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T Cell Activation Inhibitors Reduce CD8+ T Cell and Pro-Inflammatory Macrophage Accumulation in Adipose Tissue of Obese Mice

Adipose tissue inflammation and specifically, pro-inflammatory macrophages are believed to contribute to insulin resistance (IR) in obesity in humans and animal models. Recent studies have invoked T cells in the recruitment of pro-inflammatory macrophages and the development of IR. To test the role...

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Autores principales: Montes, Vince N., Turner, Michael S., Subramanian, Savitha, Ding, Yilei, Hayden-Ledbetter, Martha, Slater, Sonya, Goodspeed, Leela, Wang, Shari, Omer, Mohamed, Den Hartigh, Laura J., Averill, Michelle M., O’Brien, Kevin D., Ledbetter, Jeffrey, Chait, Alan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3699637/
https://www.ncbi.nlm.nih.gov/pubmed/23844072
http://dx.doi.org/10.1371/journal.pone.0067709
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author Montes, Vince N.
Turner, Michael S.
Subramanian, Savitha
Ding, Yilei
Hayden-Ledbetter, Martha
Slater, Sonya
Goodspeed, Leela
Wang, Shari
Omer, Mohamed
Den Hartigh, Laura J.
Averill, Michelle M.
O’Brien, Kevin D.
Ledbetter, Jeffrey
Chait, Alan
author_facet Montes, Vince N.
Turner, Michael S.
Subramanian, Savitha
Ding, Yilei
Hayden-Ledbetter, Martha
Slater, Sonya
Goodspeed, Leela
Wang, Shari
Omer, Mohamed
Den Hartigh, Laura J.
Averill, Michelle M.
O’Brien, Kevin D.
Ledbetter, Jeffrey
Chait, Alan
author_sort Montes, Vince N.
collection PubMed
description Adipose tissue inflammation and specifically, pro-inflammatory macrophages are believed to contribute to insulin resistance (IR) in obesity in humans and animal models. Recent studies have invoked T cells in the recruitment of pro-inflammatory macrophages and the development of IR. To test the role of the T cell response in adipose tissue of mice fed an obesogenic diet, we used two agents (CTLA-4 Ig and anti-CD40L antibody) that block co-stimulation, which is essential for full T cell activation. C57BL/6 mice were fed an obesogenic diet for 16 weeks, and concomitantly either treated with CTLA-4 Ig, anti-CD40L antibody or an IgG control (300 µg/week). The treatments altered the immune cell composition of adipose tissue in obese mice. Treated mice demonstrated a marked reduction in pro-inflammatory adipose tissue macrophages and activated CD8+ T cells. Mice treated with anti-CD40L exhibited reduced weight gain, which was accompanied by a trend toward improved IR. CTLA-4 Ig treatment, however, was not associated with improved IR. These data suggest that the presence of pro-inflammatory T cells and macrophages can be altered with co-stimulatory inhibitors, but may not be a significant contributor to the whole body IR phenotype.
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spelling pubmed-36996372013-07-10 T Cell Activation Inhibitors Reduce CD8+ T Cell and Pro-Inflammatory Macrophage Accumulation in Adipose Tissue of Obese Mice Montes, Vince N. Turner, Michael S. Subramanian, Savitha Ding, Yilei Hayden-Ledbetter, Martha Slater, Sonya Goodspeed, Leela Wang, Shari Omer, Mohamed Den Hartigh, Laura J. Averill, Michelle M. O’Brien, Kevin D. Ledbetter, Jeffrey Chait, Alan PLoS One Research Article Adipose tissue inflammation and specifically, pro-inflammatory macrophages are believed to contribute to insulin resistance (IR) in obesity in humans and animal models. Recent studies have invoked T cells in the recruitment of pro-inflammatory macrophages and the development of IR. To test the role of the T cell response in adipose tissue of mice fed an obesogenic diet, we used two agents (CTLA-4 Ig and anti-CD40L antibody) that block co-stimulation, which is essential for full T cell activation. C57BL/6 mice were fed an obesogenic diet for 16 weeks, and concomitantly either treated with CTLA-4 Ig, anti-CD40L antibody or an IgG control (300 µg/week). The treatments altered the immune cell composition of adipose tissue in obese mice. Treated mice demonstrated a marked reduction in pro-inflammatory adipose tissue macrophages and activated CD8+ T cells. Mice treated with anti-CD40L exhibited reduced weight gain, which was accompanied by a trend toward improved IR. CTLA-4 Ig treatment, however, was not associated with improved IR. These data suggest that the presence of pro-inflammatory T cells and macrophages can be altered with co-stimulatory inhibitors, but may not be a significant contributor to the whole body IR phenotype. Public Library of Science 2013-07-02 /pmc/articles/PMC3699637/ /pubmed/23844072 http://dx.doi.org/10.1371/journal.pone.0067709 Text en © 2013 Montes et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Montes, Vince N.
Turner, Michael S.
Subramanian, Savitha
Ding, Yilei
Hayden-Ledbetter, Martha
Slater, Sonya
Goodspeed, Leela
Wang, Shari
Omer, Mohamed
Den Hartigh, Laura J.
Averill, Michelle M.
O’Brien, Kevin D.
Ledbetter, Jeffrey
Chait, Alan
T Cell Activation Inhibitors Reduce CD8+ T Cell and Pro-Inflammatory Macrophage Accumulation in Adipose Tissue of Obese Mice
title T Cell Activation Inhibitors Reduce CD8+ T Cell and Pro-Inflammatory Macrophage Accumulation in Adipose Tissue of Obese Mice
title_full T Cell Activation Inhibitors Reduce CD8+ T Cell and Pro-Inflammatory Macrophage Accumulation in Adipose Tissue of Obese Mice
title_fullStr T Cell Activation Inhibitors Reduce CD8+ T Cell and Pro-Inflammatory Macrophage Accumulation in Adipose Tissue of Obese Mice
title_full_unstemmed T Cell Activation Inhibitors Reduce CD8+ T Cell and Pro-Inflammatory Macrophage Accumulation in Adipose Tissue of Obese Mice
title_short T Cell Activation Inhibitors Reduce CD8+ T Cell and Pro-Inflammatory Macrophage Accumulation in Adipose Tissue of Obese Mice
title_sort t cell activation inhibitors reduce cd8+ t cell and pro-inflammatory macrophage accumulation in adipose tissue of obese mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3699637/
https://www.ncbi.nlm.nih.gov/pubmed/23844072
http://dx.doi.org/10.1371/journal.pone.0067709
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