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Weight Loss Improves the Adipogenic Capacity of Human Preadipocytes and Modulates Their Secretory Profile
Calorie restriction–induced weight loss is accompanied by profound changes in adipose tissue characteristics. To determine the effect of weight loss on differentiation of preadipocytes and secretory capacity of in vitro differentiated adipocytes, we established cultures of these cells from paired su...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Diabetes Association
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3661637/ https://www.ncbi.nlm.nih.gov/pubmed/23378611 http://dx.doi.org/10.2337/db12-0986 |
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author | Rossmeislová, Lenka Mališová, Lucia Kračmerová, Jana Tencerová, Michaela Kováčová, Zuzana Koc, Michal Šiklová-Vítková, Michaela Viquerie, Nathalie Langin, Dominique Štich, Vladimír |
author_facet | Rossmeislová, Lenka Mališová, Lucia Kračmerová, Jana Tencerová, Michaela Kováčová, Zuzana Koc, Michal Šiklová-Vítková, Michaela Viquerie, Nathalie Langin, Dominique Štich, Vladimír |
author_sort | Rossmeislová, Lenka |
collection | PubMed |
description | Calorie restriction–induced weight loss is accompanied by profound changes in adipose tissue characteristics. To determine the effect of weight loss on differentiation of preadipocytes and secretory capacity of in vitro differentiated adipocytes, we established cultures of these cells from paired subcutaneous adipose tissue biopsies obtained before and at the end of weight-reducing dietary intervention (DI) in 23 obese women. Based on lipid accumulation and the expression of differentiation markers, in vitro adipogenesis increased after weight loss and it was accompanied by enhanced expression of genes involved in de novo lipogenesis. This effect of weight loss was not driven by changes of peroxisome proliferator–activated receptor γ sensitivity to rosiglitazone. Weight loss also enhanced the expression of adiponectin and leptin while reducing that of monocyte chemoattractant protein 1 and interleukin-8 by cultured adipocytes. Thus, the weight-reducing (DI) increased adipogenic capacity of preadipocytes and shifted their secretion toward lower inflammatory profile. Reprogramming of preadipocytes could represent an adaptation to weight loss leading to partial restoration of preobese adipose tissue traits and thus contribute to the improvement of metabolic status. However, enhanced adipogenesis could also contribute to the unwanted weight regain after initial weight loss. |
format | Online Article Text |
id | pubmed-3661637 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | American Diabetes Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-36616372014-06-01 Weight Loss Improves the Adipogenic Capacity of Human Preadipocytes and Modulates Their Secretory Profile Rossmeislová, Lenka Mališová, Lucia Kračmerová, Jana Tencerová, Michaela Kováčová, Zuzana Koc, Michal Šiklová-Vítková, Michaela Viquerie, Nathalie Langin, Dominique Štich, Vladimír Diabetes Original Research Calorie restriction–induced weight loss is accompanied by profound changes in adipose tissue characteristics. To determine the effect of weight loss on differentiation of preadipocytes and secretory capacity of in vitro differentiated adipocytes, we established cultures of these cells from paired subcutaneous adipose tissue biopsies obtained before and at the end of weight-reducing dietary intervention (DI) in 23 obese women. Based on lipid accumulation and the expression of differentiation markers, in vitro adipogenesis increased after weight loss and it was accompanied by enhanced expression of genes involved in de novo lipogenesis. This effect of weight loss was not driven by changes of peroxisome proliferator–activated receptor γ sensitivity to rosiglitazone. Weight loss also enhanced the expression of adiponectin and leptin while reducing that of monocyte chemoattractant protein 1 and interleukin-8 by cultured adipocytes. Thus, the weight-reducing (DI) increased adipogenic capacity of preadipocytes and shifted their secretion toward lower inflammatory profile. Reprogramming of preadipocytes could represent an adaptation to weight loss leading to partial restoration of preobese adipose tissue traits and thus contribute to the improvement of metabolic status. However, enhanced adipogenesis could also contribute to the unwanted weight regain after initial weight loss. American Diabetes Association 2013-06 2013-05-17 /pmc/articles/PMC3661637/ /pubmed/23378611 http://dx.doi.org/10.2337/db12-0986 Text en © 2013 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 | Original Research Rossmeislová, Lenka Mališová, Lucia Kračmerová, Jana Tencerová, Michaela Kováčová, Zuzana Koc, Michal Šiklová-Vítková, Michaela Viquerie, Nathalie Langin, Dominique Štich, Vladimír Weight Loss Improves the Adipogenic Capacity of Human Preadipocytes and Modulates Their Secretory Profile |
title | Weight Loss Improves the Adipogenic Capacity of Human Preadipocytes and Modulates Their Secretory Profile |
title_full | Weight Loss Improves the Adipogenic Capacity of Human Preadipocytes and Modulates Their Secretory Profile |
title_fullStr | Weight Loss Improves the Adipogenic Capacity of Human Preadipocytes and Modulates Their Secretory Profile |
title_full_unstemmed | Weight Loss Improves the Adipogenic Capacity of Human Preadipocytes and Modulates Their Secretory Profile |
title_short | Weight Loss Improves the Adipogenic Capacity of Human Preadipocytes and Modulates Their Secretory Profile |
title_sort | weight loss improves the adipogenic capacity of human preadipocytes and modulates their secretory profile |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3661637/ https://www.ncbi.nlm.nih.gov/pubmed/23378611 http://dx.doi.org/10.2337/db12-0986 |
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