Cargando…

TRIM28 modulates nuclear receptor signaling to regulate uterine function

Estrogen and progesterone, acting through their cognate receptors the estrogen receptor α (ERα) and the progesterone receptor (PR) respectively, regulate uterine biology. Using rapid immunoprecipitation and mass spectrometry (RIME) and co-immunoprecipitation, we identified TRIM28 (Tripartite motif c...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Rong, Wang, Tianyuan, Marquardt, Ryan M., Lydon, John P., Wu, San-Pin, DeMayo, Francesco J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10393996/
https://www.ncbi.nlm.nih.gov/pubmed/37528140
http://dx.doi.org/10.1038/s41467-023-40395-7
_version_ 1785083268304994304
author Li, Rong
Wang, Tianyuan
Marquardt, Ryan M.
Lydon, John P.
Wu, San-Pin
DeMayo, Francesco J.
author_facet Li, Rong
Wang, Tianyuan
Marquardt, Ryan M.
Lydon, John P.
Wu, San-Pin
DeMayo, Francesco J.
author_sort Li, Rong
collection PubMed
description Estrogen and progesterone, acting through their cognate receptors the estrogen receptor α (ERα) and the progesterone receptor (PR) respectively, regulate uterine biology. Using rapid immunoprecipitation and mass spectrometry (RIME) and co-immunoprecipitation, we identified TRIM28 (Tripartite motif containing 28) as a protein which complexes with ERα and PR in the regulation of uterine function. Impairment of TRIM28 expression results in the inability of the uterus to support early pregnancy through altered PR and ERα action in the uterine epithelium and stroma by suppressing PR and ERα chromatin binding. Furthermore, TRIM28 ablation in PR-expressing uterine cells results in the enrichment of a subset of TRIM28 positive and PR negative pericytes and epithelial cells with progenitor potential. In summary, our study reveals the important roles of TRIM28 in regulating endometrial cell composition and function in women, and also implies its critical functions in other hormone regulated systems.
format Online
Article
Text
id pubmed-10393996
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-103939962023-08-03 TRIM28 modulates nuclear receptor signaling to regulate uterine function Li, Rong Wang, Tianyuan Marquardt, Ryan M. Lydon, John P. Wu, San-Pin DeMayo, Francesco J. Nat Commun Article Estrogen and progesterone, acting through their cognate receptors the estrogen receptor α (ERα) and the progesterone receptor (PR) respectively, regulate uterine biology. Using rapid immunoprecipitation and mass spectrometry (RIME) and co-immunoprecipitation, we identified TRIM28 (Tripartite motif containing 28) as a protein which complexes with ERα and PR in the regulation of uterine function. Impairment of TRIM28 expression results in the inability of the uterus to support early pregnancy through altered PR and ERα action in the uterine epithelium and stroma by suppressing PR and ERα chromatin binding. Furthermore, TRIM28 ablation in PR-expressing uterine cells results in the enrichment of a subset of TRIM28 positive and PR negative pericytes and epithelial cells with progenitor potential. In summary, our study reveals the important roles of TRIM28 in regulating endometrial cell composition and function in women, and also implies its critical functions in other hormone regulated systems. Nature Publishing Group UK 2023-08-01 /pmc/articles/PMC10393996/ /pubmed/37528140 http://dx.doi.org/10.1038/s41467-023-40395-7 Text en © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Li, Rong
Wang, Tianyuan
Marquardt, Ryan M.
Lydon, John P.
Wu, San-Pin
DeMayo, Francesco J.
TRIM28 modulates nuclear receptor signaling to regulate uterine function
title TRIM28 modulates nuclear receptor signaling to regulate uterine function
title_full TRIM28 modulates nuclear receptor signaling to regulate uterine function
title_fullStr TRIM28 modulates nuclear receptor signaling to regulate uterine function
title_full_unstemmed TRIM28 modulates nuclear receptor signaling to regulate uterine function
title_short TRIM28 modulates nuclear receptor signaling to regulate uterine function
title_sort trim28 modulates nuclear receptor signaling to regulate uterine function
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10393996/
https://www.ncbi.nlm.nih.gov/pubmed/37528140
http://dx.doi.org/10.1038/s41467-023-40395-7
work_keys_str_mv AT lirong trim28modulatesnuclearreceptorsignalingtoregulateuterinefunction
AT wangtianyuan trim28modulatesnuclearreceptorsignalingtoregulateuterinefunction
AT marquardtryanm trim28modulatesnuclearreceptorsignalingtoregulateuterinefunction
AT lydonjohnp trim28modulatesnuclearreceptorsignalingtoregulateuterinefunction
AT wusanpin trim28modulatesnuclearreceptorsignalingtoregulateuterinefunction
AT demayofrancescoj trim28modulatesnuclearreceptorsignalingtoregulateuterinefunction