Cargando…
Adipocytes Secrete Leukotrienes: Contribution to Obesity-Associated Inflammation and Insulin Resistance in Mice
Leukotrienes (LTs) are potent proinflammatory mediators, and many important aspects of innate and adaptive immune responses are regulated by LTs. Key members of the LT synthesis pathway are overexpressed in adipose tissue (AT) during obesity, resulting in increased LT levels in this tissue. We obser...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Diabetes Association
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3425405/ https://www.ncbi.nlm.nih.gov/pubmed/22688342 http://dx.doi.org/10.2337/db11-1455 |
_version_ | 1782241371077214208 |
---|---|
author | Mothe-Satney, Isabelle Filloux, Chantal Amghar, Hind Pons, Catherine Bourlier, Virginie Galitzky, Jean Grimaldi, Paul A. Féral, Chloé C. Bouloumié, Anne Van Obberghen, Emmanuel Neels, Jaap G. |
author_facet | Mothe-Satney, Isabelle Filloux, Chantal Amghar, Hind Pons, Catherine Bourlier, Virginie Galitzky, Jean Grimaldi, Paul A. Féral, Chloé C. Bouloumié, Anne Van Obberghen, Emmanuel Neels, Jaap G. |
author_sort | Mothe-Satney, Isabelle |
collection | PubMed |
description | Leukotrienes (LTs) are potent proinflammatory mediators, and many important aspects of innate and adaptive immune responses are regulated by LTs. Key members of the LT synthesis pathway are overexpressed in adipose tissue (AT) during obesity, resulting in increased LT levels in this tissue. We observed that several mouse adipocyte cell lines and primary adipocytes from mice and humans both can secrete large amounts of LTs. Furthermore, this production increases with a high-fat diet (HFD) and positively correlates with adipocyte size. LTs produced by adipocytes play an important role in attracting macrophages and T cells in in vitro chemotaxis assays. Mice that are deficient for the enzyme 5-lipoxygenase (5-LO), and therefore lack LTs, exhibit a decrease in HFD-induced AT macrophage and T-cell infiltration and are partially protected from HFD-induced insulin resistance. Similarly, treatment of HFD-fed wild-type mice with the 5-LO inhibitor Zileuton also results in a reduction of AT macrophages and T cells, accompanied by a decrease in insulin resistance. Together, these findings suggest that LTs represent a novel target in the prevention or treatment of obesity-associated inflammation and insulin resistance. |
format | Online Article Text |
id | pubmed-3425405 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | American Diabetes Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-34254052013-09-01 Adipocytes Secrete Leukotrienes: Contribution to Obesity-Associated Inflammation and Insulin Resistance in Mice Mothe-Satney, Isabelle Filloux, Chantal Amghar, Hind Pons, Catherine Bourlier, Virginie Galitzky, Jean Grimaldi, Paul A. Féral, Chloé C. Bouloumié, Anne Van Obberghen, Emmanuel Neels, Jaap G. Diabetes Obesity Studies Leukotrienes (LTs) are potent proinflammatory mediators, and many important aspects of innate and adaptive immune responses are regulated by LTs. Key members of the LT synthesis pathway are overexpressed in adipose tissue (AT) during obesity, resulting in increased LT levels in this tissue. We observed that several mouse adipocyte cell lines and primary adipocytes from mice and humans both can secrete large amounts of LTs. Furthermore, this production increases with a high-fat diet (HFD) and positively correlates with adipocyte size. LTs produced by adipocytes play an important role in attracting macrophages and T cells in in vitro chemotaxis assays. Mice that are deficient for the enzyme 5-lipoxygenase (5-LO), and therefore lack LTs, exhibit a decrease in HFD-induced AT macrophage and T-cell infiltration and are partially protected from HFD-induced insulin resistance. Similarly, treatment of HFD-fed wild-type mice with the 5-LO inhibitor Zileuton also results in a reduction of AT macrophages and T cells, accompanied by a decrease in insulin resistance. Together, these findings suggest that LTs represent a novel target in the prevention or treatment of obesity-associated inflammation and insulin resistance. American Diabetes Association 2012-09 2012-08-17 /pmc/articles/PMC3425405/ /pubmed/22688342 http://dx.doi.org/10.2337/db11-1455 Text en © 2012 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details. |
spellingShingle | Obesity Studies Mothe-Satney, Isabelle Filloux, Chantal Amghar, Hind Pons, Catherine Bourlier, Virginie Galitzky, Jean Grimaldi, Paul A. Féral, Chloé C. Bouloumié, Anne Van Obberghen, Emmanuel Neels, Jaap G. Adipocytes Secrete Leukotrienes: Contribution to Obesity-Associated Inflammation and Insulin Resistance in Mice |
title | Adipocytes Secrete Leukotrienes: Contribution to Obesity-Associated Inflammation and Insulin Resistance in Mice |
title_full | Adipocytes Secrete Leukotrienes: Contribution to Obesity-Associated Inflammation and Insulin Resistance in Mice |
title_fullStr | Adipocytes Secrete Leukotrienes: Contribution to Obesity-Associated Inflammation and Insulin Resistance in Mice |
title_full_unstemmed | Adipocytes Secrete Leukotrienes: Contribution to Obesity-Associated Inflammation and Insulin Resistance in Mice |
title_short | Adipocytes Secrete Leukotrienes: Contribution to Obesity-Associated Inflammation and Insulin Resistance in Mice |
title_sort | adipocytes secrete leukotrienes: contribution to obesity-associated inflammation and insulin resistance in mice |
topic | Obesity Studies |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3425405/ https://www.ncbi.nlm.nih.gov/pubmed/22688342 http://dx.doi.org/10.2337/db11-1455 |
work_keys_str_mv | AT mothesatneyisabelle adipocytessecreteleukotrienescontributiontoobesityassociatedinflammationandinsulinresistanceinmice AT fillouxchantal adipocytessecreteleukotrienescontributiontoobesityassociatedinflammationandinsulinresistanceinmice AT amgharhind adipocytessecreteleukotrienescontributiontoobesityassociatedinflammationandinsulinresistanceinmice AT ponscatherine adipocytessecreteleukotrienescontributiontoobesityassociatedinflammationandinsulinresistanceinmice AT bourliervirginie adipocytessecreteleukotrienescontributiontoobesityassociatedinflammationandinsulinresistanceinmice AT galitzkyjean adipocytessecreteleukotrienescontributiontoobesityassociatedinflammationandinsulinresistanceinmice AT grimaldipaula adipocytessecreteleukotrienescontributiontoobesityassociatedinflammationandinsulinresistanceinmice AT feralchloec adipocytessecreteleukotrienescontributiontoobesityassociatedinflammationandinsulinresistanceinmice AT bouloumieanne adipocytessecreteleukotrienescontributiontoobesityassociatedinflammationandinsulinresistanceinmice AT vanobberghenemmanuel adipocytessecreteleukotrienescontributiontoobesityassociatedinflammationandinsulinresistanceinmice AT neelsjaapg adipocytessecreteleukotrienescontributiontoobesityassociatedinflammationandinsulinresistanceinmice |