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Endogenous and Exogenous Modulation of Nrf2 Mediated Oxidative Stress Response in Bovine Granulosa Cells: Potential Implication for Ovarian Function

Nrf2 is a redox sensitive transcription factor regulating the expression of antioxidant genes as defense mechanism against various stressors. The aim of this study is to investigate the potential role of noncoding miRNAs as endogenous and quercetin as exogenous regulators of Nrf2 pathway in bovine g...

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Autores principales: Khadrawy, Omar, Gebremedhn, Samuel, Salilew-Wondim, Dessie, Taqi, Mohamed Omar, Neuhoff, Christiane, Tholen, Ernst, Hoelker, Michael, Schellander, Karl, Tesfaye, Dawit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6480527/
https://www.ncbi.nlm.nih.gov/pubmed/30986945
http://dx.doi.org/10.3390/ijms20071635
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author Khadrawy, Omar
Gebremedhn, Samuel
Salilew-Wondim, Dessie
Taqi, Mohamed Omar
Neuhoff, Christiane
Tholen, Ernst
Hoelker, Michael
Schellander, Karl
Tesfaye, Dawit
author_facet Khadrawy, Omar
Gebremedhn, Samuel
Salilew-Wondim, Dessie
Taqi, Mohamed Omar
Neuhoff, Christiane
Tholen, Ernst
Hoelker, Michael
Schellander, Karl
Tesfaye, Dawit
author_sort Khadrawy, Omar
collection PubMed
description Nrf2 is a redox sensitive transcription factor regulating the expression of antioxidant genes as defense mechanism against various stressors. The aim of this study is to investigate the potential role of noncoding miRNAs as endogenous and quercetin as exogenous regulators of Nrf2 pathway in bovine granulosa cells. For this cultured granulosa cells were used for modulation of miRNAs (miR-28, 153 and miR-708) targeting the bovine Nrf2 and supplementation of quercentin to investigate the regulatory mechanisms of the Nrf2 antioxidant system. Moreover, cultured cells were treated with hydrogen peroxide to induce oxidative stress in those cells. Our results showed that, oxidative stress activated the expression of Nrf2 as a defense mechanism, while suppressing the expression of those miRNAs. Overexpression of those miRNAs resulted in downregulation of Nrf2 expression resulted in higher ROS accumulation, reduced mitochondrial activity and cellular proliferation. Quercetin supplementation showed its protective role against oxidative stress induced by H(2)O(2) by inducing the expression of antioxidant enzymes. In conclusion, this study highlighted the involvement of miR-153, miR-28 and miR-708 in regulatory network of Nrf2 mediated antioxidant system in bovine granulosa cells function. Furthermore, quercetin at a low dose played a protective role in bovine granulosa cells against oxidative stress damage.
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spelling pubmed-64805272019-04-29 Endogenous and Exogenous Modulation of Nrf2 Mediated Oxidative Stress Response in Bovine Granulosa Cells: Potential Implication for Ovarian Function Khadrawy, Omar Gebremedhn, Samuel Salilew-Wondim, Dessie Taqi, Mohamed Omar Neuhoff, Christiane Tholen, Ernst Hoelker, Michael Schellander, Karl Tesfaye, Dawit Int J Mol Sci Article Nrf2 is a redox sensitive transcription factor regulating the expression of antioxidant genes as defense mechanism against various stressors. The aim of this study is to investigate the potential role of noncoding miRNAs as endogenous and quercetin as exogenous regulators of Nrf2 pathway in bovine granulosa cells. For this cultured granulosa cells were used for modulation of miRNAs (miR-28, 153 and miR-708) targeting the bovine Nrf2 and supplementation of quercentin to investigate the regulatory mechanisms of the Nrf2 antioxidant system. Moreover, cultured cells were treated with hydrogen peroxide to induce oxidative stress in those cells. Our results showed that, oxidative stress activated the expression of Nrf2 as a defense mechanism, while suppressing the expression of those miRNAs. Overexpression of those miRNAs resulted in downregulation of Nrf2 expression resulted in higher ROS accumulation, reduced mitochondrial activity and cellular proliferation. Quercetin supplementation showed its protective role against oxidative stress induced by H(2)O(2) by inducing the expression of antioxidant enzymes. In conclusion, this study highlighted the involvement of miR-153, miR-28 and miR-708 in regulatory network of Nrf2 mediated antioxidant system in bovine granulosa cells function. Furthermore, quercetin at a low dose played a protective role in bovine granulosa cells against oxidative stress damage. MDPI 2019-04-02 /pmc/articles/PMC6480527/ /pubmed/30986945 http://dx.doi.org/10.3390/ijms20071635 Text en © 2019 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
Khadrawy, Omar
Gebremedhn, Samuel
Salilew-Wondim, Dessie
Taqi, Mohamed Omar
Neuhoff, Christiane
Tholen, Ernst
Hoelker, Michael
Schellander, Karl
Tesfaye, Dawit
Endogenous and Exogenous Modulation of Nrf2 Mediated Oxidative Stress Response in Bovine Granulosa Cells: Potential Implication for Ovarian Function
title Endogenous and Exogenous Modulation of Nrf2 Mediated Oxidative Stress Response in Bovine Granulosa Cells: Potential Implication for Ovarian Function
title_full Endogenous and Exogenous Modulation of Nrf2 Mediated Oxidative Stress Response in Bovine Granulosa Cells: Potential Implication for Ovarian Function
title_fullStr Endogenous and Exogenous Modulation of Nrf2 Mediated Oxidative Stress Response in Bovine Granulosa Cells: Potential Implication for Ovarian Function
title_full_unstemmed Endogenous and Exogenous Modulation of Nrf2 Mediated Oxidative Stress Response in Bovine Granulosa Cells: Potential Implication for Ovarian Function
title_short Endogenous and Exogenous Modulation of Nrf2 Mediated Oxidative Stress Response in Bovine Granulosa Cells: Potential Implication for Ovarian Function
title_sort endogenous and exogenous modulation of nrf2 mediated oxidative stress response in bovine granulosa cells: potential implication for ovarian function
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6480527/
https://www.ncbi.nlm.nih.gov/pubmed/30986945
http://dx.doi.org/10.3390/ijms20071635
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