Uterine NK Cells Are Critical in Shaping DC Immunogenic Functions Compatible with Pregnancy Progression

Autores
González, I.T.; Barrientos, G.; Freitag, N.; Otto, T.; Thijssen, V.L.J.L.; Moschansky, P.; von Kwiatkowski, P.; Klapp, B.F.; Winterhager, E.; Bauersachs, S.; Blois, S.M.
Año de publicación
2012
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Dendritic cell (DC) and natural killer (NK) cell interactions are important for the regulation of innate and adaptive immunity, but their relevance during early pregnancy remains elusive. Using two different strategies to manipulate the frequency of NK cells and DC during gestation, we investigated their relative impact on the decidualization process and on angiogenic responses that characterize murine implantation. Manipulation of the frequency of NK cells, DC or both lead to a defective decidual response characterized by decreased proliferation and differentiation of stromal cells. Whereas no detrimental effects were evident upon expansion of DC, NK cell ablation in such expanded DC mice severely compromised decidual development and led to early pregnancy loss. Pregnancy failure in these mice was associated with an unbalanced production of anti-angiogenic signals and most notably, with increased expression of genes related to inflammation and immunogenic activation of DC. Thus, NK cells appear to play an important role counteracting potential anomalies raised by DC expansion and overactivity in the decidua, becoming critical for normal pregnancy progression. © 2012 González et al.
Fuente
PLoS ONE 2012;7(10)
Materia
angiopoietin 1
glycoprotein p 15095
animal cell
animal tissue
article
cell differentiation
cell expansion
cell interaction
cell proliferation
cell shape
controlled study
decidualization
dendritic cell
female
first trimester pregnancy
flow cytometry
fluorescence activated cell sorting
gene expression
histopathology
immunogenicity
immunohistochemistry
inflammation
mouse
natural killer cell
nidation
nonhuman
pregnancy
pregnancy disorder
quantitative analysis
reverse transcription polymerase chain reaction
stroma cell
T cell depletion
uterine cervix
Animals
Dendritic Cells
Enzyme-Linked Immunosorbent Assay
Female
Immunohistochemistry
Killer Cells, Natural
Male
Mice
Oligonucleotide Array Sequence Analysis
Pregnancy
Reverse Transcriptase Polymerase Chain Reaction
Uterus
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_19326203_v7_n10_p_Gonzalez

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oai_identifier_str paperaa:paper_19326203_v7_n10_p_Gonzalez
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repository_id_str 1896
network_name_str Biblioteca Digital (UBA-FCEN)
spelling Uterine NK Cells Are Critical in Shaping DC Immunogenic Functions Compatible with Pregnancy ProgressionGonzález, I.T.Barrientos, G.Freitag, N.Otto, T.Thijssen, V.L.J.L.Moschansky, P.von Kwiatkowski, P.Klapp, B.F.Winterhager, E.Bauersachs, S.Blois, S.M.angiopoietin 1glycoprotein p 15095animal cellanimal tissuearticlecell differentiationcell expansioncell interactioncell proliferationcell shapecontrolled studydecidualizationdendritic cellfemalefirst trimester pregnancyflow cytometryfluorescence activated cell sortinggene expressionhistopathologyimmunogenicityimmunohistochemistryinflammationmousenatural killer cellnidationnonhumanpregnancypregnancy disorderquantitative analysisreverse transcription polymerase chain reactionstroma cellT cell depletionuterine cervixAnimalsDendritic CellsEnzyme-Linked Immunosorbent AssayFemaleImmunohistochemistryKiller Cells, NaturalMaleMiceOligonucleotide Array Sequence AnalysisPregnancyReverse Transcriptase Polymerase Chain ReactionUterusDendritic cell (DC) and natural killer (NK) cell interactions are important for the regulation of innate and adaptive immunity, but their relevance during early pregnancy remains elusive. Using two different strategies to manipulate the frequency of NK cells and DC during gestation, we investigated their relative impact on the decidualization process and on angiogenic responses that characterize murine implantation. Manipulation of the frequency of NK cells, DC or both lead to a defective decidual response characterized by decreased proliferation and differentiation of stromal cells. Whereas no detrimental effects were evident upon expansion of DC, NK cell ablation in such expanded DC mice severely compromised decidual development and led to early pregnancy loss. Pregnancy failure in these mice was associated with an unbalanced production of anti-angiogenic signals and most notably, with increased expression of genes related to inflammation and immunogenic activation of DC. Thus, NK cells appear to play an important role counteracting potential anomalies raised by DC expansion and overactivity in the decidua, becoming critical for normal pregnancy progression. © 2012 González et al.2012info: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_19326203_v7_n10_p_GonzalezPLoS ONE 2012;7(10)reponame: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/ar2025-10-16T09:30:06Zpaperaa:paper_19326203_v7_n10_p_GonzalezInstitucionalhttps://digital.bl.fcen.uba.ar/Universidad públicaNo correspondehttps://digital.bl.fcen.uba.ar/cgi-bin/oaiserver.cgiana@bl.fcen.uba.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:18962025-10-16 09:30:08.019Biblioteca Digital (UBA-FCEN) - Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturalesfalse
dc.title.none.fl_str_mv Uterine NK Cells Are Critical in Shaping DC Immunogenic Functions Compatible with Pregnancy Progression
title Uterine NK Cells Are Critical in Shaping DC Immunogenic Functions Compatible with Pregnancy Progression
spellingShingle Uterine NK Cells Are Critical in Shaping DC Immunogenic Functions Compatible with Pregnancy Progression
González, I.T.
angiopoietin 1
glycoprotein p 15095
animal cell
animal tissue
article
cell differentiation
cell expansion
cell interaction
cell proliferation
cell shape
controlled study
decidualization
dendritic cell
female
first trimester pregnancy
flow cytometry
fluorescence activated cell sorting
gene expression
histopathology
immunogenicity
immunohistochemistry
inflammation
mouse
natural killer cell
nidation
nonhuman
pregnancy
pregnancy disorder
quantitative analysis
reverse transcription polymerase chain reaction
stroma cell
T cell depletion
uterine cervix
Animals
Dendritic Cells
Enzyme-Linked Immunosorbent Assay
Female
Immunohistochemistry
Killer Cells, Natural
Male
Mice
Oligonucleotide Array Sequence Analysis
Pregnancy
Reverse Transcriptase Polymerase Chain Reaction
Uterus
title_short Uterine NK Cells Are Critical in Shaping DC Immunogenic Functions Compatible with Pregnancy Progression
title_full Uterine NK Cells Are Critical in Shaping DC Immunogenic Functions Compatible with Pregnancy Progression
title_fullStr Uterine NK Cells Are Critical in Shaping DC Immunogenic Functions Compatible with Pregnancy Progression
title_full_unstemmed Uterine NK Cells Are Critical in Shaping DC Immunogenic Functions Compatible with Pregnancy Progression
title_sort Uterine NK Cells Are Critical in Shaping DC Immunogenic Functions Compatible with Pregnancy Progression
dc.creator.none.fl_str_mv González, I.T.
Barrientos, G.
Freitag, N.
Otto, T.
Thijssen, V.L.J.L.
Moschansky, P.
von Kwiatkowski, P.
Klapp, B.F.
Winterhager, E.
Bauersachs, S.
Blois, S.M.
author González, I.T.
author_facet González, I.T.
Barrientos, G.
Freitag, N.
Otto, T.
Thijssen, V.L.J.L.
Moschansky, P.
von Kwiatkowski, P.
Klapp, B.F.
Winterhager, E.
Bauersachs, S.
Blois, S.M.
author_role author
author2 Barrientos, G.
Freitag, N.
Otto, T.
Thijssen, V.L.J.L.
Moschansky, P.
von Kwiatkowski, P.
Klapp, B.F.
Winterhager, E.
Bauersachs, S.
Blois, S.M.
author2_role author
author
author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv angiopoietin 1
glycoprotein p 15095
animal cell
animal tissue
article
cell differentiation
cell expansion
cell interaction
cell proliferation
cell shape
controlled study
decidualization
dendritic cell
female
first trimester pregnancy
flow cytometry
fluorescence activated cell sorting
gene expression
histopathology
immunogenicity
immunohistochemistry
inflammation
mouse
natural killer cell
nidation
nonhuman
pregnancy
pregnancy disorder
quantitative analysis
reverse transcription polymerase chain reaction
stroma cell
T cell depletion
uterine cervix
Animals
Dendritic Cells
Enzyme-Linked Immunosorbent Assay
Female
Immunohistochemistry
Killer Cells, Natural
Male
Mice
Oligonucleotide Array Sequence Analysis
Pregnancy
Reverse Transcriptase Polymerase Chain Reaction
Uterus
topic angiopoietin 1
glycoprotein p 15095
animal cell
animal tissue
article
cell differentiation
cell expansion
cell interaction
cell proliferation
cell shape
controlled study
decidualization
dendritic cell
female
first trimester pregnancy
flow cytometry
fluorescence activated cell sorting
gene expression
histopathology
immunogenicity
immunohistochemistry
inflammation
mouse
natural killer cell
nidation
nonhuman
pregnancy
pregnancy disorder
quantitative analysis
reverse transcription polymerase chain reaction
stroma cell
T cell depletion
uterine cervix
Animals
Dendritic Cells
Enzyme-Linked Immunosorbent Assay
Female
Immunohistochemistry
Killer Cells, Natural
Male
Mice
Oligonucleotide Array Sequence Analysis
Pregnancy
Reverse Transcriptase Polymerase Chain Reaction
Uterus
dc.description.none.fl_txt_mv Dendritic cell (DC) and natural killer (NK) cell interactions are important for the regulation of innate and adaptive immunity, but their relevance during early pregnancy remains elusive. Using two different strategies to manipulate the frequency of NK cells and DC during gestation, we investigated their relative impact on the decidualization process and on angiogenic responses that characterize murine implantation. Manipulation of the frequency of NK cells, DC or both lead to a defective decidual response characterized by decreased proliferation and differentiation of stromal cells. Whereas no detrimental effects were evident upon expansion of DC, NK cell ablation in such expanded DC mice severely compromised decidual development and led to early pregnancy loss. Pregnancy failure in these mice was associated with an unbalanced production of anti-angiogenic signals and most notably, with increased expression of genes related to inflammation and immunogenic activation of DC. Thus, NK cells appear to play an important role counteracting potential anomalies raised by DC expansion and overactivity in the decidua, becoming critical for normal pregnancy progression. © 2012 González et al.
description Dendritic cell (DC) and natural killer (NK) cell interactions are important for the regulation of innate and adaptive immunity, but their relevance during early pregnancy remains elusive. Using two different strategies to manipulate the frequency of NK cells and DC during gestation, we investigated their relative impact on the decidualization process and on angiogenic responses that characterize murine implantation. Manipulation of the frequency of NK cells, DC or both lead to a defective decidual response characterized by decreased proliferation and differentiation of stromal cells. Whereas no detrimental effects were evident upon expansion of DC, NK cell ablation in such expanded DC mice severely compromised decidual development and led to early pregnancy loss. Pregnancy failure in these mice was associated with an unbalanced production of anti-angiogenic signals and most notably, with increased expression of genes related to inflammation and immunogenic activation of DC. Thus, NK cells appear to play an important role counteracting potential anomalies raised by DC expansion and overactivity in the decidua, becoming critical for normal pregnancy progression. © 2012 González et al.
publishDate 2012
dc.date.none.fl_str_mv 2012
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_19326203_v7_n10_p_Gonzalez
url http://hdl.handle.net/20.500.12110/paper_19326203_v7_n10_p_Gonzalez
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 PLoS ONE 2012;7(10)
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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