Human Chorionic Gonadotropin modulates CXCL10 Expression through Histone Methylation in human decidua

Autores
Silasi, Michelle; You, Yuan; Simpson, Samantha; Kaislasuo, Janina; Pal, Lubna; Guller, Seth; Peng, Gang; Ramhorst, Rosanna Elizabeth; Grasso, Esteban Nicolas; Etemad, Shervin; Durosier, Sandy; Aldo, Paulomi; Mor, Gil
Año de publicación
2020
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The process of implantation, trophoblast invasion and placentation demand continuous adaptation and modifications between the trophoblast (embryonic) and the decidua (maternal). Within the decidua, the maternal immune system undergoes continued changes, as the pregnancy progress, in terms of the cell population, phenotype and production of immune factors, cytokines and chemokines. Human chorionic gonadotropin (hCG) is one of the earliest hormones produced by the blastocyst and has potent immune modulatory effects, especially in relation to T cells. We hypothesized that trophoblast-derived hCG modulates the immune population present at the maternal fetal interface by modifying the cytokine profile produced by the stromal/decidual cells. Using in vitro models from decidual samples we demonstrate that hCG inhibits CXCL10 expression by inducing H3K27me3 histone methylation, which binds to Region 4 of the CXCL10 promoter, thereby suppressing its expression. hCG-induced histone methylation is mediated through EZH2, a functional member of the PRC2 complex. Regulation of CXCL10 expression has a major impact on the capacity of endometrial stromal cells to recruit CD8 cells. We demonstrate the existence of a cross talk between the placenta (hCG) and the decidua (CXCL10) in the control of immune cell recruitment. Alterations in this immune regulatory function, such as during infection, will have detrimental effects on the success of the pregnancy.
Fil: Silasi, Michelle. University Of Yale. School Of Medicine. Departament Of Obstretics And Gynecology; Estados Unidos
Fil: You, Yuan. University of Yale; Estados Unidos. Wayne State University (wayne State University);
Fil: Simpson, Samantha. University of Yale; Estados Unidos
Fil: Kaislasuo, Janina. University of Yale; Estados Unidos. University of Helsinki; Finlandia
Fil: Pal, Lubna. University of Yale; Estados Unidos
Fil: Guller, Seth. University of Yale; Estados Unidos
Fil: Peng, Gang. University of Yale; Estados Unidos
Fil: Ramhorst, Rosanna Elizabeth. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química Biológica de la Facultad de Ciencias Exactas y Naturales. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química Biológica de la Facultad de Ciencias Exactas y Naturales; Argentina
Fil: Grasso, Esteban Nicolas. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química Biológica de la Facultad de Ciencias Exactas y Naturales. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química Biológica de la Facultad de Ciencias Exactas y Naturales; Argentina
Fil: Etemad, Shervin. University of Yale; Estados Unidos
Fil: Durosier, Sandy. University of Yale; Estados Unidos
Fil: Aldo, Paulomi. University of Yale; Estados Unidos
Fil: Mor, Gil. University of Yale; Estados Unidos. Wayne State University (wayne State University);
Materia
receptividad endometrial
decidualization
chemokines
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/143206

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repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling Human Chorionic Gonadotropin modulates CXCL10 Expression through Histone Methylation in human deciduaSilasi, MichelleYou, YuanSimpson, SamanthaKaislasuo, JaninaPal, LubnaGuller, SethPeng, GangRamhorst, Rosanna ElizabethGrasso, Esteban NicolasEtemad, ShervinDurosier, SandyAldo, PaulomiMor, Gilreceptividad endometrialdecidualizationchemokineshttps://purl.org/becyt/ford/3.1https://purl.org/becyt/ford/3The process of implantation, trophoblast invasion and placentation demand continuous adaptation and modifications between the trophoblast (embryonic) and the decidua (maternal). Within the decidua, the maternal immune system undergoes continued changes, as the pregnancy progress, in terms of the cell population, phenotype and production of immune factors, cytokines and chemokines. Human chorionic gonadotropin (hCG) is one of the earliest hormones produced by the blastocyst and has potent immune modulatory effects, especially in relation to T cells. We hypothesized that trophoblast-derived hCG modulates the immune population present at the maternal fetal interface by modifying the cytokine profile produced by the stromal/decidual cells. Using in vitro models from decidual samples we demonstrate that hCG inhibits CXCL10 expression by inducing H3K27me3 histone methylation, which binds to Region 4 of the CXCL10 promoter, thereby suppressing its expression. hCG-induced histone methylation is mediated through EZH2, a functional member of the PRC2 complex. Regulation of CXCL10 expression has a major impact on the capacity of endometrial stromal cells to recruit CD8 cells. We demonstrate the existence of a cross talk between the placenta (hCG) and the decidua (CXCL10) in the control of immune cell recruitment. Alterations in this immune regulatory function, such as during infection, will have detrimental effects on the success of the pregnancy.Fil: Silasi, Michelle. University Of Yale. School Of Medicine. Departament Of Obstretics And Gynecology; Estados UnidosFil: You, Yuan. University of Yale; Estados Unidos. Wayne State University (wayne State University);Fil: Simpson, Samantha. University of Yale; Estados UnidosFil: Kaislasuo, Janina. University of Yale; Estados Unidos. University of Helsinki; FinlandiaFil: Pal, Lubna. University of Yale; Estados UnidosFil: Guller, Seth. University of Yale; Estados UnidosFil: Peng, Gang. University of Yale; Estados UnidosFil: Ramhorst, Rosanna Elizabeth. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química Biológica de la Facultad de Ciencias Exactas y Naturales. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química Biológica de la Facultad de Ciencias Exactas y Naturales; ArgentinaFil: Grasso, Esteban Nicolas. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química Biológica de la Facultad de Ciencias Exactas y Naturales. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química Biológica de la Facultad de Ciencias Exactas y Naturales; ArgentinaFil: Etemad, Shervin. University of Yale; Estados UnidosFil: Durosier, Sandy. University of Yale; Estados UnidosFil: Aldo, Paulomi. University of Yale; Estados UnidosFil: Mor, Gil. University of Yale; Estados Unidos. Wayne State University (wayne State University);Nature Publishing Group2020-04-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/143206Silasi, Michelle; You, Yuan; Simpson, Samantha; Kaislasuo, Janina; Pal, Lubna; et al.; Human Chorionic Gonadotropin modulates CXCL10 Expression through Histone Methylation in human decidua; Nature Publishing Group; Scientific Reports; 10; 5785; 1-4-2020; 1-172045-2322CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/http://www.nature.com/articles/s41598-020-62593-9info:eu-repo/semantics/altIdentifier/doi/10.1038/s41598-020-62593-9info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T09:36:38Zoai:ri.conicet.gov.ar:11336/143206instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-29 09:36:38.65CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Human Chorionic Gonadotropin modulates CXCL10 Expression through Histone Methylation in human decidua
title Human Chorionic Gonadotropin modulates CXCL10 Expression through Histone Methylation in human decidua
spellingShingle Human Chorionic Gonadotropin modulates CXCL10 Expression through Histone Methylation in human decidua
Silasi, Michelle
receptividad endometrial
decidualization
chemokines
title_short Human Chorionic Gonadotropin modulates CXCL10 Expression through Histone Methylation in human decidua
title_full Human Chorionic Gonadotropin modulates CXCL10 Expression through Histone Methylation in human decidua
title_fullStr Human Chorionic Gonadotropin modulates CXCL10 Expression through Histone Methylation in human decidua
title_full_unstemmed Human Chorionic Gonadotropin modulates CXCL10 Expression through Histone Methylation in human decidua
title_sort Human Chorionic Gonadotropin modulates CXCL10 Expression through Histone Methylation in human decidua
dc.creator.none.fl_str_mv Silasi, Michelle
You, Yuan
Simpson, Samantha
Kaislasuo, Janina
Pal, Lubna
Guller, Seth
Peng, Gang
Ramhorst, Rosanna Elizabeth
Grasso, Esteban Nicolas
Etemad, Shervin
Durosier, Sandy
Aldo, Paulomi
Mor, Gil
author Silasi, Michelle
author_facet Silasi, Michelle
You, Yuan
Simpson, Samantha
Kaislasuo, Janina
Pal, Lubna
Guller, Seth
Peng, Gang
Ramhorst, Rosanna Elizabeth
Grasso, Esteban Nicolas
Etemad, Shervin
Durosier, Sandy
Aldo, Paulomi
Mor, Gil
author_role author
author2 You, Yuan
Simpson, Samantha
Kaislasuo, Janina
Pal, Lubna
Guller, Seth
Peng, Gang
Ramhorst, Rosanna Elizabeth
Grasso, Esteban Nicolas
Etemad, Shervin
Durosier, Sandy
Aldo, Paulomi
Mor, Gil
author2_role author
author
author
author
author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv receptividad endometrial
decidualization
chemokines
topic receptividad endometrial
decidualization
chemokines
purl_subject.fl_str_mv https://purl.org/becyt/ford/3.1
https://purl.org/becyt/ford/3
dc.description.none.fl_txt_mv The process of implantation, trophoblast invasion and placentation demand continuous adaptation and modifications between the trophoblast (embryonic) and the decidua (maternal). Within the decidua, the maternal immune system undergoes continued changes, as the pregnancy progress, in terms of the cell population, phenotype and production of immune factors, cytokines and chemokines. Human chorionic gonadotropin (hCG) is one of the earliest hormones produced by the blastocyst and has potent immune modulatory effects, especially in relation to T cells. We hypothesized that trophoblast-derived hCG modulates the immune population present at the maternal fetal interface by modifying the cytokine profile produced by the stromal/decidual cells. Using in vitro models from decidual samples we demonstrate that hCG inhibits CXCL10 expression by inducing H3K27me3 histone methylation, which binds to Region 4 of the CXCL10 promoter, thereby suppressing its expression. hCG-induced histone methylation is mediated through EZH2, a functional member of the PRC2 complex. Regulation of CXCL10 expression has a major impact on the capacity of endometrial stromal cells to recruit CD8 cells. We demonstrate the existence of a cross talk between the placenta (hCG) and the decidua (CXCL10) in the control of immune cell recruitment. Alterations in this immune regulatory function, such as during infection, will have detrimental effects on the success of the pregnancy.
Fil: Silasi, Michelle. University Of Yale. School Of Medicine. Departament Of Obstretics And Gynecology; Estados Unidos
Fil: You, Yuan. University of Yale; Estados Unidos. Wayne State University (wayne State University);
Fil: Simpson, Samantha. University of Yale; Estados Unidos
Fil: Kaislasuo, Janina. University of Yale; Estados Unidos. University of Helsinki; Finlandia
Fil: Pal, Lubna. University of Yale; Estados Unidos
Fil: Guller, Seth. University of Yale; Estados Unidos
Fil: Peng, Gang. University of Yale; Estados Unidos
Fil: Ramhorst, Rosanna Elizabeth. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química Biológica de la Facultad de Ciencias Exactas y Naturales. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química Biológica de la Facultad de Ciencias Exactas y Naturales; Argentina
Fil: Grasso, Esteban Nicolas. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química Biológica de la Facultad de Ciencias Exactas y Naturales. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química Biológica de la Facultad de Ciencias Exactas y Naturales; Argentina
Fil: Etemad, Shervin. University of Yale; Estados Unidos
Fil: Durosier, Sandy. University of Yale; Estados Unidos
Fil: Aldo, Paulomi. University of Yale; Estados Unidos
Fil: Mor, Gil. University of Yale; Estados Unidos. Wayne State University (wayne State University);
description The process of implantation, trophoblast invasion and placentation demand continuous adaptation and modifications between the trophoblast (embryonic) and the decidua (maternal). Within the decidua, the maternal immune system undergoes continued changes, as the pregnancy progress, in terms of the cell population, phenotype and production of immune factors, cytokines and chemokines. Human chorionic gonadotropin (hCG) is one of the earliest hormones produced by the blastocyst and has potent immune modulatory effects, especially in relation to T cells. We hypothesized that trophoblast-derived hCG modulates the immune population present at the maternal fetal interface by modifying the cytokine profile produced by the stromal/decidual cells. Using in vitro models from decidual samples we demonstrate that hCG inhibits CXCL10 expression by inducing H3K27me3 histone methylation, which binds to Region 4 of the CXCL10 promoter, thereby suppressing its expression. hCG-induced histone methylation is mediated through EZH2, a functional member of the PRC2 complex. Regulation of CXCL10 expression has a major impact on the capacity of endometrial stromal cells to recruit CD8 cells. We demonstrate the existence of a cross talk between the placenta (hCG) and the decidua (CXCL10) in the control of immune cell recruitment. Alterations in this immune regulatory function, such as during infection, will have detrimental effects on the success of the pregnancy.
publishDate 2020
dc.date.none.fl_str_mv 2020-04-01
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/11336/143206
Silasi, Michelle; You, Yuan; Simpson, Samantha; Kaislasuo, Janina; Pal, Lubna; et al.; Human Chorionic Gonadotropin modulates CXCL10 Expression through Histone Methylation in human decidua; Nature Publishing Group; Scientific Reports; 10; 5785; 1-4-2020; 1-17
2045-2322
CONICET Digital
CONICET
url http://hdl.handle.net/11336/143206
identifier_str_mv Silasi, Michelle; You, Yuan; Simpson, Samantha; Kaislasuo, Janina; Pal, Lubna; et al.; Human Chorionic Gonadotropin modulates CXCL10 Expression through Histone Methylation in human decidua; Nature Publishing Group; Scientific Reports; 10; 5785; 1-4-2020; 1-17
2045-2322
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/http://www.nature.com/articles/s41598-020-62593-9
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41598-020-62593-9
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Nature Publishing Group
publisher.none.fl_str_mv Nature Publishing Group
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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