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Exercise training remodels inguinal white adipose tissue through adaptations in innervation, vascularization, and the extracellular matrix
Inguinal white adipose tissue (iWAT) is essential for the beneficial effects of exercise training on metabolic health. The underlying mechanisms for these effects are not fully understood, and here, we test the hypothesis that exercise training results in a more favorable iWAT structural phenotype....
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10374102/ https://www.ncbi.nlm.nih.gov/pubmed/37058410 http://dx.doi.org/10.1016/j.celrep.2023.112392 |
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author | Nigro, Pasquale Vamvini, Maria Yang, Jiekun Caputo, Tiziana Ho, Li-Lun Carbone, Nicholas P. Papadopoulos, Danae Conlin, Royce He, Jie Hirshman, Michael F. White, Joseph D. Robidoux, Jacques Hickner, Robert C. Nielsen, Søren Pedersen, Bente K. Kellis, Manolis Middelbeek, Roeland J.W. Goodyear, Laurie J. |
author_facet | Nigro, Pasquale Vamvini, Maria Yang, Jiekun Caputo, Tiziana Ho, Li-Lun Carbone, Nicholas P. Papadopoulos, Danae Conlin, Royce He, Jie Hirshman, Michael F. White, Joseph D. Robidoux, Jacques Hickner, Robert C. Nielsen, Søren Pedersen, Bente K. Kellis, Manolis Middelbeek, Roeland J.W. Goodyear, Laurie J. |
author_sort | Nigro, Pasquale |
collection | PubMed |
description | Inguinal white adipose tissue (iWAT) is essential for the beneficial effects of exercise training on metabolic health. The underlying mechanisms for these effects are not fully understood, and here, we test the hypothesis that exercise training results in a more favorable iWAT structural phenotype. Using biochemical, imaging, and multi-omics analyses, we find that 11 days of wheel running in male mice causes profound iWAT remodeling including decreased extracellular matrix (ECM) deposition and increased vascularization and innervation. We identify adipose stem cells as one of the main contributors to training-induced ECM remodeling, show that the PRDM16 transcriptional complex is necessary for iWAT remodeling and beiging, and discover neuronal growth regulator 1 (NEGR1) as a link between PRDM16 and neuritogenesis. Moreover, we find that training causes a shift from hypertrophic to insulin-sensitive adipocyte subpopulations. Exercise training leads to remarkable adaptations to iWAT structure and cell-type composition that can confer beneficial changes in tissue metabolism. |
format | Online Article Text |
id | pubmed-10374102 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
record_format | MEDLINE/PubMed |
spelling | pubmed-103741022023-07-27 Exercise training remodels inguinal white adipose tissue through adaptations in innervation, vascularization, and the extracellular matrix Nigro, Pasquale Vamvini, Maria Yang, Jiekun Caputo, Tiziana Ho, Li-Lun Carbone, Nicholas P. Papadopoulos, Danae Conlin, Royce He, Jie Hirshman, Michael F. White, Joseph D. Robidoux, Jacques Hickner, Robert C. Nielsen, Søren Pedersen, Bente K. Kellis, Manolis Middelbeek, Roeland J.W. Goodyear, Laurie J. Cell Rep Article Inguinal white adipose tissue (iWAT) is essential for the beneficial effects of exercise training on metabolic health. The underlying mechanisms for these effects are not fully understood, and here, we test the hypothesis that exercise training results in a more favorable iWAT structural phenotype. Using biochemical, imaging, and multi-omics analyses, we find that 11 days of wheel running in male mice causes profound iWAT remodeling including decreased extracellular matrix (ECM) deposition and increased vascularization and innervation. We identify adipose stem cells as one of the main contributors to training-induced ECM remodeling, show that the PRDM16 transcriptional complex is necessary for iWAT remodeling and beiging, and discover neuronal growth regulator 1 (NEGR1) as a link between PRDM16 and neuritogenesis. Moreover, we find that training causes a shift from hypertrophic to insulin-sensitive adipocyte subpopulations. Exercise training leads to remarkable adaptations to iWAT structure and cell-type composition that can confer beneficial changes in tissue metabolism. 2023-04-25 2023-04-13 /pmc/articles/PMC10374102/ /pubmed/37058410 http://dx.doi.org/10.1016/j.celrep.2023.112392 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ). |
spellingShingle | Article Nigro, Pasquale Vamvini, Maria Yang, Jiekun Caputo, Tiziana Ho, Li-Lun Carbone, Nicholas P. Papadopoulos, Danae Conlin, Royce He, Jie Hirshman, Michael F. White, Joseph D. Robidoux, Jacques Hickner, Robert C. Nielsen, Søren Pedersen, Bente K. Kellis, Manolis Middelbeek, Roeland J.W. Goodyear, Laurie J. Exercise training remodels inguinal white adipose tissue through adaptations in innervation, vascularization, and the extracellular matrix |
title | Exercise training remodels inguinal white adipose tissue through adaptations in innervation, vascularization, and the extracellular matrix |
title_full | Exercise training remodels inguinal white adipose tissue through adaptations in innervation, vascularization, and the extracellular matrix |
title_fullStr | Exercise training remodels inguinal white adipose tissue through adaptations in innervation, vascularization, and the extracellular matrix |
title_full_unstemmed | Exercise training remodels inguinal white adipose tissue through adaptations in innervation, vascularization, and the extracellular matrix |
title_short | Exercise training remodels inguinal white adipose tissue through adaptations in innervation, vascularization, and the extracellular matrix |
title_sort | exercise training remodels inguinal white adipose tissue through adaptations in innervation, vascularization, and the extracellular matrix |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10374102/ https://www.ncbi.nlm.nih.gov/pubmed/37058410 http://dx.doi.org/10.1016/j.celrep.2023.112392 |
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