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Fat Grafting Can Induce Browning of White Adipose Tissue
BACKGROUND: Fat grafting is commonly used when treating soft-tissue defects. However, much of the basic biology behind fat transfer is still uncovered. Adipocytes can be divided into energy storing white and energy burning brown adipose cells. It is now well known, that also adult humans have metabo...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6157953/ https://www.ncbi.nlm.nih.gov/pubmed/30276049 http://dx.doi.org/10.1097/GOX.0000000000001804 |
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author | Hoppela, Erika Grönroos, Tove J. Saarikko, Anne M. Tervala, Tomi V. Kauhanen, Susanna Nuutila, Pirjo Kivinen, Katri Hartiala, Pauliina |
author_facet | Hoppela, Erika Grönroos, Tove J. Saarikko, Anne M. Tervala, Tomi V. Kauhanen, Susanna Nuutila, Pirjo Kivinen, Katri Hartiala, Pauliina |
author_sort | Hoppela, Erika |
collection | PubMed |
description | BACKGROUND: Fat grafting is commonly used when treating soft-tissue defects. However, much of the basic biology behind fat transfer is still uncovered. Adipocytes can be divided into energy storing white and energy burning brown adipose cells. It is now well known, that also adult humans have metabolically active brown adipose tissue (BAT) within white adipose tissue (WAT). Previously our group showed that transfer of metabolically inactive WAT into a new environment increased the metabolic activity of the fat grafts to resemble the activity in the recipient site and that different WAT depots have variation in the metabolic activity. This led us to speculate, whether the metabolic increase of the graft is a result of “browning” of the transferred WAT toward beige adipose tissue. METHODS: We investigated the metabolic and histological characteristics and BAT marker Ucp1 gene expression in different types of WAT grafts placed either in subcutaneous or muscle tissue in mice. Metabolic activity of the grafts was investigated by FDG-PET/CT at 4- and 12-week time-points. RESULTS: The glucose uptake of all transferred fat types was increased when compared with respective control WAT regardless of transfer location. Ucp1 gene and protein expression was increased in 4 of 15 intramuscularly placed fat graft samples and showed histological resemblance to BAT with multilocular cells. CONCLUSIONS: Grafting of metabolically inactive fat intramuscularly may induce browning of fat grafts toward more active beige adipose tissue. This opens up new research areas in exploiting fat grafting in metabolic diseases. |
format | Online Article Text |
id | pubmed-6157953 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-61579532018-10-01 Fat Grafting Can Induce Browning of White Adipose Tissue Hoppela, Erika Grönroos, Tove J. Saarikko, Anne M. Tervala, Tomi V. Kauhanen, Susanna Nuutila, Pirjo Kivinen, Katri Hartiala, Pauliina Plast Reconstr Surg Glob Open Experimental BACKGROUND: Fat grafting is commonly used when treating soft-tissue defects. However, much of the basic biology behind fat transfer is still uncovered. Adipocytes can be divided into energy storing white and energy burning brown adipose cells. It is now well known, that also adult humans have metabolically active brown adipose tissue (BAT) within white adipose tissue (WAT). Previously our group showed that transfer of metabolically inactive WAT into a new environment increased the metabolic activity of the fat grafts to resemble the activity in the recipient site and that different WAT depots have variation in the metabolic activity. This led us to speculate, whether the metabolic increase of the graft is a result of “browning” of the transferred WAT toward beige adipose tissue. METHODS: We investigated the metabolic and histological characteristics and BAT marker Ucp1 gene expression in different types of WAT grafts placed either in subcutaneous or muscle tissue in mice. Metabolic activity of the grafts was investigated by FDG-PET/CT at 4- and 12-week time-points. RESULTS: The glucose uptake of all transferred fat types was increased when compared with respective control WAT regardless of transfer location. Ucp1 gene and protein expression was increased in 4 of 15 intramuscularly placed fat graft samples and showed histological resemblance to BAT with multilocular cells. CONCLUSIONS: Grafting of metabolically inactive fat intramuscularly may induce browning of fat grafts toward more active beige adipose tissue. This opens up new research areas in exploiting fat grafting in metabolic diseases. Wolters Kluwer Health 2018-06-19 /pmc/articles/PMC6157953/ /pubmed/30276049 http://dx.doi.org/10.1097/GOX.0000000000001804 Text en Copyright © 2018 The Authors. Published by Wolters Kluwer Health, Inc. on behalf of The American Society of Plastic Surgeons. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Experimental Hoppela, Erika Grönroos, Tove J. Saarikko, Anne M. Tervala, Tomi V. Kauhanen, Susanna Nuutila, Pirjo Kivinen, Katri Hartiala, Pauliina Fat Grafting Can Induce Browning of White Adipose Tissue |
title | Fat Grafting Can Induce Browning of White Adipose Tissue |
title_full | Fat Grafting Can Induce Browning of White Adipose Tissue |
title_fullStr | Fat Grafting Can Induce Browning of White Adipose Tissue |
title_full_unstemmed | Fat Grafting Can Induce Browning of White Adipose Tissue |
title_short | Fat Grafting Can Induce Browning of White Adipose Tissue |
title_sort | fat grafting can induce browning of white adipose tissue |
topic | Experimental |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6157953/ https://www.ncbi.nlm.nih.gov/pubmed/30276049 http://dx.doi.org/10.1097/GOX.0000000000001804 |
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