Triiodothyronine activated extranuclear pathways upregulate adiponectin and leptin in murine adipocytes
Autor(a) principal: | |
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Data de Publicação: | 2020 |
Outros Autores: | , , , , , , , , |
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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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 |
|
_version_ |
1808128161998700544 |