NanoDrop ND-1000 spectrophotometer. Labeled cRNA was fragmented in a fragmentation buffer for 35 min at 94°C. The quality of labeled and fragmented cRNA was analyzed using the Agilent bioanalyzer 2100 (Van Lommel et al, 2006). Fragmented cRNA was hybridized to the rat 230 2.0 array (Affymetrix) during 16h at 45°C. Arrays were washed and stained in a fluidics station (Affymetrix) and scanned using the Affymetrix 3000 GeneScanner.

Dataset Information

COUP-TFII controls mouse pancreatic ?-cell mass through GLP-1-?-catenin signaling pathways.

Publications

COUP-TFII controls mouse pancreatic β-cell mass through GLP-1-β-catenin signaling pathways.

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