FGF15/19 is required for adipose tissue plasticity in response to thermogenic adaptations
Objective To determine the role of enterokine FGF15/19 in adipose tissue thermogenic adaptations. Methods Circulating FGF19 and gene expression (qRT-PCR) levels were assessed in subcutaneous adipose tissue from obese human patients. Effects of experimentally increased FGF15 and FGF19 levels in vivo...
| Autores: | , , , , , , , , , |
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| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2021 |
| País: | España |
| Institución: | Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
| Repositorio: | Recercat. Dipósit de la Recerca de Catalunya |
| OAI Identifier: | oai:recercat.cat:10256/21300 |
| Acceso en línea: | http://hdl.handle.net/10256/21300 |
| Access Level: | acceso abierto |
| Palabra clave: | Teixit adipós Adipose tissues |
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FGF15/19 is required for adipose tissue plasticity in response to thermogenic adaptationsMorón-Ros, SamanthaUriarte, IkerBerasain, CarmenAvila, Matías AntonioSabater Masdeu, MònicaMoreno Navarrete, José MaríaFernández-Real Lemos, José ManuelGiralt i Oms, MartaVillarroya, FrancescGavaldà i Navarro, AleixTeixit adipósAdipose tissuesObjective To determine the role of enterokine FGF15/19 in adipose tissue thermogenic adaptations. Methods Circulating FGF19 and gene expression (qRT-PCR) levels were assessed in subcutaneous adipose tissue from obese human patients. Effects of experimentally increased FGF15 and FGF19 levels in vivo were determined in mice using adenoviral and adeno-associated vectors. Adipose tissues were characterized in FGF15-null mice under distinct cold-related thermogenic challenges. The analyses spanned metabolic profiling, tissue characterization, histology, gene expression, and immunoblot assays. Results In humans, FGF19 levels are directly associated with UCP1 gene expression in subcutaneous adipose tissue. Experimental increases in FGF15 or FGF19 induced white fat browning in mice as demonstrated by the appearance of multilocular beige cells and markers indicative of a beige phenotype, including increased UCP1 protein levels. Mice lacking FGF15 showed markedly impaired white adipose tissue browning and a mild reduction in parameters indicative of BAT activity in response to cold-induced environmental thermogenic challenges. This was concomitant with signs of altered systemic metabolism, such as reduced glucose tolerance and impaired cold-induced insulin sensitizationFunding from the Ministry of Science and Innovation (SAF2017-85722R); Health Research Fund, Carlos III Health Institute (PI17-00420), co-financed by the European Regional Development Fund (ERDF); the Marató de TV3 Foundation (201612-30/31); the Fundación Bancaria La Caixa (Hepacare Project); the M. Torres Foundation; and the Eugenio Rodriguez Pascual Foundation (to IU, CB, and MAA) is acknowledgedElsevier2021info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionpeer-reviewedapplication/pdfhttp://hdl.handle.net/10256/21300Molecular Metabolism, 2021, vol. 43, art.núm. 101113Articles publicats (IdIBGi)reponame:Recercat. Dipósit de la Recerca de Catalunyainstname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)Inglésinfo:eu-repo/semantics/altIdentifier/doi/10.1016/j.molmet.2020.101113info:eu-repo/semantics/altIdentifier/eissn/2212-8778Attribution-NonCommercial-NoDerivatives 4.0 Internationalhttp://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessoai:recercat.cat:10256/213002026-05-29T05:05:01Z |
| dc.title.none.fl_str_mv |
FGF15/19 is required for adipose tissue plasticity in response to thermogenic adaptations |
| title |
FGF15/19 is required for adipose tissue plasticity in response to thermogenic adaptations |
| spellingShingle |
FGF15/19 is required for adipose tissue plasticity in response to thermogenic adaptations Morón-Ros, Samantha Teixit adipós Adipose tissues |
| title_short |
FGF15/19 is required for adipose tissue plasticity in response to thermogenic adaptations |
| title_full |
FGF15/19 is required for adipose tissue plasticity in response to thermogenic adaptations |
| title_fullStr |
FGF15/19 is required for adipose tissue plasticity in response to thermogenic adaptations |
| title_full_unstemmed |
FGF15/19 is required for adipose tissue plasticity in response to thermogenic adaptations |
| title_sort |
FGF15/19 is required for adipose tissue plasticity in response to thermogenic adaptations |
| dc.creator.none.fl_str_mv |
Morón-Ros, Samantha Uriarte, Iker Berasain, Carmen Avila, Matías Antonio Sabater Masdeu, Mònica Moreno Navarrete, José María Fernández-Real Lemos, José Manuel Giralt i Oms, Marta Villarroya, Francesc Gavaldà i Navarro, Aleix |
| author |
Morón-Ros, Samantha |
| author_facet |
Morón-Ros, Samantha Uriarte, Iker Berasain, Carmen Avila, Matías Antonio Sabater Masdeu, Mònica Moreno Navarrete, José María Fernández-Real Lemos, José Manuel Giralt i Oms, Marta Villarroya, Francesc Gavaldà i Navarro, Aleix |
| author_role |
author |
| author2 |
Uriarte, Iker Berasain, Carmen Avila, Matías Antonio Sabater Masdeu, Mònica Moreno Navarrete, José María Fernández-Real Lemos, José Manuel Giralt i Oms, Marta Villarroya, Francesc Gavaldà i Navarro, Aleix |
| author2_role |
author author author author author author author author author |
| dc.subject.none.fl_str_mv |
Teixit adipós Adipose tissues |
| topic |
Teixit adipós Adipose tissues |
| description |
Objective To determine the role of enterokine FGF15/19 in adipose tissue thermogenic adaptations. Methods Circulating FGF19 and gene expression (qRT-PCR) levels were assessed in subcutaneous adipose tissue from obese human patients. Effects of experimentally increased FGF15 and FGF19 levels in vivo were determined in mice using adenoviral and adeno-associated vectors. Adipose tissues were characterized in FGF15-null mice under distinct cold-related thermogenic challenges. The analyses spanned metabolic profiling, tissue characterization, histology, gene expression, and immunoblot assays. Results In humans, FGF19 levels are directly associated with UCP1 gene expression in subcutaneous adipose tissue. Experimental increases in FGF15 or FGF19 induced white fat browning in mice as demonstrated by the appearance of multilocular beige cells and markers indicative of a beige phenotype, including increased UCP1 protein levels. Mice lacking FGF15 showed markedly impaired white adipose tissue browning and a mild reduction in parameters indicative of BAT activity in response to cold-induced environmental thermogenic challenges. This was concomitant with signs of altered systemic metabolism, such as reduced glucose tolerance and impaired cold-induced insulin sensitization |
| publishDate |
2021 |
| dc.date.none.fl_str_mv |
2021 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion peer-reviewed |
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article |
| status_str |
publishedVersion |
| dc.identifier.none.fl_str_mv |
http://hdl.handle.net/10256/21300 |
| url |
http://hdl.handle.net/10256/21300 |
| dc.language.none.fl_str_mv |
Inglés |
| language_invalid_str_mv |
Inglés |
| dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.molmet.2020.101113 info:eu-repo/semantics/altIdentifier/eissn/2212-8778 |
| dc.rights.none.fl_str_mv |
Attribution-NonCommercial-NoDerivatives 4.0 International http://creativecommons.org/licenses/by-nc-nd/4.0/ info:eu-repo/semantics/openAccess |
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Attribution-NonCommercial-NoDerivatives 4.0 International http://creativecommons.org/licenses/by-nc-nd/4.0/ |
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openAccess |
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application/pdf |
| dc.publisher.none.fl_str_mv |
Elsevier |
| publisher.none.fl_str_mv |
Elsevier |
| dc.source.none.fl_str_mv |
Molecular Metabolism, 2021, vol. 43, art.núm. 101113 Articles publicats (IdIBGi) reponame:Recercat. Dipósit de la Recerca de Catalunya instname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
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Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
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Recercat. Dipósit de la Recerca de Catalunya |
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Recercat. Dipósit de la Recerca de Catalunya |
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