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Norway

PMID:30566857  

Loss of Transcriptional Repression by BCL6 Confers Insulin Sensitivity in the Setting of Obesity.

Madhavi D Senagolage | Meredith A Sommars | Krithika Ramachandran | Christopher R Futtner | Yasuhiro Omura | Amanda L Allred | Jianing Wang | Cynthia Yang | Daniele Procissi | Ronald M Evans | Xianlin Han | Ilya R Bederman | Grant D Barish
Cell reports | 2018

Accumulation of visceral adiposity is directly linked to the morbidity of obesity, while subcutaneous body fat is considered more benign. We have identified an unexpected role for B cell lymphoma 6 (BCL6), a critical regulator of immunity, in the developmental expansion of subcutaneous adipose tissue. In adipocyte-specific knockout mice (Bcl6AKO), we found that Bcl6 deletion results in strikingly increased inguinal, but not perigonadal, adipocyte size and tissue mass in addition to marked insulin sensitivity. Genome-wide RNA expression and DNA binding analyses revealed that BCL6 controls gene networks involved in cell growth and fatty acid biosynthesis. Using deuterium label incorporation and comprehensive adipokine and lipid profiling, we discovered that ablation of adipocyte Bcl6 enhances subcutaneous adipocyte lipogenesis, increases levels of adiponectin and fatty acid esters of hydroxy fatty acids (FAHFAs), and prevents steatosis. Thus, our studies identify BCL6 as a negative regulator of subcutaneous adipose tissue expansion and metabolic health.

Pubmed ID: 30566857

Associated grants

  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL105278
  • Agency: NHLBI NIH HHS, United States
    Id: K08 HL092298
  • Agency: NCI NIH HHS, United States
    Id: P30 CA060553
  • Agency: NIDDK NIH HHS, United States
    Id: R01 DK108987
  • Agency: NIDDK NIH HHS, United States
    Id: R37 DK057978
  • Agency: NIDDK NIH HHS, United States
    Id: P30 DK020595
  • Agency: NCI NIH HHS, United States
    Id: P30 CA014195

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This is a list of tools and resources that we have found mentioned in this publication.


ChIP-seq (tool)

RRID:SCR_001237

Set of software modules for performing common ChIP-seq data analysis tasks across the whole genome, including positional correlation analysis, peak detection, and genome partitioning into signal-rich and signal-poor regions. The tools are designed to be simple, fast and highly modular. Each program carries out a well defined data processing procedure that can potentially fit into a pipeline framework. ChIP-Seq is also freely available on a Web interface.

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RRID:SCR_002798

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Binding and Expression Target Analysis (tool)

RRID:SCR_005396

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RRID:SCR_016620

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RRID:IMSR_JAX:000664

Mus musculus with name C57BL/6J from IMSR.

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RRID:AB_11178660

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RRID:AB_2063455

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