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The Interface of Nuclear and Membrane Steroid Signaling
Steroid hormones bind receptors in the cell nucleus and in the cell membrane. The most widely studied class of steroid hormone receptors are the nuclear receptors, named for their function as ligand-dependent transcription factors in the cell nucleus. Nuclear receptors, such as estrogen receptor alp...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Oxford University Press
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8214340/ https://www.ncbi.nlm.nih.gov/pubmed/34038515 http://dx.doi.org/10.1210/endocr/bqab107 |
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author | Treviño, Lindsey S Gorelick, Daniel A |
author_facet | Treviño, Lindsey S Gorelick, Daniel A |
author_sort | Treviño, Lindsey S |
collection | PubMed |
description | Steroid hormones bind receptors in the cell nucleus and in the cell membrane. The most widely studied class of steroid hormone receptors are the nuclear receptors, named for their function as ligand-dependent transcription factors in the cell nucleus. Nuclear receptors, such as estrogen receptor alpha, can also be anchored to the plasma membrane, where they respond to steroids by activating signaling pathways independent of their function as transcription factors. Steroids can also bind integral membrane proteins, such as the G protein–coupled estrogen receptor. Membrane estrogen and progestin receptors have been cloned and characterized in vitro and influence the development and function of many organ systems. Membrane androgen receptors were cloned and characterized in vitro, but their function as androgen receptors in vivo is unresolved. We review the identity and function of membrane proteins that bind estrogens, progestins, and androgens. We discuss evidence that membrane glucocorticoid and mineralocorticoid receptors exist, and whether glucocorticoid and mineralocorticoid nuclear receptors act at the cell membrane. In many cases, integral membrane steroid receptors act independently of nuclear steroid receptors, even though they may share a ligand. |
format | Online Article Text |
id | pubmed-8214340 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-82143402021-06-21 The Interface of Nuclear and Membrane Steroid Signaling Treviño, Lindsey S Gorelick, Daniel A Endocrinology Mini-Reviews Steroid hormones bind receptors in the cell nucleus and in the cell membrane. The most widely studied class of steroid hormone receptors are the nuclear receptors, named for their function as ligand-dependent transcription factors in the cell nucleus. Nuclear receptors, such as estrogen receptor alpha, can also be anchored to the plasma membrane, where they respond to steroids by activating signaling pathways independent of their function as transcription factors. Steroids can also bind integral membrane proteins, such as the G protein–coupled estrogen receptor. Membrane estrogen and progestin receptors have been cloned and characterized in vitro and influence the development and function of many organ systems. Membrane androgen receptors were cloned and characterized in vitro, but their function as androgen receptors in vivo is unresolved. We review the identity and function of membrane proteins that bind estrogens, progestins, and androgens. We discuss evidence that membrane glucocorticoid and mineralocorticoid receptors exist, and whether glucocorticoid and mineralocorticoid nuclear receptors act at the cell membrane. In many cases, integral membrane steroid receptors act independently of nuclear steroid receptors, even though they may share a ligand. Oxford University Press 2021-05-26 /pmc/articles/PMC8214340/ /pubmed/34038515 http://dx.doi.org/10.1210/endocr/bqab107 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the Endocrine Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Mini-Reviews Treviño, Lindsey S Gorelick, Daniel A The Interface of Nuclear and Membrane Steroid Signaling |
title | The Interface of Nuclear and Membrane Steroid Signaling |
title_full | The Interface of Nuclear and Membrane Steroid Signaling |
title_fullStr | The Interface of Nuclear and Membrane Steroid Signaling |
title_full_unstemmed | The Interface of Nuclear and Membrane Steroid Signaling |
title_short | The Interface of Nuclear and Membrane Steroid Signaling |
title_sort | interface of nuclear and membrane steroid signaling |
topic | Mini-Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8214340/ https://www.ncbi.nlm.nih.gov/pubmed/34038515 http://dx.doi.org/10.1210/endocr/bqab107 |
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