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Proteomic Analysis of Human Brown Adipose Tissue Reveals Utilization of Coupled and Uncoupled Energy Expenditure Pathways
Human brown adipose tissue (BAT) has become an attractive target to combat the current epidemical spread of obesity and its associated co-morbidities. Currently, information on its functional role is primarily derived from rodent studies. Here, we present the first comparative proteotype analysis of...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4945940/ https://www.ncbi.nlm.nih.gov/pubmed/27418403 http://dx.doi.org/10.1038/srep30030 |
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author | Müller, Sebastian Balaz, Miroslav Stefanicka, Patrik Varga, Lukas Amri, Ez-Zoubir Ukropec, Jozef Wollscheid, Bernd Wolfrum, Christian |
author_facet | Müller, Sebastian Balaz, Miroslav Stefanicka, Patrik Varga, Lukas Amri, Ez-Zoubir Ukropec, Jozef Wollscheid, Bernd Wolfrum, Christian |
author_sort | Müller, Sebastian |
collection | PubMed |
description | Human brown adipose tissue (BAT) has become an attractive target to combat the current epidemical spread of obesity and its associated co-morbidities. Currently, information on its functional role is primarily derived from rodent studies. Here, we present the first comparative proteotype analysis of primary human brown adipose tissue versus adjacent white adipose tissue, which reveals significant quantitative differences in protein abundances and in turn differential functional capabilities. The majority of the 318 proteins with increased abundance in BAT are associated with mitochondrial metabolism and confirm the increased oxidative capacity. In addition to uncoupling protein 1 (UCP1), the main functional effector for uncoupled respiration, we also detected the mitochondrial creatine kinases (CKMT1A/B, CKMT2), as effective modulators of ATP synthase coupled respiration, to be exclusively expressed in BAT. The abundant expression and utilization of both energy expenditure pathways in parallel highlights the complex functional involvement of BAT in human physiology. |
format | Online Article Text |
id | pubmed-4945940 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49459402016-07-26 Proteomic Analysis of Human Brown Adipose Tissue Reveals Utilization of Coupled and Uncoupled Energy Expenditure Pathways Müller, Sebastian Balaz, Miroslav Stefanicka, Patrik Varga, Lukas Amri, Ez-Zoubir Ukropec, Jozef Wollscheid, Bernd Wolfrum, Christian Sci Rep Article Human brown adipose tissue (BAT) has become an attractive target to combat the current epidemical spread of obesity and its associated co-morbidities. Currently, information on its functional role is primarily derived from rodent studies. Here, we present the first comparative proteotype analysis of primary human brown adipose tissue versus adjacent white adipose tissue, which reveals significant quantitative differences in protein abundances and in turn differential functional capabilities. The majority of the 318 proteins with increased abundance in BAT are associated with mitochondrial metabolism and confirm the increased oxidative capacity. In addition to uncoupling protein 1 (UCP1), the main functional effector for uncoupled respiration, we also detected the mitochondrial creatine kinases (CKMT1A/B, CKMT2), as effective modulators of ATP synthase coupled respiration, to be exclusively expressed in BAT. The abundant expression and utilization of both energy expenditure pathways in parallel highlights the complex functional involvement of BAT in human physiology. Nature Publishing Group 2016-07-15 /pmc/articles/PMC4945940/ /pubmed/27418403 http://dx.doi.org/10.1038/srep30030 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Müller, Sebastian Balaz, Miroslav Stefanicka, Patrik Varga, Lukas Amri, Ez-Zoubir Ukropec, Jozef Wollscheid, Bernd Wolfrum, Christian Proteomic Analysis of Human Brown Adipose Tissue Reveals Utilization of Coupled and Uncoupled Energy Expenditure Pathways |
title | Proteomic Analysis of Human Brown Adipose Tissue Reveals Utilization of Coupled and Uncoupled Energy Expenditure Pathways |
title_full | Proteomic Analysis of Human Brown Adipose Tissue Reveals Utilization of Coupled and Uncoupled Energy Expenditure Pathways |
title_fullStr | Proteomic Analysis of Human Brown Adipose Tissue Reveals Utilization of Coupled and Uncoupled Energy Expenditure Pathways |
title_full_unstemmed | Proteomic Analysis of Human Brown Adipose Tissue Reveals Utilization of Coupled and Uncoupled Energy Expenditure Pathways |
title_short | Proteomic Analysis of Human Brown Adipose Tissue Reveals Utilization of Coupled and Uncoupled Energy Expenditure Pathways |
title_sort | proteomic analysis of human brown adipose tissue reveals utilization of coupled and uncoupled energy expenditure pathways |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4945940/ https://www.ncbi.nlm.nih.gov/pubmed/27418403 http://dx.doi.org/10.1038/srep30030 |
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