Do GnRH analogues directly affect human endometrial epithelial cell gene expression?
- Autores
- Zhang, Xiaomei; Bocca, Silvina; Franchi, Nilda Anahi; Anderson, Sandra; Kaur, Mandeep; Bajic, Vladimir B.; Oehninger, Sergio
- Año de publicación
- 2010
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- We examined whether Gonadotrophin-releasing hormone (GnRH) analogues [leuprolide acetate (LA) and ganirelix acetate (GA)] modulate gene expression in Ishikawa cells used as surrogate for human endometrial epithelial cells in vitro. The specific aims were: (i) to study the modulatory effect of GnRH analogues by RT –PCR [in the absence and presence of E2 and P4, and cyclic adenosine monophosphate (cAMP)] on mRNA expression of genes modulated during the window of implantation in GnRH analogues/rFSH-treated assisted reproductive technology cycles including OPTINEURIN (OPTN), CHROMATIN MODIFYING PROTEIN (CHMP1A), PROSAPOSIN (PSAP), IGFBP-5 and SORTING NEXIN 7 (SNX7), and (ii) to analyze the 5′ -flanking regions of such genes for the presence of putative steroid-response elements [estrogen-response elements (EREs) and P4-response element (PREs)]. Ishikawa cells were cytokeratin+/vimentin2 and expressed ERa, ERb, PR and GnRH-R proteins. At 6 and 24 h, neither LA nor GA alone had an effect on gene expression. GnRH analogues alone or following E2 and/or P4 co-incubation for 24 h also had no effect on gene expression, but P4 significantly increased expression of CHMP1A. E2 + P4 treatment for 4 days, alone or followed by GA, had no effect, but E2 + P4 treatment followed by LA significantly decreased IGFBP-5 expression. The addition of 8-Br cAMP did not modify gene expression, with the exception of IGFBP-5 that was significantly increased. The GnRH analogues did not modify intracellular cAMP levels. We identified conserved EREs for OPN, CHMP1A, SNX7 and PSAP and PREs for SNX7. We conclude that GnRH analogues appear not to have major direct effects on gene expression of human endometrial epithelial cells in vitro.
Fil: Zhang, Xiaomei. Eastern Virginia Medical School; Estados Unidos
Fil: Bocca, Silvina. Eastern Virginia Medical School; Estados Unidos
Fil: Franchi, Nilda Anahi. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones Biológicas y Tecnológicas. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas, Físicas y Naturales. Instituto de Investigaciones Biológicas y Tecnológicas; Argentina
Fil: Anderson, Sandra. Eastern Virginia Medical School; Estados Unidos
Fil: Kaur, Mandeep. King Abdullah University of Science and Technology; Arabia Saudita
Fil: Bajic, Vladimir B.. King Abdullah University of Science and Technology; Arabia Saudita
Fil: Oehninger, Sergio. Eastern Virginia Medical School; Estados Unidos - Materia
-
Gene Expression
Ishikawa Cells
Endometrium
Gnrh - 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:11336/43009
Ver los metadatos del registro completo
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Do GnRH analogues directly affect human endometrial epithelial cell gene expression?Zhang, XiaomeiBocca, SilvinaFranchi, Nilda AnahiAnderson, SandraKaur, MandeepBajic, Vladimir B.Oehninger, SergioGene ExpressionIshikawa CellsEndometriumGnrhhttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1We examined whether Gonadotrophin-releasing hormone (GnRH) analogues [leuprolide acetate (LA) and ganirelix acetate (GA)] modulate gene expression in Ishikawa cells used as surrogate for human endometrial epithelial cells in vitro. The specific aims were: (i) to study the modulatory effect of GnRH analogues by RT –PCR [in the absence and presence of E2 and P4, and cyclic adenosine monophosphate (cAMP)] on mRNA expression of genes modulated during the window of implantation in GnRH analogues/rFSH-treated assisted reproductive technology cycles including OPTINEURIN (OPTN), CHROMATIN MODIFYING PROTEIN (CHMP1A), PROSAPOSIN (PSAP), IGFBP-5 and SORTING NEXIN 7 (SNX7), and (ii) to analyze the 5′ -flanking regions of such genes for the presence of putative steroid-response elements [estrogen-response elements (EREs) and P4-response element (PREs)]. Ishikawa cells were cytokeratin+/vimentin2 and expressed ERa, ERb, PR and GnRH-R proteins. At 6 and 24 h, neither LA nor GA alone had an effect on gene expression. GnRH analogues alone or following E2 and/or P4 co-incubation for 24 h also had no effect on gene expression, but P4 significantly increased expression of CHMP1A. E2 + P4 treatment for 4 days, alone or followed by GA, had no effect, but E2 + P4 treatment followed by LA significantly decreased IGFBP-5 expression. The addition of 8-Br cAMP did not modify gene expression, with the exception of IGFBP-5 that was significantly increased. The GnRH analogues did not modify intracellular cAMP levels. We identified conserved EREs for OPN, CHMP1A, SNX7 and PSAP and PREs for SNX7. We conclude that GnRH analogues appear not to have major direct effects on gene expression of human endometrial epithelial cells in vitro.Fil: Zhang, Xiaomei. Eastern Virginia Medical School; Estados UnidosFil: Bocca, Silvina. Eastern Virginia Medical School; Estados UnidosFil: Franchi, Nilda Anahi. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones Biológicas y Tecnológicas. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas, Físicas y Naturales. Instituto de Investigaciones Biológicas y Tecnológicas; ArgentinaFil: Anderson, Sandra. Eastern Virginia Medical School; Estados UnidosFil: Kaur, Mandeep. King Abdullah University of Science and Technology; Arabia SauditaFil: Bajic, Vladimir B.. King Abdullah University of Science and Technology; Arabia SauditaFil: Oehninger, Sergio. Eastern Virginia Medical School; Estados UnidosOxford University Press2010-06info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/43009Zhang, Xiaomei; Bocca, Silvina; Franchi, Nilda Anahi; Anderson, Sandra; Kaur, Mandeep; et al.; Do GnRH analogues directly affect human endometrial epithelial cell gene expression?; Oxford University Press; Molecular Human Reproduction; 16; 5; 6-2010; 347-3601360-99471460-2407CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://academic.oup.com/molehr/article/16/5/347/1060836info:eu-repo/semantics/altIdentifier/doi/10.1093/molehr/gaq012info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T09:42:15Zoai:ri.conicet.gov.ar:11336/43009instacron: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 09:42:16.13CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Do GnRH analogues directly affect human endometrial epithelial cell gene expression? |
title |
Do GnRH analogues directly affect human endometrial epithelial cell gene expression? |
spellingShingle |
Do GnRH analogues directly affect human endometrial epithelial cell gene expression? Zhang, Xiaomei Gene Expression Ishikawa Cells Endometrium Gnrh |
title_short |
Do GnRH analogues directly affect human endometrial epithelial cell gene expression? |
title_full |
Do GnRH analogues directly affect human endometrial epithelial cell gene expression? |
title_fullStr |
Do GnRH analogues directly affect human endometrial epithelial cell gene expression? |
title_full_unstemmed |
Do GnRH analogues directly affect human endometrial epithelial cell gene expression? |
title_sort |
Do GnRH analogues directly affect human endometrial epithelial cell gene expression? |
dc.creator.none.fl_str_mv |
Zhang, Xiaomei Bocca, Silvina Franchi, Nilda Anahi Anderson, Sandra Kaur, Mandeep Bajic, Vladimir B. Oehninger, Sergio |
author |
Zhang, Xiaomei |
author_facet |
Zhang, Xiaomei Bocca, Silvina Franchi, Nilda Anahi Anderson, Sandra Kaur, Mandeep Bajic, Vladimir B. Oehninger, Sergio |
author_role |
author |
author2 |
Bocca, Silvina Franchi, Nilda Anahi Anderson, Sandra Kaur, Mandeep Bajic, Vladimir B. Oehninger, Sergio |
author2_role |
author author author author author author |
dc.subject.none.fl_str_mv |
Gene Expression Ishikawa Cells Endometrium Gnrh |
topic |
Gene Expression Ishikawa Cells Endometrium Gnrh |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.6 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
We examined whether Gonadotrophin-releasing hormone (GnRH) analogues [leuprolide acetate (LA) and ganirelix acetate (GA)] modulate gene expression in Ishikawa cells used as surrogate for human endometrial epithelial cells in vitro. The specific aims were: (i) to study the modulatory effect of GnRH analogues by RT –PCR [in the absence and presence of E2 and P4, and cyclic adenosine monophosphate (cAMP)] on mRNA expression of genes modulated during the window of implantation in GnRH analogues/rFSH-treated assisted reproductive technology cycles including OPTINEURIN (OPTN), CHROMATIN MODIFYING PROTEIN (CHMP1A), PROSAPOSIN (PSAP), IGFBP-5 and SORTING NEXIN 7 (SNX7), and (ii) to analyze the 5′ -flanking regions of such genes for the presence of putative steroid-response elements [estrogen-response elements (EREs) and P4-response element (PREs)]. Ishikawa cells were cytokeratin+/vimentin2 and expressed ERa, ERb, PR and GnRH-R proteins. At 6 and 24 h, neither LA nor GA alone had an effect on gene expression. GnRH analogues alone or following E2 and/or P4 co-incubation for 24 h also had no effect on gene expression, but P4 significantly increased expression of CHMP1A. E2 + P4 treatment for 4 days, alone or followed by GA, had no effect, but E2 + P4 treatment followed by LA significantly decreased IGFBP-5 expression. The addition of 8-Br cAMP did not modify gene expression, with the exception of IGFBP-5 that was significantly increased. The GnRH analogues did not modify intracellular cAMP levels. We identified conserved EREs for OPN, CHMP1A, SNX7 and PSAP and PREs for SNX7. We conclude that GnRH analogues appear not to have major direct effects on gene expression of human endometrial epithelial cells in vitro. Fil: Zhang, Xiaomei. Eastern Virginia Medical School; Estados Unidos Fil: Bocca, Silvina. Eastern Virginia Medical School; Estados Unidos Fil: Franchi, Nilda Anahi. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones Biológicas y Tecnológicas. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas, Físicas y Naturales. Instituto de Investigaciones Biológicas y Tecnológicas; Argentina Fil: Anderson, Sandra. Eastern Virginia Medical School; Estados Unidos Fil: Kaur, Mandeep. King Abdullah University of Science and Technology; Arabia Saudita Fil: Bajic, Vladimir B.. King Abdullah University of Science and Technology; Arabia Saudita Fil: Oehninger, Sergio. Eastern Virginia Medical School; Estados Unidos |
description |
We examined whether Gonadotrophin-releasing hormone (GnRH) analogues [leuprolide acetate (LA) and ganirelix acetate (GA)] modulate gene expression in Ishikawa cells used as surrogate for human endometrial epithelial cells in vitro. The specific aims were: (i) to study the modulatory effect of GnRH analogues by RT –PCR [in the absence and presence of E2 and P4, and cyclic adenosine monophosphate (cAMP)] on mRNA expression of genes modulated during the window of implantation in GnRH analogues/rFSH-treated assisted reproductive technology cycles including OPTINEURIN (OPTN), CHROMATIN MODIFYING PROTEIN (CHMP1A), PROSAPOSIN (PSAP), IGFBP-5 and SORTING NEXIN 7 (SNX7), and (ii) to analyze the 5′ -flanking regions of such genes for the presence of putative steroid-response elements [estrogen-response elements (EREs) and P4-response element (PREs)]. Ishikawa cells were cytokeratin+/vimentin2 and expressed ERa, ERb, PR and GnRH-R proteins. At 6 and 24 h, neither LA nor GA alone had an effect on gene expression. GnRH analogues alone or following E2 and/or P4 co-incubation for 24 h also had no effect on gene expression, but P4 significantly increased expression of CHMP1A. E2 + P4 treatment for 4 days, alone or followed by GA, had no effect, but E2 + P4 treatment followed by LA significantly decreased IGFBP-5 expression. The addition of 8-Br cAMP did not modify gene expression, with the exception of IGFBP-5 that was significantly increased. The GnRH analogues did not modify intracellular cAMP levels. We identified conserved EREs for OPN, CHMP1A, SNX7 and PSAP and PREs for SNX7. We conclude that GnRH analogues appear not to have major direct effects on gene expression of human endometrial epithelial cells in vitro. |
publishDate |
2010 |
dc.date.none.fl_str_mv |
2010-06 |
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/11336/43009 Zhang, Xiaomei; Bocca, Silvina; Franchi, Nilda Anahi; Anderson, Sandra; Kaur, Mandeep; et al.; Do GnRH analogues directly affect human endometrial epithelial cell gene expression?; Oxford University Press; Molecular Human Reproduction; 16; 5; 6-2010; 347-360 1360-9947 1460-2407 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/43009 |
identifier_str_mv |
Zhang, Xiaomei; Bocca, Silvina; Franchi, Nilda Anahi; Anderson, Sandra; Kaur, Mandeep; et al.; Do GnRH analogues directly affect human endometrial epithelial cell gene expression?; Oxford University Press; Molecular Human Reproduction; 16; 5; 6-2010; 347-360 1360-9947 1460-2407 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/https://academic.oup.com/molehr/article/16/5/347/1060836 info:eu-repo/semantics/altIdentifier/doi/10.1093/molehr/gaq012 |
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 application/pdf |
dc.publisher.none.fl_str_mv |
Oxford University Press |
publisher.none.fl_str_mv |
Oxford University Press |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
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CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
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Consejo Nacional de Investigaciones Científicas y Técnicas |
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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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13.070432 |