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Unliganded Estrogen Receptor Alpha Promotes PC12 Survival during Serum Starvation

Many studies have reported proliferative, differentiating or protective effects of estradiol, notably through estrogen receptor alpha (ERα). On the contrary, the ligand-independent action of ERα is currently poorly documented notably in cell protection. The stable transfection of wild type, substitu...

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Autores principales: Ferriere, François, Habauzit, Denis, Pakdel, Farzad, Saligaut, Christian, Flouriot, Gilles
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3692477/
https://www.ncbi.nlm.nih.gov/pubmed/23825704
http://dx.doi.org/10.1371/journal.pone.0069081
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author Ferriere, François
Habauzit, Denis
Pakdel, Farzad
Saligaut, Christian
Flouriot, Gilles
author_facet Ferriere, François
Habauzit, Denis
Pakdel, Farzad
Saligaut, Christian
Flouriot, Gilles
author_sort Ferriere, François
collection PubMed
description Many studies have reported proliferative, differentiating or protective effects of estradiol, notably through estrogen receptor alpha (ERα). On the contrary, the ligand-independent action of ERα is currently poorly documented notably in cell protection. The stable transfection of wild type, substituted or truncated form of ERα in PC12 cells (ERα negative cell line) lead the specific study of its ligand-independent action. Hence, we demonstrate here that, in the absence of E(2), the expression of ERα prevents cells from apoptosis induced by serum deprivation. This protection is not due to an ERE-mediated transcription and does not require either AF-1 or AF-2 transactivation functions. It is afforded to the Y537 residue of ERα and activation of c-Src/Stat3 signaling pathway.
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spelling pubmed-36924772013-07-02 Unliganded Estrogen Receptor Alpha Promotes PC12 Survival during Serum Starvation Ferriere, François Habauzit, Denis Pakdel, Farzad Saligaut, Christian Flouriot, Gilles PLoS One Research Article Many studies have reported proliferative, differentiating or protective effects of estradiol, notably through estrogen receptor alpha (ERα). On the contrary, the ligand-independent action of ERα is currently poorly documented notably in cell protection. The stable transfection of wild type, substituted or truncated form of ERα in PC12 cells (ERα negative cell line) lead the specific study of its ligand-independent action. Hence, we demonstrate here that, in the absence of E(2), the expression of ERα prevents cells from apoptosis induced by serum deprivation. This protection is not due to an ERE-mediated transcription and does not require either AF-1 or AF-2 transactivation functions. It is afforded to the Y537 residue of ERα and activation of c-Src/Stat3 signaling pathway. Public Library of Science 2013-06-25 /pmc/articles/PMC3692477/ /pubmed/23825704 http://dx.doi.org/10.1371/journal.pone.0069081 Text en © 2013 Ferriere et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Ferriere, François
Habauzit, Denis
Pakdel, Farzad
Saligaut, Christian
Flouriot, Gilles
Unliganded Estrogen Receptor Alpha Promotes PC12 Survival during Serum Starvation
title Unliganded Estrogen Receptor Alpha Promotes PC12 Survival during Serum Starvation
title_full Unliganded Estrogen Receptor Alpha Promotes PC12 Survival during Serum Starvation
title_fullStr Unliganded Estrogen Receptor Alpha Promotes PC12 Survival during Serum Starvation
title_full_unstemmed Unliganded Estrogen Receptor Alpha Promotes PC12 Survival during Serum Starvation
title_short Unliganded Estrogen Receptor Alpha Promotes PC12 Survival during Serum Starvation
title_sort unliganded estrogen receptor alpha promotes pc12 survival during serum starvation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3692477/
https://www.ncbi.nlm.nih.gov/pubmed/23825704
http://dx.doi.org/10.1371/journal.pone.0069081
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