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
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/143206
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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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1844613150942429184 |
score |
13.070432 |