Cellular and exosome mediated molecular defense mechanism in bovine granulosa cells exposed to oxidative stress.

Various environmental insults including diseases, heat and oxidative stress could lead to abnormal growth, functions and apoptosis in granulosa cells during ovarian follicle growth and oocyte maturation. Despite the fact that cells exposed to oxidative stress are responding transcriptionally, the po...

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Main Authors: Mohammed Saeed-Zidane, Lea Linden, Dessie Salilew-Wondim, Eva Held, Christiane Neuhoff, Ernst Tholen, Michael Hoelker, Karl Schellander, Dawit Tesfaye
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5678720?pdf=render
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spelling doaj-e18479f4c8f14f2fb592c846a79b55952020-11-25T02:27:09ZengPublic Library of Science (PLoS)PLoS ONE1932-62032017-01-011211e018756910.1371/journal.pone.0187569Cellular and exosome mediated molecular defense mechanism in bovine granulosa cells exposed to oxidative stress.Mohammed Saeed-ZidaneLea LindenDessie Salilew-WondimEva HeldChristiane NeuhoffErnst TholenMichael HoelkerKarl SchellanderDawit TesfayeVarious environmental insults including diseases, heat and oxidative stress could lead to abnormal growth, functions and apoptosis in granulosa cells during ovarian follicle growth and oocyte maturation. Despite the fact that cells exposed to oxidative stress are responding transcriptionally, the potential release of transcripts associated with oxidative stress response into extracellular space through exosomes is not yet determined. Therefore, here we aimed to investigate the effect of oxidative stress in bovine granulosa cells in vitro on the cellular and exosome mediated defense mechanisms. Bovine granulosa cells were aspirated from ovarian follicles and cultured in DMEM/F-12 Ham culture medium supplemented with 10% exosome-depleted fetal bovine serum. In the first experiment sub-confluent cells were treated with 5 μM H2O2 for 40 min to induce oxidative stress. Thereafter, cells were subjected to ROS and mitochondrial staining, cell proliferation and cell cycle assays. Furthermore, gene and protein expression analysis were performed in H2O2-challenged versus control group 24 hr post-treatment using qRT-PCR and immune blotting or immunocytochemistry assay, respectively. Moreover, exosomes were isolated from spent media using ultracentrifugation procedure, and subsequently used for RNA isolation and qRT-PCR. In the second experiment, exosomes released by granulosa cells under oxidative stress (StressExo) or those released by granulosa cells without oxidative stress (NormalExo) were co-incubated with bovine granulosa cells in vitro to proof the potential horizontal transfer of defense molecules from exosomes to granulosa cells and investigate any phenotype changes. Exposure of bovine granulosa cells to H2O2 induced the accumulation of ROS, reduced mitochondrial activity, increased expression of Nrf2 and its downstream antioxidant genes (both mRNA and protein), altered the cell cycle transitions and induced cellular apoptosis. Granulosa cells exposed to oxidative stress released exosomes enriched with mRNA of Nrf2 and candidate antioxidants. Subsequent co-incubation of StressExo with cultured granulosa cells could alter the relative abundance of cellular oxidative stress response molecules including Nrf2 and antioxidants CAT, PRDX1 and TXN1. The present study provide evidences that granulosa cells exposed to oxidative stress conditions react to stress by activating cascades of cellular antioxidant molecules which can also be released into extracellular environment through exosomes.http://europepmc.org/articles/PMC5678720?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Mohammed Saeed-Zidane
Lea Linden
Dessie Salilew-Wondim
Eva Held
Christiane Neuhoff
Ernst Tholen
Michael Hoelker
Karl Schellander
Dawit Tesfaye
spellingShingle Mohammed Saeed-Zidane
Lea Linden
Dessie Salilew-Wondim
Eva Held
Christiane Neuhoff
Ernst Tholen
Michael Hoelker
Karl Schellander
Dawit Tesfaye
Cellular and exosome mediated molecular defense mechanism in bovine granulosa cells exposed to oxidative stress.
PLoS ONE
author_facet Mohammed Saeed-Zidane
Lea Linden
Dessie Salilew-Wondim
Eva Held
Christiane Neuhoff
Ernst Tholen
Michael Hoelker
Karl Schellander
Dawit Tesfaye
author_sort Mohammed Saeed-Zidane
title Cellular and exosome mediated molecular defense mechanism in bovine granulosa cells exposed to oxidative stress.
title_short Cellular and exosome mediated molecular defense mechanism in bovine granulosa cells exposed to oxidative stress.
title_full Cellular and exosome mediated molecular defense mechanism in bovine granulosa cells exposed to oxidative stress.
title_fullStr Cellular and exosome mediated molecular defense mechanism in bovine granulosa cells exposed to oxidative stress.
title_full_unstemmed Cellular and exosome mediated molecular defense mechanism in bovine granulosa cells exposed to oxidative stress.
title_sort cellular and exosome mediated molecular defense mechanism in bovine granulosa cells exposed to oxidative stress.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2017-01-01
description Various environmental insults including diseases, heat and oxidative stress could lead to abnormal growth, functions and apoptosis in granulosa cells during ovarian follicle growth and oocyte maturation. Despite the fact that cells exposed to oxidative stress are responding transcriptionally, the potential release of transcripts associated with oxidative stress response into extracellular space through exosomes is not yet determined. Therefore, here we aimed to investigate the effect of oxidative stress in bovine granulosa cells in vitro on the cellular and exosome mediated defense mechanisms. Bovine granulosa cells were aspirated from ovarian follicles and cultured in DMEM/F-12 Ham culture medium supplemented with 10% exosome-depleted fetal bovine serum. In the first experiment sub-confluent cells were treated with 5 μM H2O2 for 40 min to induce oxidative stress. Thereafter, cells were subjected to ROS and mitochondrial staining, cell proliferation and cell cycle assays. Furthermore, gene and protein expression analysis were performed in H2O2-challenged versus control group 24 hr post-treatment using qRT-PCR and immune blotting or immunocytochemistry assay, respectively. Moreover, exosomes were isolated from spent media using ultracentrifugation procedure, and subsequently used for RNA isolation and qRT-PCR. In the second experiment, exosomes released by granulosa cells under oxidative stress (StressExo) or those released by granulosa cells without oxidative stress (NormalExo) were co-incubated with bovine granulosa cells in vitro to proof the potential horizontal transfer of defense molecules from exosomes to granulosa cells and investigate any phenotype changes. Exposure of bovine granulosa cells to H2O2 induced the accumulation of ROS, reduced mitochondrial activity, increased expression of Nrf2 and its downstream antioxidant genes (both mRNA and protein), altered the cell cycle transitions and induced cellular apoptosis. Granulosa cells exposed to oxidative stress released exosomes enriched with mRNA of Nrf2 and candidate antioxidants. Subsequent co-incubation of StressExo with cultured granulosa cells could alter the relative abundance of cellular oxidative stress response molecules including Nrf2 and antioxidants CAT, PRDX1 and TXN1. The present study provide evidences that granulosa cells exposed to oxidative stress conditions react to stress by activating cascades of cellular antioxidant molecules which can also be released into extracellular environment through exosomes.
url http://europepmc.org/articles/PMC5678720?pdf=render
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