Leptin stimulates protein synthesis-activating translation machinery in human trophoblastic cells

Autores
Pérez-Pérez, A.; Julieta Maymo, Y.; Gambino, É.; Dueñas, J.L.; Goberna, R.; Varone, C.; Sánchez-Margalet, V.
Año de publicación
2009
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Leptin was originally considered as an adipocyte-derived signaling molecule for the central control of metabolism. However, pleiotropic effects of leptin have been identified in reproduction and pregnancy, particularly in placenta, where it may work as an autocrine hormone, mediating angiogenesis, growth, and immunomodulation. Leptin receptor (LEPR, also known as Ob-R) shows sequence homology to members of the class I cytokine receptor (gp130) superfamily. In fact, leptin may function as a proinflammatory cytokine. We have previously found that leptin is a trophic and mitogenic factor for trophoblastic cells. In order to further investigate the mechanism by which leptin stimulates cell growth in JEG-3 cells and trophoblastic cells, we studied the phosphorylation state of different proteins of the initiation stage of translation and the total protein synthesis by [3H]leucine incorporation in JEG-3 cells. We have found that leptin dose-dependently stimulates the phosphorylation and activation of the translation initiation factor EIF4E as well as the phosphorylation of the EIF4E binding protein EIF4EBP1 (PHAS-I), which releases EIF4E to form active complexes. Moreover, leptin dose-dependently stimulates protein synthesis, and this effect can be partially prevented by blocking mitogen-activated protein kinase (MAPK) and phosphatidylinositol 3 kinase (PIK3) pathways. In conclusion, leptin stimulates protein synthesis, at least in part activating the translation machinery, via the activation of MAPK and PIK3 pathways. © 2009 by the Society for the Study of Reproduction, Inc.
Fil:Julieta Maymo, Y. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fil:Gambino, É. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fil:Varone, C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fuente
Biol. Reprod. 2009;81(5):826-832
Materia
Leptin
Leptin receptor
Mechanisms of hormone action
Placenta
Trophoblast
initiation factor 4E
leptin
mitogen activated protein kinase
phosphatidylinositol 3 kinase
2 (2 amino 3 methoxyphenyl)chromone
androstane derivative
EIF4EBP1 protein, human
flavonoid
initiation factor 4E
leptin
mitogen activated protein kinase
phosphatidylinositol 3 kinase
phosphoprotein
protein kinase inhibitor
signal transducing adaptor protein
wortmannin
article
cell growth
controlled study
hormone action
human
human cell
priority journal
protein binding
protein phosphorylation
protein synthesis
translation initiation
trophoblast
analysis of variance
cell culture
cell line
dose response
drug effect
female
metabolism
phosphorylation
physiology
placenta
pregnancy
protein synthesis
signal transduction
Western blotting
1-Phosphatidylinositol 3-Kinase
Adaptor Proteins, Signal Transducing
Analysis of Variance
Androstadienes
Blotting, Western
Cell Line
Cells, Cultured
Dose-Response Relationship, Drug
Eukaryotic Initiation Factor-4E
Female
Flavonoids
Humans
Leptin
Mitogen-Activated Protein Kinases
Phosphoproteins
Phosphorylation
Placenta
Pregnancy
Protein Biosynthesis
Protein Kinase Inhibitors
Signal Transduction
Trophoblasts
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by/2.5/ar
Repositorio
Biblioteca Digital (UBA-FCEN)
Institución
Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
OAI Identificador
paperaa:paper_00063363_v81_n5_p826_PerezPerez

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oai_identifier_str paperaa:paper_00063363_v81_n5_p826_PerezPerez
network_acronym_str BDUBAFCEN
repository_id_str 1896
network_name_str Biblioteca Digital (UBA-FCEN)
spelling Leptin stimulates protein synthesis-activating translation machinery in human trophoblastic cellsPérez-Pérez, A.Julieta Maymo, Y.Gambino, É.Dueñas, J.L.Goberna, R.Varone, C.Sánchez-Margalet, V.LeptinLeptin receptorMechanisms of hormone actionPlacentaTrophoblastinitiation factor 4Eleptinmitogen activated protein kinasephosphatidylinositol 3 kinase2 (2 amino 3 methoxyphenyl)chromoneandrostane derivativeEIF4EBP1 protein, humanflavonoidinitiation factor 4Eleptinmitogen activated protein kinasephosphatidylinositol 3 kinasephosphoproteinprotein kinase inhibitorsignal transducing adaptor proteinwortmanninarticlecell growthcontrolled studyhormone actionhumanhuman cellpriority journalprotein bindingprotein phosphorylationprotein synthesistranslation initiationtrophoblastanalysis of variancecell culturecell linedose responsedrug effectfemalemetabolismphosphorylationphysiologyplacentapregnancyprotein synthesissignal transductionWestern blotting1-Phosphatidylinositol 3-KinaseAdaptor Proteins, Signal TransducingAnalysis of VarianceAndrostadienesBlotting, WesternCell LineCells, CulturedDose-Response Relationship, DrugEukaryotic Initiation Factor-4EFemaleFlavonoidsHumansLeptinMitogen-Activated Protein KinasesPhosphoproteinsPhosphorylationPlacentaPregnancyProtein BiosynthesisProtein Kinase InhibitorsSignal TransductionTrophoblastsLeptin was originally considered as an adipocyte-derived signaling molecule for the central control of metabolism. However, pleiotropic effects of leptin have been identified in reproduction and pregnancy, particularly in placenta, where it may work as an autocrine hormone, mediating angiogenesis, growth, and immunomodulation. Leptin receptor (LEPR, also known as Ob-R) shows sequence homology to members of the class I cytokine receptor (gp130) superfamily. In fact, leptin may function as a proinflammatory cytokine. We have previously found that leptin is a trophic and mitogenic factor for trophoblastic cells. In order to further investigate the mechanism by which leptin stimulates cell growth in JEG-3 cells and trophoblastic cells, we studied the phosphorylation state of different proteins of the initiation stage of translation and the total protein synthesis by [3H]leucine incorporation in JEG-3 cells. We have found that leptin dose-dependently stimulates the phosphorylation and activation of the translation initiation factor EIF4E as well as the phosphorylation of the EIF4E binding protein EIF4EBP1 (PHAS-I), which releases EIF4E to form active complexes. Moreover, leptin dose-dependently stimulates protein synthesis, and this effect can be partially prevented by blocking mitogen-activated protein kinase (MAPK) and phosphatidylinositol 3 kinase (PIK3) pathways. In conclusion, leptin stimulates protein synthesis, at least in part activating the translation machinery, via the activation of MAPK and PIK3 pathways. © 2009 by the Society for the Study of Reproduction, Inc.Fil:Julieta Maymo, Y. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.Fil:Gambino, É. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.Fil:Varone, C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.2009info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfhttp://hdl.handle.net/20.500.12110/paper_00063363_v81_n5_p826_PerezPerezBiol. Reprod. 2009;81(5):826-832reponame:Biblioteca Digital (UBA-FCEN)instname:Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturalesinstacron:UBA-FCENenginfo:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/2.5/ar2025-09-04T09:48:40Zpaperaa:paper_00063363_v81_n5_p826_PerezPerezInstitucionalhttps://digital.bl.fcen.uba.ar/Universidad públicaNo correspondehttps://digital.bl.fcen.uba.ar/cgi-bin/oaiserver.cgiana@bl.fcen.uba.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:18962025-09-04 09:48:42.856Biblioteca Digital (UBA-FCEN) - Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturalesfalse
dc.title.none.fl_str_mv Leptin stimulates protein synthesis-activating translation machinery in human trophoblastic cells
title Leptin stimulates protein synthesis-activating translation machinery in human trophoblastic cells
spellingShingle Leptin stimulates protein synthesis-activating translation machinery in human trophoblastic cells
Pérez-Pérez, A.
Leptin
Leptin receptor
Mechanisms of hormone action
Placenta
Trophoblast
initiation factor 4E
leptin
mitogen activated protein kinase
phosphatidylinositol 3 kinase
2 (2 amino 3 methoxyphenyl)chromone
androstane derivative
EIF4EBP1 protein, human
flavonoid
initiation factor 4E
leptin
mitogen activated protein kinase
phosphatidylinositol 3 kinase
phosphoprotein
protein kinase inhibitor
signal transducing adaptor protein
wortmannin
article
cell growth
controlled study
hormone action
human
human cell
priority journal
protein binding
protein phosphorylation
protein synthesis
translation initiation
trophoblast
analysis of variance
cell culture
cell line
dose response
drug effect
female
metabolism
phosphorylation
physiology
placenta
pregnancy
protein synthesis
signal transduction
Western blotting
1-Phosphatidylinositol 3-Kinase
Adaptor Proteins, Signal Transducing
Analysis of Variance
Androstadienes
Blotting, Western
Cell Line
Cells, Cultured
Dose-Response Relationship, Drug
Eukaryotic Initiation Factor-4E
Female
Flavonoids
Humans
Leptin
Mitogen-Activated Protein Kinases
Phosphoproteins
Phosphorylation
Placenta
Pregnancy
Protein Biosynthesis
Protein Kinase Inhibitors
Signal Transduction
Trophoblasts
title_short Leptin stimulates protein synthesis-activating translation machinery in human trophoblastic cells
title_full Leptin stimulates protein synthesis-activating translation machinery in human trophoblastic cells
title_fullStr Leptin stimulates protein synthesis-activating translation machinery in human trophoblastic cells
title_full_unstemmed Leptin stimulates protein synthesis-activating translation machinery in human trophoblastic cells
title_sort Leptin stimulates protein synthesis-activating translation machinery in human trophoblastic cells
dc.creator.none.fl_str_mv Pérez-Pérez, A.
Julieta Maymo, Y.
Gambino, É.
Dueñas, J.L.
Goberna, R.
Varone, C.
Sánchez-Margalet, V.
author Pérez-Pérez, A.
author_facet Pérez-Pérez, A.
Julieta Maymo, Y.
Gambino, É.
Dueñas, J.L.
Goberna, R.
Varone, C.
Sánchez-Margalet, V.
author_role author
author2 Julieta Maymo, Y.
Gambino, É.
Dueñas, J.L.
Goberna, R.
Varone, C.
Sánchez-Margalet, V.
author2_role author
author
author
author
author
author
dc.subject.none.fl_str_mv Leptin
Leptin receptor
Mechanisms of hormone action
Placenta
Trophoblast
initiation factor 4E
leptin
mitogen activated protein kinase
phosphatidylinositol 3 kinase
2 (2 amino 3 methoxyphenyl)chromone
androstane derivative
EIF4EBP1 protein, human
flavonoid
initiation factor 4E
leptin
mitogen activated protein kinase
phosphatidylinositol 3 kinase
phosphoprotein
protein kinase inhibitor
signal transducing adaptor protein
wortmannin
article
cell growth
controlled study
hormone action
human
human cell
priority journal
protein binding
protein phosphorylation
protein synthesis
translation initiation
trophoblast
analysis of variance
cell culture
cell line
dose response
drug effect
female
metabolism
phosphorylation
physiology
placenta
pregnancy
protein synthesis
signal transduction
Western blotting
1-Phosphatidylinositol 3-Kinase
Adaptor Proteins, Signal Transducing
Analysis of Variance
Androstadienes
Blotting, Western
Cell Line
Cells, Cultured
Dose-Response Relationship, Drug
Eukaryotic Initiation Factor-4E
Female
Flavonoids
Humans
Leptin
Mitogen-Activated Protein Kinases
Phosphoproteins
Phosphorylation
Placenta
Pregnancy
Protein Biosynthesis
Protein Kinase Inhibitors
Signal Transduction
Trophoblasts
topic Leptin
Leptin receptor
Mechanisms of hormone action
Placenta
Trophoblast
initiation factor 4E
leptin
mitogen activated protein kinase
phosphatidylinositol 3 kinase
2 (2 amino 3 methoxyphenyl)chromone
androstane derivative
EIF4EBP1 protein, human
flavonoid
initiation factor 4E
leptin
mitogen activated protein kinase
phosphatidylinositol 3 kinase
phosphoprotein
protein kinase inhibitor
signal transducing adaptor protein
wortmannin
article
cell growth
controlled study
hormone action
human
human cell
priority journal
protein binding
protein phosphorylation
protein synthesis
translation initiation
trophoblast
analysis of variance
cell culture
cell line
dose response
drug effect
female
metabolism
phosphorylation
physiology
placenta
pregnancy
protein synthesis
signal transduction
Western blotting
1-Phosphatidylinositol 3-Kinase
Adaptor Proteins, Signal Transducing
Analysis of Variance
Androstadienes
Blotting, Western
Cell Line
Cells, Cultured
Dose-Response Relationship, Drug
Eukaryotic Initiation Factor-4E
Female
Flavonoids
Humans
Leptin
Mitogen-Activated Protein Kinases
Phosphoproteins
Phosphorylation
Placenta
Pregnancy
Protein Biosynthesis
Protein Kinase Inhibitors
Signal Transduction
Trophoblasts
dc.description.none.fl_txt_mv Leptin was originally considered as an adipocyte-derived signaling molecule for the central control of metabolism. However, pleiotropic effects of leptin have been identified in reproduction and pregnancy, particularly in placenta, where it may work as an autocrine hormone, mediating angiogenesis, growth, and immunomodulation. Leptin receptor (LEPR, also known as Ob-R) shows sequence homology to members of the class I cytokine receptor (gp130) superfamily. In fact, leptin may function as a proinflammatory cytokine. We have previously found that leptin is a trophic and mitogenic factor for trophoblastic cells. In order to further investigate the mechanism by which leptin stimulates cell growth in JEG-3 cells and trophoblastic cells, we studied the phosphorylation state of different proteins of the initiation stage of translation and the total protein synthesis by [3H]leucine incorporation in JEG-3 cells. We have found that leptin dose-dependently stimulates the phosphorylation and activation of the translation initiation factor EIF4E as well as the phosphorylation of the EIF4E binding protein EIF4EBP1 (PHAS-I), which releases EIF4E to form active complexes. Moreover, leptin dose-dependently stimulates protein synthesis, and this effect can be partially prevented by blocking mitogen-activated protein kinase (MAPK) and phosphatidylinositol 3 kinase (PIK3) pathways. In conclusion, leptin stimulates protein synthesis, at least in part activating the translation machinery, via the activation of MAPK and PIK3 pathways. © 2009 by the Society for the Study of Reproduction, Inc.
Fil:Julieta Maymo, Y. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fil:Gambino, É. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fil:Varone, C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
description Leptin was originally considered as an adipocyte-derived signaling molecule for the central control of metabolism. However, pleiotropic effects of leptin have been identified in reproduction and pregnancy, particularly in placenta, where it may work as an autocrine hormone, mediating angiogenesis, growth, and immunomodulation. Leptin receptor (LEPR, also known as Ob-R) shows sequence homology to members of the class I cytokine receptor (gp130) superfamily. In fact, leptin may function as a proinflammatory cytokine. We have previously found that leptin is a trophic and mitogenic factor for trophoblastic cells. In order to further investigate the mechanism by which leptin stimulates cell growth in JEG-3 cells and trophoblastic cells, we studied the phosphorylation state of different proteins of the initiation stage of translation and the total protein synthesis by [3H]leucine incorporation in JEG-3 cells. We have found that leptin dose-dependently stimulates the phosphorylation and activation of the translation initiation factor EIF4E as well as the phosphorylation of the EIF4E binding protein EIF4EBP1 (PHAS-I), which releases EIF4E to form active complexes. Moreover, leptin dose-dependently stimulates protein synthesis, and this effect can be partially prevented by blocking mitogen-activated protein kinase (MAPK) and phosphatidylinositol 3 kinase (PIK3) pathways. In conclusion, leptin stimulates protein synthesis, at least in part activating the translation machinery, via the activation of MAPK and PIK3 pathways. © 2009 by the Society for the Study of Reproduction, Inc.
publishDate 2009
dc.date.none.fl_str_mv 2009
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/20.500.12110/paper_00063363_v81_n5_p826_PerezPerez
url http://hdl.handle.net/20.500.12110/paper_00063363_v81_n5_p826_PerezPerez
dc.language.none.fl_str_mv eng
language eng
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by/2.5/ar
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by/2.5/ar
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv Biol. Reprod. 2009;81(5):826-832
reponame:Biblioteca Digital (UBA-FCEN)
instname:Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
instacron:UBA-FCEN
reponame_str Biblioteca Digital (UBA-FCEN)
collection Biblioteca Digital (UBA-FCEN)
instname_str Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
instacron_str UBA-FCEN
institution UBA-FCEN
repository.name.fl_str_mv Biblioteca Digital (UBA-FCEN) - Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
repository.mail.fl_str_mv ana@bl.fcen.uba.ar
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