Triiodothyronine activated extranuclear pathways upregulate adiponectin and leptin in murine adipocytes

Detalhes bibliográficos
Autor(a) principal: Mathias, Lucas Solla [UNESP]
Data de Publicação: 2020
Outros Autores: Rodrigues, Bruna Moretto [UNESP], Gonçalves, Bianca Mariani [UNESP], Moretto, Fernanda Cristina Fontes [UNESP], Olimpio, Regiane Marques Castro [UNESP], Deprá, Igor [UNESP], De Sibio, Maria Teresa [UNESP], Tilli, Helena Paim [UNESP], Nogueira, Célia Regina [UNESP], de Oliveira, Miriane [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.mce.2019.110690
http://hdl.handle.net/11449/201427
Resumo: Adiponectin and leptin, important for metabolic regulation, are synthesized and secreted by adipose tissue and are influenced by triiodothyronine (T3) that activates the MAPK/ERK and integrin αVβ3 pathways, modulating gene expression. Adipocytes were treated with T3 (10 nM), for 1 h, in the absence or presence of PD98059 (PD) and tetraiodothyroacetic acid (Tetrac), which are pathways inhibitors. The cells were incubated with Adipo Red/Oil Red O reagents, and intracellular lipid accumulation [glycerol and triacylglycerol (TAG)], MTT, 8-hydroxideoxyguanosine (8-OH-dG), and mRNA and protein expression were assessed. T3 increased leptin mRNA and protein expression, and, in contrast, there was a decrease in the Tetrac + T3 group. Adiponectin mRNA expression was not altered by T3, though it had increased its protein expression, which was terminated by inhibitors PD + T3 and Tetrac + T3. However, T3 did not alter PPARγ protein expression, lipid accumulation, TAG, glycerol, and DNA damage, but PD + T3 and Tetrac + T3 reduced these parameters. T3 activated the MAPK/ERK pathway on adipocytes to modulate the adiponectin protein expression and integrin αvβ3 to alter the leptin gene expression.
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spelling Triiodothyronine activated extranuclear pathways upregulate adiponectin and leptin in murine adipocytesAdiponectinIntegrin αVβ3LeptinLipidMAPK/ERKTriiodothyronineAdiponectin and leptin, important for metabolic regulation, are synthesized and secreted by adipose tissue and are influenced by triiodothyronine (T3) that activates the MAPK/ERK and integrin αVβ3 pathways, modulating gene expression. Adipocytes were treated with T3 (10 nM), for 1 h, in the absence or presence of PD98059 (PD) and tetraiodothyroacetic acid (Tetrac), which are pathways inhibitors. The cells were incubated with Adipo Red/Oil Red O reagents, and intracellular lipid accumulation [glycerol and triacylglycerol (TAG)], MTT, 8-hydroxideoxyguanosine (8-OH-dG), and mRNA and protein expression were assessed. T3 increased leptin mRNA and protein expression, and, in contrast, there was a decrease in the Tetrac + T3 group. Adiponectin mRNA expression was not altered by T3, though it had increased its protein expression, which was terminated by inhibitors PD + T3 and Tetrac + T3. However, T3 did not alter PPARγ protein expression, lipid accumulation, TAG, glycerol, and DNA damage, but PD + T3 and Tetrac + T3 reduced these parameters. T3 activated the MAPK/ERK pathway on adipocytes to modulate the adiponectin protein expression and integrin αvβ3 to alter the leptin gene expression.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)São Paulo State University (UNESP) Botucatu Medical SchoolSão Paulo State University (UNESP) Botucatu Medical SchoolFAPESP: 2010/16911-4Universidade Estadual Paulista (Unesp)Mathias, Lucas Solla [UNESP]Rodrigues, Bruna Moretto [UNESP]Gonçalves, Bianca Mariani [UNESP]Moretto, Fernanda Cristina Fontes [UNESP]Olimpio, Regiane Marques Castro [UNESP]Deprá, Igor [UNESP]De Sibio, Maria Teresa [UNESP]Tilli, Helena Paim [UNESP]Nogueira, Célia Regina [UNESP]de Oliveira, Miriane [UNESP]2020-12-12T02:32:13Z2020-12-12T02:32:13Z2020-03-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1016/j.mce.2019.110690Molecular and Cellular Endocrinology, v. 503.1872-80570303-7207http://hdl.handle.net/11449/20142710.1016/j.mce.2019.1106902-s2.0-85077037086Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengMolecular and Cellular Endocrinologyinfo:eu-repo/semantics/openAccess2024-08-14T17:23:21Zoai:repositorio.unesp.br:11449/201427Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-14T17:23:21Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Triiodothyronine activated extranuclear pathways upregulate adiponectin and leptin in murine adipocytes
title Triiodothyronine activated extranuclear pathways upregulate adiponectin and leptin in murine adipocytes
spellingShingle Triiodothyronine activated extranuclear pathways upregulate adiponectin and leptin in murine adipocytes
Mathias, Lucas Solla [UNESP]
Adiponectin
Integrin αVβ3
Leptin
Lipid
MAPK/ERK
Triiodothyronine
title_short Triiodothyronine activated extranuclear pathways upregulate adiponectin and leptin in murine adipocytes
title_full Triiodothyronine activated extranuclear pathways upregulate adiponectin and leptin in murine adipocytes
title_fullStr Triiodothyronine activated extranuclear pathways upregulate adiponectin and leptin in murine adipocytes
title_full_unstemmed Triiodothyronine activated extranuclear pathways upregulate adiponectin and leptin in murine adipocytes
title_sort Triiodothyronine activated extranuclear pathways upregulate adiponectin and leptin in murine adipocytes
author Mathias, Lucas Solla [UNESP]
author_facet Mathias, Lucas Solla [UNESP]
Rodrigues, Bruna Moretto [UNESP]
Gonçalves, Bianca Mariani [UNESP]
Moretto, Fernanda Cristina Fontes [UNESP]
Olimpio, Regiane Marques Castro [UNESP]
Deprá, Igor [UNESP]
De Sibio, Maria Teresa [UNESP]
Tilli, Helena Paim [UNESP]
Nogueira, Célia Regina [UNESP]
de Oliveira, Miriane [UNESP]
author_role author
author2 Rodrigues, Bruna Moretto [UNESP]
Gonçalves, Bianca Mariani [UNESP]
Moretto, Fernanda Cristina Fontes [UNESP]
Olimpio, Regiane Marques Castro [UNESP]
Deprá, Igor [UNESP]
De Sibio, Maria Teresa [UNESP]
Tilli, Helena Paim [UNESP]
Nogueira, Célia Regina [UNESP]
de Oliveira, Miriane [UNESP]
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Mathias, Lucas Solla [UNESP]
Rodrigues, Bruna Moretto [UNESP]
Gonçalves, Bianca Mariani [UNESP]
Moretto, Fernanda Cristina Fontes [UNESP]
Olimpio, Regiane Marques Castro [UNESP]
Deprá, Igor [UNESP]
De Sibio, Maria Teresa [UNESP]
Tilli, Helena Paim [UNESP]
Nogueira, Célia Regina [UNESP]
de Oliveira, Miriane [UNESP]
dc.subject.por.fl_str_mv Adiponectin
Integrin αVβ3
Leptin
Lipid
MAPK/ERK
Triiodothyronine
topic Adiponectin
Integrin αVβ3
Leptin
Lipid
MAPK/ERK
Triiodothyronine
description Adiponectin and leptin, important for metabolic regulation, are synthesized and secreted by adipose tissue and are influenced by triiodothyronine (T3) that activates the MAPK/ERK and integrin αVβ3 pathways, modulating gene expression. Adipocytes were treated with T3 (10 nM), for 1 h, in the absence or presence of PD98059 (PD) and tetraiodothyroacetic acid (Tetrac), which are pathways inhibitors. The cells were incubated with Adipo Red/Oil Red O reagents, and intracellular lipid accumulation [glycerol and triacylglycerol (TAG)], MTT, 8-hydroxideoxyguanosine (8-OH-dG), and mRNA and protein expression were assessed. T3 increased leptin mRNA and protein expression, and, in contrast, there was a decrease in the Tetrac + T3 group. Adiponectin mRNA expression was not altered by T3, though it had increased its protein expression, which was terminated by inhibitors PD + T3 and Tetrac + T3. However, T3 did not alter PPARγ protein expression, lipid accumulation, TAG, glycerol, and DNA damage, but PD + T3 and Tetrac + T3 reduced these parameters. T3 activated the MAPK/ERK pathway on adipocytes to modulate the adiponectin protein expression and integrin αvβ3 to alter the leptin gene expression.
publishDate 2020
dc.date.none.fl_str_mv 2020-12-12T02:32:13Z
2020-12-12T02:32:13Z
2020-03-01
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1016/j.mce.2019.110690
Molecular and Cellular Endocrinology, v. 503.
1872-8057
0303-7207
http://hdl.handle.net/11449/201427
10.1016/j.mce.2019.110690
2-s2.0-85077037086
url http://dx.doi.org/10.1016/j.mce.2019.110690
http://hdl.handle.net/11449/201427
identifier_str_mv Molecular and Cellular Endocrinology, v. 503.
1872-8057
0303-7207
10.1016/j.mce.2019.110690
2-s2.0-85077037086
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Molecular and Cellular Endocrinology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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