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The role of membrane ERα signaling in bone and other major estrogen responsive tissues
Estrogen receptor α (ERα) signaling leads to cellular responses in several tissues and in addition to nuclear ERα-mediated effects, membrane ERα (mERα) signaling may be of importance. To elucidate the significance, in vivo, of mERα signaling in multiple estrogen-responsive tissues, we have used fema...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4937452/ https://www.ncbi.nlm.nih.gov/pubmed/27388455 http://dx.doi.org/10.1038/srep29473 |
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author | Gustafsson, K. L. Farman, H. Henning, P. Lionikaite, V. Movérare-Skrtic, S. Wu, J. Ryberg, H. Koskela, A. Gustafsson, J.-Å. Tuukkanen, J. Levin, E. R. Ohlsson, C. Lagerquist, M. K. |
author_facet | Gustafsson, K. L. Farman, H. Henning, P. Lionikaite, V. Movérare-Skrtic, S. Wu, J. Ryberg, H. Koskela, A. Gustafsson, J.-Å. Tuukkanen, J. Levin, E. R. Ohlsson, C. Lagerquist, M. K. |
author_sort | Gustafsson, K. L. |
collection | PubMed |
description | Estrogen receptor α (ERα) signaling leads to cellular responses in several tissues and in addition to nuclear ERα-mediated effects, membrane ERα (mERα) signaling may be of importance. To elucidate the significance, in vivo, of mERα signaling in multiple estrogen-responsive tissues, we have used female mice lacking the ability to localize ERα to the membrane due to a point mutation in the palmitoylation site (C451A), so called Nuclear-Only-ER (NOER) mice. Interestingly, the role of mERα signaling for the estrogen response was highly tissue-dependent, with trabecular bone in the axial skeleton being strongly dependent (>80% reduction in estrogen response in NOER mice), cortical and trabecular bone in long bones, as well as uterus and thymus being partly dependent (40–70% reduction in estrogen response in NOER mice) and effects on liver weight and total body fat mass being essentially independent of mERα (<35% reduction in estrogen response in NOER mice). In conclusion, mERα signaling is important for the estrogenic response in female mice in a tissue-dependent manner. Increased knowledge regarding membrane initiated ERα actions may provide means to develop new selective estrogen receptor modulators with improved profiles. |
format | Online Article Text |
id | pubmed-4937452 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49374522016-07-13 The role of membrane ERα signaling in bone and other major estrogen responsive tissues Gustafsson, K. L. Farman, H. Henning, P. Lionikaite, V. Movérare-Skrtic, S. Wu, J. Ryberg, H. Koskela, A. Gustafsson, J.-Å. Tuukkanen, J. Levin, E. R. Ohlsson, C. Lagerquist, M. K. Sci Rep Article Estrogen receptor α (ERα) signaling leads to cellular responses in several tissues and in addition to nuclear ERα-mediated effects, membrane ERα (mERα) signaling may be of importance. To elucidate the significance, in vivo, of mERα signaling in multiple estrogen-responsive tissues, we have used female mice lacking the ability to localize ERα to the membrane due to a point mutation in the palmitoylation site (C451A), so called Nuclear-Only-ER (NOER) mice. Interestingly, the role of mERα signaling for the estrogen response was highly tissue-dependent, with trabecular bone in the axial skeleton being strongly dependent (>80% reduction in estrogen response in NOER mice), cortical and trabecular bone in long bones, as well as uterus and thymus being partly dependent (40–70% reduction in estrogen response in NOER mice) and effects on liver weight and total body fat mass being essentially independent of mERα (<35% reduction in estrogen response in NOER mice). In conclusion, mERα signaling is important for the estrogenic response in female mice in a tissue-dependent manner. Increased knowledge regarding membrane initiated ERα actions may provide means to develop new selective estrogen receptor modulators with improved profiles. Nature Publishing Group 2016-07-08 /pmc/articles/PMC4937452/ /pubmed/27388455 http://dx.doi.org/10.1038/srep29473 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Gustafsson, K. L. Farman, H. Henning, P. Lionikaite, V. Movérare-Skrtic, S. Wu, J. Ryberg, H. Koskela, A. Gustafsson, J.-Å. Tuukkanen, J. Levin, E. R. Ohlsson, C. Lagerquist, M. K. The role of membrane ERα signaling in bone and other major estrogen responsive tissues |
title | The role of membrane ERα signaling in bone and other major estrogen responsive tissues |
title_full | The role of membrane ERα signaling in bone and other major estrogen responsive tissues |
title_fullStr | The role of membrane ERα signaling in bone and other major estrogen responsive tissues |
title_full_unstemmed | The role of membrane ERα signaling in bone and other major estrogen responsive tissues |
title_short | The role of membrane ERα signaling in bone and other major estrogen responsive tissues |
title_sort | role of membrane erα signaling in bone and other major estrogen responsive tissues |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4937452/ https://www.ncbi.nlm.nih.gov/pubmed/27388455 http://dx.doi.org/10.1038/srep29473 |
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