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
- 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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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 |
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ana@bl.fcen.uba.ar |
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