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A Renewable Source of Human Beige Adipocytes for Development of Therapies to Treat Metabolic Syndrome
Molecular- and cellular-based therapies have the potential to reduce obesity-associated disease. In response to cold, beige adipocytes form in subcutaneous white adipose tissue and convert energy stored in metabolic substrates to heat, making them an attractive therapeutic target. We developed a rob...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6375695/ https://www.ncbi.nlm.nih.gov/pubmed/30540952 http://dx.doi.org/10.1016/j.celrep.2018.11.037 |
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author | Su, Su Guntur, Anyonya R. Nguyen, Daniel C. Fakory, Shameem S. Doucette, Chad C. Leech, Cassandra Lotana, Humphrey Kelley, Matthew Kohli, Jaspreet Martino, Julieta Sims-Lucas, Sunder Liaw, Lucy Vary, Calvin Rosen, Clifford J. Brown, Aaron C. |
author_facet | Su, Su Guntur, Anyonya R. Nguyen, Daniel C. Fakory, Shameem S. Doucette, Chad C. Leech, Cassandra Lotana, Humphrey Kelley, Matthew Kohli, Jaspreet Martino, Julieta Sims-Lucas, Sunder Liaw, Lucy Vary, Calvin Rosen, Clifford J. Brown, Aaron C. |
author_sort | Su, Su |
collection | PubMed |
description | Molecular- and cellular-based therapies have the potential to reduce obesity-associated disease. In response to cold, beige adipocytes form in subcutaneous white adipose tissue and convert energy stored in metabolic substrates to heat, making them an attractive therapeutic target. We developed a robust method to generate a renewable source of human beige adipocytes from induced pluripotent stem cells (iPSCs). Developmentally, these cells are derived from FOXF1(+) mesoderm and progress through an expandable mural-like mesenchymal stem cell (MSC) to form mature beige adipocytes that display a thermogenically active profile. This includes expression of uncoupling protein 1 (UCP1) concomitant with increased uncoupled respiration. With this method, dysfunctional adipogenic precursors can be reprogrammed and differentiated into beige adipocytes with increased thermogenic function and anti-diabetic secretion potential. This resource can be used to (1) elucidate mechanisms that underlie the control of beige adipogenesis and (2) generate material for cellular-based therapies that target metabolic syndrome in humans. |
format | Online Article Text |
id | pubmed-6375695 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
record_format | MEDLINE/PubMed |
spelling | pubmed-63756952019-02-14 A Renewable Source of Human Beige Adipocytes for Development of Therapies to Treat Metabolic Syndrome Su, Su Guntur, Anyonya R. Nguyen, Daniel C. Fakory, Shameem S. Doucette, Chad C. Leech, Cassandra Lotana, Humphrey Kelley, Matthew Kohli, Jaspreet Martino, Julieta Sims-Lucas, Sunder Liaw, Lucy Vary, Calvin Rosen, Clifford J. Brown, Aaron C. Cell Rep Article Molecular- and cellular-based therapies have the potential to reduce obesity-associated disease. In response to cold, beige adipocytes form in subcutaneous white adipose tissue and convert energy stored in metabolic substrates to heat, making them an attractive therapeutic target. We developed a robust method to generate a renewable source of human beige adipocytes from induced pluripotent stem cells (iPSCs). Developmentally, these cells are derived from FOXF1(+) mesoderm and progress through an expandable mural-like mesenchymal stem cell (MSC) to form mature beige adipocytes that display a thermogenically active profile. This includes expression of uncoupling protein 1 (UCP1) concomitant with increased uncoupled respiration. With this method, dysfunctional adipogenic precursors can be reprogrammed and differentiated into beige adipocytes with increased thermogenic function and anti-diabetic secretion potential. This resource can be used to (1) elucidate mechanisms that underlie the control of beige adipogenesis and (2) generate material for cellular-based therapies that target metabolic syndrome in humans. 2018-12-11 /pmc/articles/PMC6375695/ /pubmed/30540952 http://dx.doi.org/10.1016/j.celrep.2018.11.037 Text en This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Su, Su Guntur, Anyonya R. Nguyen, Daniel C. Fakory, Shameem S. Doucette, Chad C. Leech, Cassandra Lotana, Humphrey Kelley, Matthew Kohli, Jaspreet Martino, Julieta Sims-Lucas, Sunder Liaw, Lucy Vary, Calvin Rosen, Clifford J. Brown, Aaron C. A Renewable Source of Human Beige Adipocytes for Development of Therapies to Treat Metabolic Syndrome |
title | A Renewable Source of Human Beige Adipocytes for Development of Therapies to Treat Metabolic Syndrome |
title_full | A Renewable Source of Human Beige Adipocytes for Development of Therapies to Treat Metabolic Syndrome |
title_fullStr | A Renewable Source of Human Beige Adipocytes for Development of Therapies to Treat Metabolic Syndrome |
title_full_unstemmed | A Renewable Source of Human Beige Adipocytes for Development of Therapies to Treat Metabolic Syndrome |
title_short | A Renewable Source of Human Beige Adipocytes for Development of Therapies to Treat Metabolic Syndrome |
title_sort | renewable source of human beige adipocytes for development of therapies to treat metabolic syndrome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6375695/ https://www.ncbi.nlm.nih.gov/pubmed/30540952 http://dx.doi.org/10.1016/j.celrep.2018.11.037 |
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