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The expression of cystathionine gamma-lyase is regulated by estrogen receptor alpha in human osteoblasts
Hydrogen sulfide (H(2)S), generated in the osteoblasts predominantly via cystathionine-γ-lyase (CSE), is bone protective. Previous studies suggested that the onset of bone loss due to estrogen deficiency is associated to decreased levels of H(2)S and blunted gene expression of CSE. However, there ar...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5731906/ https://www.ncbi.nlm.nih.gov/pubmed/29254196 http://dx.doi.org/10.18632/oncotarget.21514 |
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author | Lambertini, Elisabetta Penolazzi, Letizia Angelozzi, Marco Grassi, Francesco Gambari, Laura Lisignoli, Gina De Bonis, Pasquale Cavallo, Michele Piva, Roberta |
author_facet | Lambertini, Elisabetta Penolazzi, Letizia Angelozzi, Marco Grassi, Francesco Gambari, Laura Lisignoli, Gina De Bonis, Pasquale Cavallo, Michele Piva, Roberta |
author_sort | Lambertini, Elisabetta |
collection | PubMed |
description | Hydrogen sulfide (H(2)S), generated in the osteoblasts predominantly via cystathionine-γ-lyase (CSE), is bone protective. Previous studies suggested that the onset of bone loss due to estrogen deficiency is associated to decreased levels of H(2)S and blunted gene expression of CSE. However, there are still a lot of unknowns on how H(2)S levels influence bone cells function. The present study aims to explore the mechanisms by which estrogen may regulate CSE expression, in particular the role of estrogen receptor alpha (ERα) in human osteoblasts (hOBs). Vertebral lamina derived hOBs were characterized and then assessed for CSE expression by western blot analysis in the presence or absence of ERα overexpression. Bioinformatic analysis, luciferase reporter assay and ChIP assay were performed to investigate ERα recruitment and activity on hCSE gene promoter. Three putative half Estrogen Responsive Elements (EREs) were identified in the hCSE core promoter and were found to participate in the ERα – mediated positive regulation of CSE expression. All osteoblast samples responded to ERα over-expression increasing the levels of CSE protein in a comparable manner. Notably, the ERα recruitment on the regulatory regions of the CSE promoter occurred predominantly in female hOBs than in male hOBs. The obtained results suggest that CSE/H(2)S system is in relation with estrogen signaling in bone in a gender specific manner. |
format | Online Article Text |
id | pubmed-5731906 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-57319062017-12-17 The expression of cystathionine gamma-lyase is regulated by estrogen receptor alpha in human osteoblasts Lambertini, Elisabetta Penolazzi, Letizia Angelozzi, Marco Grassi, Francesco Gambari, Laura Lisignoli, Gina De Bonis, Pasquale Cavallo, Michele Piva, Roberta Oncotarget Research Paper Hydrogen sulfide (H(2)S), generated in the osteoblasts predominantly via cystathionine-γ-lyase (CSE), is bone protective. Previous studies suggested that the onset of bone loss due to estrogen deficiency is associated to decreased levels of H(2)S and blunted gene expression of CSE. However, there are still a lot of unknowns on how H(2)S levels influence bone cells function. The present study aims to explore the mechanisms by which estrogen may regulate CSE expression, in particular the role of estrogen receptor alpha (ERα) in human osteoblasts (hOBs). Vertebral lamina derived hOBs were characterized and then assessed for CSE expression by western blot analysis in the presence or absence of ERα overexpression. Bioinformatic analysis, luciferase reporter assay and ChIP assay were performed to investigate ERα recruitment and activity on hCSE gene promoter. Three putative half Estrogen Responsive Elements (EREs) were identified in the hCSE core promoter and were found to participate in the ERα – mediated positive regulation of CSE expression. All osteoblast samples responded to ERα over-expression increasing the levels of CSE protein in a comparable manner. Notably, the ERα recruitment on the regulatory regions of the CSE promoter occurred predominantly in female hOBs than in male hOBs. The obtained results suggest that CSE/H(2)S system is in relation with estrogen signaling in bone in a gender specific manner. Impact Journals LLC 2017-10-04 /pmc/articles/PMC5731906/ /pubmed/29254196 http://dx.doi.org/10.18632/oncotarget.21514 Text en Copyright: © 2017 Lambertini et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Lambertini, Elisabetta Penolazzi, Letizia Angelozzi, Marco Grassi, Francesco Gambari, Laura Lisignoli, Gina De Bonis, Pasquale Cavallo, Michele Piva, Roberta The expression of cystathionine gamma-lyase is regulated by estrogen receptor alpha in human osteoblasts |
title | The expression of cystathionine gamma-lyase is regulated by estrogen receptor alpha in human osteoblasts |
title_full | The expression of cystathionine gamma-lyase is regulated by estrogen receptor alpha in human osteoblasts |
title_fullStr | The expression of cystathionine gamma-lyase is regulated by estrogen receptor alpha in human osteoblasts |
title_full_unstemmed | The expression of cystathionine gamma-lyase is regulated by estrogen receptor alpha in human osteoblasts |
title_short | The expression of cystathionine gamma-lyase is regulated by estrogen receptor alpha in human osteoblasts |
title_sort | expression of cystathionine gamma-lyase is regulated by estrogen receptor alpha in human osteoblasts |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5731906/ https://www.ncbi.nlm.nih.gov/pubmed/29254196 http://dx.doi.org/10.18632/oncotarget.21514 |
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