'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
- Institución
- Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
- OAI Identificador
- paperaa:paper_10467408_v69_n4_p369_Blidner
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'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 |
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1842975011127689216 |
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12.993085 |