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Corrupted adipose tissue endogenous myelopoiesis initiates diet-induced metabolic disease
Activation and increased numbers of inflammatory macrophages, in adipose tissue (AT) are deleterious in metabolic diseases. Up to now, AT macrophages (ATM) accumulation was considered to be due to blood infiltration or local proliferation, although the presence of resident hematopoietic stem/progeni...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5509432/ https://www.ncbi.nlm.nih.gov/pubmed/28656887 http://dx.doi.org/10.7554/eLife.23194 |
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author | Luche, Elodie Robert, Virginie Cuminetti, Vincent Pomié, Celine Sastourné-Arrey, Quentin Waget, Aurélie Arnaud, Emmanuelle Varin, Audrey Labit, Elodie Laharrague, Patrick Burcelin, Remy Casteilla, Louis Cousin, Beatrice |
author_facet | Luche, Elodie Robert, Virginie Cuminetti, Vincent Pomié, Celine Sastourné-Arrey, Quentin Waget, Aurélie Arnaud, Emmanuelle Varin, Audrey Labit, Elodie Laharrague, Patrick Burcelin, Remy Casteilla, Louis Cousin, Beatrice |
author_sort | Luche, Elodie |
collection | PubMed |
description | Activation and increased numbers of inflammatory macrophages, in adipose tissue (AT) are deleterious in metabolic diseases. Up to now, AT macrophages (ATM) accumulation was considered to be due to blood infiltration or local proliferation, although the presence of resident hematopoietic stem/progenitor cells (Lin-/Sca+/c-Kit+; LSK phenotype) in the AT (AT-LSK) has been reported. By using transplantation of sorted AT-LSK and gain and loss of function studies we show that some of the inflammatory ATM inducing metabolic disease, originate from resident AT-LSK. Transplantation of AT-LSK sorted from high fat diet-fed (HFD) mice is sufficient to induce ATM accumulation, and to transfer metabolic disease in control mice. Conversely, the transplantation of control AT-LSK improves both AT-inflammation and glucose homeostasis in HFD mice. Our results clearly demonstrate that resident AT-LSK are one of the key point of metabolic disease, and could thus constitute a new promising therapeutic target to fight against metabolic disease. DOI: http://dx.doi.org/10.7554/eLife.23194.001 |
format | Online Article Text |
id | pubmed-5509432 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-55094322017-07-17 Corrupted adipose tissue endogenous myelopoiesis initiates diet-induced metabolic disease Luche, Elodie Robert, Virginie Cuminetti, Vincent Pomié, Celine Sastourné-Arrey, Quentin Waget, Aurélie Arnaud, Emmanuelle Varin, Audrey Labit, Elodie Laharrague, Patrick Burcelin, Remy Casteilla, Louis Cousin, Beatrice eLife Developmental Biology and Stem Cells Activation and increased numbers of inflammatory macrophages, in adipose tissue (AT) are deleterious in metabolic diseases. Up to now, AT macrophages (ATM) accumulation was considered to be due to blood infiltration or local proliferation, although the presence of resident hematopoietic stem/progenitor cells (Lin-/Sca+/c-Kit+; LSK phenotype) in the AT (AT-LSK) has been reported. By using transplantation of sorted AT-LSK and gain and loss of function studies we show that some of the inflammatory ATM inducing metabolic disease, originate from resident AT-LSK. Transplantation of AT-LSK sorted from high fat diet-fed (HFD) mice is sufficient to induce ATM accumulation, and to transfer metabolic disease in control mice. Conversely, the transplantation of control AT-LSK improves both AT-inflammation and glucose homeostasis in HFD mice. Our results clearly demonstrate that resident AT-LSK are one of the key point of metabolic disease, and could thus constitute a new promising therapeutic target to fight against metabolic disease. DOI: http://dx.doi.org/10.7554/eLife.23194.001 eLife Sciences Publications, Ltd 2017-06-28 /pmc/articles/PMC5509432/ /pubmed/28656887 http://dx.doi.org/10.7554/eLife.23194 Text en © 2017, Luche et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Developmental Biology and Stem Cells Luche, Elodie Robert, Virginie Cuminetti, Vincent Pomié, Celine Sastourné-Arrey, Quentin Waget, Aurélie Arnaud, Emmanuelle Varin, Audrey Labit, Elodie Laharrague, Patrick Burcelin, Remy Casteilla, Louis Cousin, Beatrice Corrupted adipose tissue endogenous myelopoiesis initiates diet-induced metabolic disease |
title | Corrupted adipose tissue endogenous myelopoiesis initiates diet-induced metabolic disease |
title_full | Corrupted adipose tissue endogenous myelopoiesis initiates diet-induced metabolic disease |
title_fullStr | Corrupted adipose tissue endogenous myelopoiesis initiates diet-induced metabolic disease |
title_full_unstemmed | Corrupted adipose tissue endogenous myelopoiesis initiates diet-induced metabolic disease |
title_short | Corrupted adipose tissue endogenous myelopoiesis initiates diet-induced metabolic disease |
title_sort | corrupted adipose tissue endogenous myelopoiesis initiates diet-induced metabolic disease |
topic | Developmental Biology and Stem Cells |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5509432/ https://www.ncbi.nlm.nih.gov/pubmed/28656887 http://dx.doi.org/10.7554/eLife.23194 |
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