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Alpha-Lipoic Acid Plays a Role in Endometriosis: New Evidence on Inflammasome-Mediated Interleukin Production, Cellular Adhesion and Invasion

Endometriosis is an estrogen-linked gynecological disease defined by the presence of endometrial tissue on extrauterine sites where it forms invasive lesions. Alterations in estrogen-mediated cellular signaling seems to have an essential role in the pathogenesis of endometriosis. Higher estrogen rec...

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Autores principales: Di Nicuolo, Fiorella, Castellani, Roberta, De Cicco Nardone, Alessandra, Barbaro, Greta, Paciullo, Carmela, Pontecorvi, Alfredo, Scambia, Giovanni, Di Simone, Nicoletta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7826935/
https://www.ncbi.nlm.nih.gov/pubmed/33430114
http://dx.doi.org/10.3390/molecules26020288
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author Di Nicuolo, Fiorella
Castellani, Roberta
De Cicco Nardone, Alessandra
Barbaro, Greta
Paciullo, Carmela
Pontecorvi, Alfredo
Scambia, Giovanni
Di Simone, Nicoletta
author_facet Di Nicuolo, Fiorella
Castellani, Roberta
De Cicco Nardone, Alessandra
Barbaro, Greta
Paciullo, Carmela
Pontecorvi, Alfredo
Scambia, Giovanni
Di Simone, Nicoletta
author_sort Di Nicuolo, Fiorella
collection PubMed
description Endometriosis is an estrogen-linked gynecological disease defined by the presence of endometrial tissue on extrauterine sites where it forms invasive lesions. Alterations in estrogen-mediated cellular signaling seems to have an essential role in the pathogenesis of endometriosis. Higher estrogen receptor (ER)-β levels and enhanced ER-β activity were detected in endometriotic tissues. It is well known that ER-β interacts with components of the cytoplasmic inflammasome-3 (NALP-3), the NALP-3 activation increases interleukin (IL)-1β and IL-18, enhancing cellular adhesion and proliferation. Otherwise, the inhibition of ER-β activity suppresses the ectopic lesions growth. The present study aims to investigate the potential effect of α-lipoic acid (ALA) on NALP-3 and ER-β expression using a western blot analysis, NALP-3-induced cytokines production by ELISA, migration and invasion of immortalized epithelial (12Z) and stromal endometriotic cells (22B) using a 3D culture invasion assay, and matrix-metalloprotease (MMPs) activity using gelatin zymography. ALA significantly reduces ER-β, NALP-3 protein expression/activity and the secretion of IL-1β and IL-18 in both 12Z and 22B cells. ALA treatment reduces cellular adhesion and invasion via a lower expression of adhesion molecules and MMPs activities. These results provide convincing evidence that ALA might inhibit endometriosis progression.
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spelling pubmed-78269352021-01-25 Alpha-Lipoic Acid Plays a Role in Endometriosis: New Evidence on Inflammasome-Mediated Interleukin Production, Cellular Adhesion and Invasion Di Nicuolo, Fiorella Castellani, Roberta De Cicco Nardone, Alessandra Barbaro, Greta Paciullo, Carmela Pontecorvi, Alfredo Scambia, Giovanni Di Simone, Nicoletta Molecules Article Endometriosis is an estrogen-linked gynecological disease defined by the presence of endometrial tissue on extrauterine sites where it forms invasive lesions. Alterations in estrogen-mediated cellular signaling seems to have an essential role in the pathogenesis of endometriosis. Higher estrogen receptor (ER)-β levels and enhanced ER-β activity were detected in endometriotic tissues. It is well known that ER-β interacts with components of the cytoplasmic inflammasome-3 (NALP-3), the NALP-3 activation increases interleukin (IL)-1β and IL-18, enhancing cellular adhesion and proliferation. Otherwise, the inhibition of ER-β activity suppresses the ectopic lesions growth. The present study aims to investigate the potential effect of α-lipoic acid (ALA) on NALP-3 and ER-β expression using a western blot analysis, NALP-3-induced cytokines production by ELISA, migration and invasion of immortalized epithelial (12Z) and stromal endometriotic cells (22B) using a 3D culture invasion assay, and matrix-metalloprotease (MMPs) activity using gelatin zymography. ALA significantly reduces ER-β, NALP-3 protein expression/activity and the secretion of IL-1β and IL-18 in both 12Z and 22B cells. ALA treatment reduces cellular adhesion and invasion via a lower expression of adhesion molecules and MMPs activities. These results provide convincing evidence that ALA might inhibit endometriosis progression. MDPI 2021-01-08 /pmc/articles/PMC7826935/ /pubmed/33430114 http://dx.doi.org/10.3390/molecules26020288 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Di Nicuolo, Fiorella
Castellani, Roberta
De Cicco Nardone, Alessandra
Barbaro, Greta
Paciullo, Carmela
Pontecorvi, Alfredo
Scambia, Giovanni
Di Simone, Nicoletta
Alpha-Lipoic Acid Plays a Role in Endometriosis: New Evidence on Inflammasome-Mediated Interleukin Production, Cellular Adhesion and Invasion
title Alpha-Lipoic Acid Plays a Role in Endometriosis: New Evidence on Inflammasome-Mediated Interleukin Production, Cellular Adhesion and Invasion
title_full Alpha-Lipoic Acid Plays a Role in Endometriosis: New Evidence on Inflammasome-Mediated Interleukin Production, Cellular Adhesion and Invasion
title_fullStr Alpha-Lipoic Acid Plays a Role in Endometriosis: New Evidence on Inflammasome-Mediated Interleukin Production, Cellular Adhesion and Invasion
title_full_unstemmed Alpha-Lipoic Acid Plays a Role in Endometriosis: New Evidence on Inflammasome-Mediated Interleukin Production, Cellular Adhesion and Invasion
title_short Alpha-Lipoic Acid Plays a Role in Endometriosis: New Evidence on Inflammasome-Mediated Interleukin Production, Cellular Adhesion and Invasion
title_sort alpha-lipoic acid plays a role in endometriosis: new evidence on inflammasome-mediated interleukin production, cellular adhesion and invasion
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7826935/
https://www.ncbi.nlm.nih.gov/pubmed/33430114
http://dx.doi.org/10.3390/molecules26020288
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