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BMPs as new insulin sensitizers: enhanced glucose uptake in mature 3T3-L1 adipocytes via PPARγ and GLUT4 upregulation

Insulin-resistance is the main cause of type 2 diabetes. Here we describe the identification and characterization of BMP2 and BMP6 as new insulin-sensitizing growth factors in mature adipocytes. We show that BMP2 and BMP6 lead to enhanced insulin-mediated glucose uptake in both insulin-sensitive and...

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Autores principales: Schreiber, Isabelle, Dörpholz, Gina, Ott, Claus-Eric, Kragesteen, Bjørt, Schanze, Nancy, Lee, Cory Thomas, Köhrle, Josef, Mundlos, Stefan, Ruschke, Karen, Knaus, Petra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5722815/
https://www.ncbi.nlm.nih.gov/pubmed/29222456
http://dx.doi.org/10.1038/s41598-017-17595-5
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author Schreiber, Isabelle
Dörpholz, Gina
Ott, Claus-Eric
Kragesteen, Bjørt
Schanze, Nancy
Lee, Cory Thomas
Köhrle, Josef
Mundlos, Stefan
Ruschke, Karen
Knaus, Petra
author_facet Schreiber, Isabelle
Dörpholz, Gina
Ott, Claus-Eric
Kragesteen, Bjørt
Schanze, Nancy
Lee, Cory Thomas
Köhrle, Josef
Mundlos, Stefan
Ruschke, Karen
Knaus, Petra
author_sort Schreiber, Isabelle
collection PubMed
description Insulin-resistance is the main cause of type 2 diabetes. Here we describe the identification and characterization of BMP2 and BMP6 as new insulin-sensitizing growth factors in mature adipocytes. We show that BMP2 and BMP6 lead to enhanced insulin-mediated glucose uptake in both insulin-sensitive and -insensitive adipocytes. We exclude a direct effect of BMP2 or BMP6 on translocation of GLUT4 to the plasma membrane and demonstrate that these BMPs increase GLUT4 protein levels equipotent to Rosiglitazone. BMPs induce expression of PPARγ as the crucial mediator for the insulin-sensitizing effect. A comprehensive RNA-Seq analysis in mature adipocytes revealed regulation of both BMP/Smad and PPARγ target genes. The effects of BMP2 and BMP6 are not completely redundant and include regulation of genes involved in glucose and fatty acid metabolism and adipokine expression. Collectively, these findings suggest the BMP2 and BMP6 pathway(s) as promising new drug targets to treat insulin resistance.
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spelling pubmed-57228152017-12-12 BMPs as new insulin sensitizers: enhanced glucose uptake in mature 3T3-L1 adipocytes via PPARγ and GLUT4 upregulation Schreiber, Isabelle Dörpholz, Gina Ott, Claus-Eric Kragesteen, Bjørt Schanze, Nancy Lee, Cory Thomas Köhrle, Josef Mundlos, Stefan Ruschke, Karen Knaus, Petra Sci Rep Article Insulin-resistance is the main cause of type 2 diabetes. Here we describe the identification and characterization of BMP2 and BMP6 as new insulin-sensitizing growth factors in mature adipocytes. We show that BMP2 and BMP6 lead to enhanced insulin-mediated glucose uptake in both insulin-sensitive and -insensitive adipocytes. We exclude a direct effect of BMP2 or BMP6 on translocation of GLUT4 to the plasma membrane and demonstrate that these BMPs increase GLUT4 protein levels equipotent to Rosiglitazone. BMPs induce expression of PPARγ as the crucial mediator for the insulin-sensitizing effect. A comprehensive RNA-Seq analysis in mature adipocytes revealed regulation of both BMP/Smad and PPARγ target genes. The effects of BMP2 and BMP6 are not completely redundant and include regulation of genes involved in glucose and fatty acid metabolism and adipokine expression. Collectively, these findings suggest the BMP2 and BMP6 pathway(s) as promising new drug targets to treat insulin resistance. Nature Publishing Group UK 2017-12-08 /pmc/articles/PMC5722815/ /pubmed/29222456 http://dx.doi.org/10.1038/s41598-017-17595-5 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Schreiber, Isabelle
Dörpholz, Gina
Ott, Claus-Eric
Kragesteen, Bjørt
Schanze, Nancy
Lee, Cory Thomas
Köhrle, Josef
Mundlos, Stefan
Ruschke, Karen
Knaus, Petra
BMPs as new insulin sensitizers: enhanced glucose uptake in mature 3T3-L1 adipocytes via PPARγ and GLUT4 upregulation
title BMPs as new insulin sensitizers: enhanced glucose uptake in mature 3T3-L1 adipocytes via PPARγ and GLUT4 upregulation
title_full BMPs as new insulin sensitizers: enhanced glucose uptake in mature 3T3-L1 adipocytes via PPARγ and GLUT4 upregulation
title_fullStr BMPs as new insulin sensitizers: enhanced glucose uptake in mature 3T3-L1 adipocytes via PPARγ and GLUT4 upregulation
title_full_unstemmed BMPs as new insulin sensitizers: enhanced glucose uptake in mature 3T3-L1 adipocytes via PPARγ and GLUT4 upregulation
title_short BMPs as new insulin sensitizers: enhanced glucose uptake in mature 3T3-L1 adipocytes via PPARγ and GLUT4 upregulation
title_sort bmps as new insulin sensitizers: enhanced glucose uptake in mature 3t3-l1 adipocytes via pparγ and glut4 upregulation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5722815/
https://www.ncbi.nlm.nih.gov/pubmed/29222456
http://dx.doi.org/10.1038/s41598-017-17595-5
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