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

Summary: 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 adip...

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Main Authors: 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
Format: Article
Language:English
Published: Elsevier 2018-12-01
Series:Cell Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2211124718318503
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spelling doaj-23f24c5f8f9c4498af7deb99b8eddc752020-11-24T21:40:39ZengElsevierCell Reports2211-12472018-12-01251232833298.e6Loss of Transcriptional Repression by BCL6 Confers Insulin Sensitivity in the Setting of ObesityMadhavi D. Senagolage0Meredith A. Sommars1Krithika Ramachandran2Christopher R. Futtner3Yasuhiro Omura4Amanda L. Allred5Jianing Wang6Cynthia Yang7Daniele Procissi8Ronald M. Evans9Xianlin Han10Ilya R. Bederman11Grant D. Barish12Division of Endocrinology, Metabolism, and Molecular Medicine, Department of Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USADivision of Endocrinology, Metabolism, and Molecular Medicine, Department of Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USADivision of Endocrinology, Metabolism, and Molecular Medicine, Department of Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USADivision of Endocrinology, Metabolism, and Molecular Medicine, Department of Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USADivision of Endocrinology, Metabolism, and Molecular Medicine, Department of Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USADivision of Endocrinology, Metabolism, and Molecular Medicine, Department of Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USABarshop Institute for Longevity and Aging Studies, University of Texas Health Science Center at San Antonio, San Antonio, TX 78245, USACenter for Translational Imaging, Departments of Radiology and Biomedical Engineering, Northwestern University, Chicago, IL 60611, USACenter for Translational Imaging, Departments of Radiology and Biomedical Engineering, Northwestern University, Chicago, IL 60611, USAHoward Hughes Medical Institute, The Salk Institute for Biological Studies, La Jolla, CA 92037, USABarshop Institute for Longevity and Aging Studies, University of Texas Health Science Center at San Antonio, San Antonio, TX 78245, USADepartment of Pediatrics, Case Western Reserve University, Cleveland, OH 44106, USADivision of Endocrinology, Metabolism, and Molecular Medicine, Department of Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA; Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, IL 60611, USA; Corresponding authorSummary: 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. : Senagolage et al. identify BCL6 as a key regulator of body fat distribution. BCL6 directly represses fatty acid biosynthetic and growth genes in adipocytes. Mice constitutively lacking adipocyte Bcl6 exhibit expansion of their subcutaneous adipose tissue, enhanced insulin sensitivity, and protection from hepatic steatosis. Keywords: obesity, BCL6, BCL-6, repressor, adipocyte, hypertrophy, subcutaneous fat, insulin sensitivity, lipogenesis, adipose tissue, FAHFA, fatty acid esters of hydroxy fatty acids, PAHSA, adiponectin, ceramidehttp://www.sciencedirect.com/science/article/pii/S2211124718318503
collection DOAJ
language English
format Article
sources DOAJ
author 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
spellingShingle 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
Loss of Transcriptional Repression by BCL6 Confers Insulin Sensitivity in the Setting of Obesity
Cell Reports
author_facet 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
author_sort Madhavi D. Senagolage
title Loss of Transcriptional Repression by BCL6 Confers Insulin Sensitivity in the Setting of Obesity
title_short Loss of Transcriptional Repression by BCL6 Confers Insulin Sensitivity in the Setting of Obesity
title_full Loss of Transcriptional Repression by BCL6 Confers Insulin Sensitivity in the Setting of Obesity
title_fullStr Loss of Transcriptional Repression by BCL6 Confers Insulin Sensitivity in the Setting of Obesity
title_full_unstemmed Loss of Transcriptional Repression by BCL6 Confers Insulin Sensitivity in the Setting of Obesity
title_sort loss of transcriptional repression by bcl6 confers insulin sensitivity in the setting of obesity
publisher Elsevier
series Cell Reports
issn 2211-1247
publishDate 2018-12-01
description Summary: 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. : Senagolage et al. identify BCL6 as a key regulator of body fat distribution. BCL6 directly represses fatty acid biosynthetic and growth genes in adipocytes. Mice constitutively lacking adipocyte Bcl6 exhibit expansion of their subcutaneous adipose tissue, enhanced insulin sensitivity, and protection from hepatic steatosis. Keywords: obesity, BCL6, BCL-6, repressor, adipocyte, hypertrophy, subcutaneous fat, insulin sensitivity, lipogenesis, adipose tissue, FAHFA, fatty acid esters of hydroxy fatty acids, PAHSA, adiponectin, ceramide
url http://www.sciencedirect.com/science/article/pii/S2211124718318503
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