'Sweetening' Pregnancy: Galectins at the Fetomaternal Interface

Autores
Blidner, A.G.; Rabinovich, G.A.
Año de publicación
2013
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Successful mammalian pregnancy relies upon acceptance of a semi-allogeneic fetus by the maternal immune system. Lessons learned from studies on protective immunity to microbial infections and tumours, prevention of autoimmunity, and allograft rejection have contributed to delineate the mechanisms leading to T-cell tolerance at the fetomaternal interface. Recent observations highlight the contribution of galectins, a family of endogenous glycan-binding proteins, to critical biological events occurring during mammalian gestation, including immune cell tolerance, inflammation, implantation, and angiogenesis. These multifunctional lectins can hierarchically control a cascade of immunoregulatory events including the expansion, recruitment, and function of regulatory T cells, the promotion of tolerogenic dendritic cells, and the execution of T-cell death programs. In addition, galectins can control cell adhesion and signaling events critical for implantation and are involved in fundamental processes linking tissue hypoxia to angiogenesis. In an attempt to integrate the regulatory roles of galectins to immunological and vascular programs operating during pregnancy. Here we outline the regulated expression and function of individual members of the galectin family within the fetoplacental unit and their biological implications for the development and preservation of successful pregnancies. © 2013 John Wiley & Sons A/S.
Fil:Blidner, A.G. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fuente
Am. J. Reprod. Immunol. 2013;69(4):369-382
Materia
Angiogenesis
Fetomaternal tolerance
Galectins
Immune privilege
Implantation
Pregnancy
ecalectin
galectin
galectin 1
galectin 10
galectin 12
galectin 13
galectin 14
galectin 15
galectin 2
galectin 3
galectin 4
galectin 7
galectin 8
glycan
hypoxia inducible factor 1alpha
immunoglobulin enhancer binding protein
Janus kinase 2
lectin
unclassified drug
vasculotropin receptor 3
fetoplacental unit
homeostasis
human
nonhuman
pregnancy
priority journal
protein expression
protein function
review
Cell Adhesion
Cell Communication
Cell Hypoxia
Dendritic Cells
Embryo Implantation
Female
Fetus
Galectins
Humans
Immune Tolerance
Neovascularization, Physiologic
Pregnancy
Signal Transduction
T-Lymphocytes, Regulatory
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_10467408_v69_n4_p369_Blidner

id BDUBAFCEN_3ac6de1b5b105a046f1216e061fa7d5c
oai_identifier_str paperaa:paper_10467408_v69_n4_p369_Blidner
network_acronym_str BDUBAFCEN
repository_id_str 1896
network_name_str Biblioteca Digital (UBA-FCEN)
spelling 'Sweetening' Pregnancy: Galectins at the Fetomaternal InterfaceBlidner, A.G.Rabinovich, G.A.AngiogenesisFetomaternal toleranceGalectinsImmune privilegeImplantationPregnancyecalectingalectingalectin 1galectin 10galectin 12galectin 13galectin 14galectin 15galectin 2galectin 3galectin 4galectin 7galectin 8glycanhypoxia inducible factor 1alphaimmunoglobulin enhancer binding proteinJanus kinase 2lectinunclassified drugvasculotropin receptor 3fetoplacental unithomeostasishumannonhumanpregnancypriority journalprotein expressionprotein functionreviewCell AdhesionCell CommunicationCell HypoxiaDendritic CellsEmbryo ImplantationFemaleFetusGalectinsHumansImmune ToleranceNeovascularization, PhysiologicPregnancySignal TransductionT-Lymphocytes, RegulatorySuccessful mammalian pregnancy relies upon acceptance of a semi-allogeneic fetus by the maternal immune system. Lessons learned from studies on protective immunity to microbial infections and tumours, prevention of autoimmunity, and allograft rejection have contributed to delineate the mechanisms leading to T-cell tolerance at the fetomaternal interface. Recent observations highlight the contribution of galectins, a family of endogenous glycan-binding proteins, to critical biological events occurring during mammalian gestation, including immune cell tolerance, inflammation, implantation, and angiogenesis. These multifunctional lectins can hierarchically control a cascade of immunoregulatory events including the expansion, recruitment, and function of regulatory T cells, the promotion of tolerogenic dendritic cells, and the execution of T-cell death programs. In addition, galectins can control cell adhesion and signaling events critical for implantation and are involved in fundamental processes linking tissue hypoxia to angiogenesis. In an attempt to integrate the regulatory roles of galectins to immunological and vascular programs operating during pregnancy. Here we outline the regulated expression and function of individual members of the galectin family within the fetoplacental unit and their biological implications for the development and preservation of successful pregnancies. © 2013 John Wiley & Sons A/S.Fil:Blidner, A.G. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.2013info: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_10467408_v69_n4_p369_BlidnerAm. J. Reprod. Immunol. 2013;69(4):369-382reponame: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/ar2025-09-11T10:21:44Zpaperaa:paper_10467408_v69_n4_p369_BlidnerInstitucionalhttps://digital.bl.fcen.uba.ar/Universidad públicaNo correspondehttps://digital.bl.fcen.uba.ar/cgi-bin/oaiserver.cgiana@bl.fcen.uba.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:18962025-09-11 10:21:45.605Biblioteca Digital (UBA-FCEN) - Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturalesfalse
dc.title.none.fl_str_mv 'Sweetening' Pregnancy: Galectins at the Fetomaternal Interface
title 'Sweetening' Pregnancy: Galectins at the Fetomaternal Interface
spellingShingle 'Sweetening' Pregnancy: Galectins at the Fetomaternal Interface
Blidner, A.G.
Angiogenesis
Fetomaternal tolerance
Galectins
Immune privilege
Implantation
Pregnancy
ecalectin
galectin
galectin 1
galectin 10
galectin 12
galectin 13
galectin 14
galectin 15
galectin 2
galectin 3
galectin 4
galectin 7
galectin 8
glycan
hypoxia inducible factor 1alpha
immunoglobulin enhancer binding protein
Janus kinase 2
lectin
unclassified drug
vasculotropin receptor 3
fetoplacental unit
homeostasis
human
nonhuman
pregnancy
priority journal
protein expression
protein function
review
Cell Adhesion
Cell Communication
Cell Hypoxia
Dendritic Cells
Embryo Implantation
Female
Fetus
Galectins
Humans
Immune Tolerance
Neovascularization, Physiologic
Pregnancy
Signal Transduction
T-Lymphocytes, Regulatory
title_short 'Sweetening' Pregnancy: Galectins at the Fetomaternal Interface
title_full 'Sweetening' Pregnancy: Galectins at the Fetomaternal Interface
title_fullStr 'Sweetening' Pregnancy: Galectins at the Fetomaternal Interface
title_full_unstemmed 'Sweetening' Pregnancy: Galectins at the Fetomaternal Interface
title_sort 'Sweetening' Pregnancy: Galectins at the Fetomaternal Interface
dc.creator.none.fl_str_mv Blidner, A.G.
Rabinovich, G.A.
author Blidner, A.G.
author_facet Blidner, A.G.
Rabinovich, G.A.
author_role author
author2 Rabinovich, G.A.
author2_role author
dc.subject.none.fl_str_mv Angiogenesis
Fetomaternal tolerance
Galectins
Immune privilege
Implantation
Pregnancy
ecalectin
galectin
galectin 1
galectin 10
galectin 12
galectin 13
galectin 14
galectin 15
galectin 2
galectin 3
galectin 4
galectin 7
galectin 8
glycan
hypoxia inducible factor 1alpha
immunoglobulin enhancer binding protein
Janus kinase 2
lectin
unclassified drug
vasculotropin receptor 3
fetoplacental unit
homeostasis
human
nonhuman
pregnancy
priority journal
protein expression
protein function
review
Cell Adhesion
Cell Communication
Cell Hypoxia
Dendritic Cells
Embryo Implantation
Female
Fetus
Galectins
Humans
Immune Tolerance
Neovascularization, Physiologic
Pregnancy
Signal Transduction
T-Lymphocytes, Regulatory
topic Angiogenesis
Fetomaternal tolerance
Galectins
Immune privilege
Implantation
Pregnancy
ecalectin
galectin
galectin 1
galectin 10
galectin 12
galectin 13
galectin 14
galectin 15
galectin 2
galectin 3
galectin 4
galectin 7
galectin 8
glycan
hypoxia inducible factor 1alpha
immunoglobulin enhancer binding protein
Janus kinase 2
lectin
unclassified drug
vasculotropin receptor 3
fetoplacental unit
homeostasis
human
nonhuman
pregnancy
priority journal
protein expression
protein function
review
Cell Adhesion
Cell Communication
Cell Hypoxia
Dendritic Cells
Embryo Implantation
Female
Fetus
Galectins
Humans
Immune Tolerance
Neovascularization, Physiologic
Pregnancy
Signal Transduction
T-Lymphocytes, Regulatory
dc.description.none.fl_txt_mv Successful mammalian pregnancy relies upon acceptance of a semi-allogeneic fetus by the maternal immune system. Lessons learned from studies on protective immunity to microbial infections and tumours, prevention of autoimmunity, and allograft rejection have contributed to delineate the mechanisms leading to T-cell tolerance at the fetomaternal interface. Recent observations highlight the contribution of galectins, a family of endogenous glycan-binding proteins, to critical biological events occurring during mammalian gestation, including immune cell tolerance, inflammation, implantation, and angiogenesis. These multifunctional lectins can hierarchically control a cascade of immunoregulatory events including the expansion, recruitment, and function of regulatory T cells, the promotion of tolerogenic dendritic cells, and the execution of T-cell death programs. In addition, galectins can control cell adhesion and signaling events critical for implantation and are involved in fundamental processes linking tissue hypoxia to angiogenesis. In an attempt to integrate the regulatory roles of galectins to immunological and vascular programs operating during pregnancy. Here we outline the regulated expression and function of individual members of the galectin family within the fetoplacental unit and their biological implications for the development and preservation of successful pregnancies. © 2013 John Wiley & Sons A/S.
Fil:Blidner, A.G. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
description Successful mammalian pregnancy relies upon acceptance of a semi-allogeneic fetus by the maternal immune system. Lessons learned from studies on protective immunity to microbial infections and tumours, prevention of autoimmunity, and allograft rejection have contributed to delineate the mechanisms leading to T-cell tolerance at the fetomaternal interface. Recent observations highlight the contribution of galectins, a family of endogenous glycan-binding proteins, to critical biological events occurring during mammalian gestation, including immune cell tolerance, inflammation, implantation, and angiogenesis. These multifunctional lectins can hierarchically control a cascade of immunoregulatory events including the expansion, recruitment, and function of regulatory T cells, the promotion of tolerogenic dendritic cells, and the execution of T-cell death programs. In addition, galectins can control cell adhesion and signaling events critical for implantation and are involved in fundamental processes linking tissue hypoxia to angiogenesis. In an attempt to integrate the regulatory roles of galectins to immunological and vascular programs operating during pregnancy. Here we outline the regulated expression and function of individual members of the galectin family within the fetoplacental unit and their biological implications for the development and preservation of successful pregnancies. © 2013 John Wiley & Sons A/S.
publishDate 2013
dc.date.none.fl_str_mv 2013
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_10467408_v69_n4_p369_Blidner
url http://hdl.handle.net/20.500.12110/paper_10467408_v69_n4_p369_Blidner
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 Am. J. Reprod. Immunol. 2013;69(4):369-382
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
_version_ 1842975011127689216
score 12.993085