Melatonin Modifies Histone Acetylation during In Vitro Maturation of Mouse Oocytes
Objective We evaluated the effect of melatonin, as a potent antioxidant agent, on glutathione (GSH) and reactive oxygen species (ROS) levels, as well as histone H3 lysine 9 (H3K9), and H4 lysine 12 (H4K12) acetylation when added to oocytes culture medium. Materials and Methods In this experimen...
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doaj-5d0e451439c948de9f2188405ba603b62020-11-25T01:37:47ZengRoyan Institute (ACECR), TehranCell Journal2228-58062228-58142018-04-0120224424910.22074/cellj.2018.4860Melatonin Modifies Histone Acetylation during In Vitro Maturation of Mouse Oocytes Somayeh Keshavarzi0Mohammad Salehi1Fattaneh Farifteh-Nobijari2Taher Hosseini3Sara Hosseini4Alaleh Ghazifard5Marefat Ghaffari Novin6 Vahid Fallah-Omrani7 Mohsen Nourozian8Ahmad Hosseini9Cellular and Molecular Biology Research Center, Shahid Beheshti University of Medical Sciences, Tehran, IranDepartment of Biotechnology, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, IranCellular and Molecular Biology Research Center, Shahid Beheshti University of Medical Sciences, Tehran, IranCellular and Molecular Biology Research Center, Shahid Beheshti University of Medical Sciences, Tehran, IranCellular and Molecular Biology Research Center, Shahid Beheshti University of Medical Sciences, Tehran, IranDepartment of Biology and Anatomical Sciences, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, IranDepartment of Biology and Anatomical Sciences, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, IranCellular and Molecular Biology Research Center, Shahid Beheshti University of Medical Sciences, Tehran, IranDepartment of Biology and Anatomical Sciences, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, IranCellular and Molecular Biology Research Center, Shahid Beheshti University of Medical Sciences, Tehran, IranObjective We evaluated the effect of melatonin, as a potent antioxidant agent, on glutathione (GSH) and reactive oxygen species (ROS) levels, as well as histone H3 lysine 9 (H3K9), and H4 lysine 12 (H4K12) acetylation when added to oocytes culture medium. Materials and Methods In this experimental study, two in vitro and in vivo groups were used. In the in vitro group, cumulus oocyte complexes (COCs) from the ovaries of B6D2F1 mice were cultured in maturation medium containing two doses of melatonin (10-9 and 10-6 M) and without melatonin [control group treated with dimethyl sulfoxide (DMSO)] for 22-24 hour. The cumulus expansion and nuclear status were monitored by an inverted microscope. Next, COCs were isolated from the oviducts of superovulated mice and studied as the in vivo group. In in vitro and in vivo matured oocytes, GSH and ROS levels were assessed by monochlorobimane (MCB) and 2-7-dichlorodihydrofluorescein diacetate (H2DCFDA) staining, respectively. Changes in histone acetylation were examined by immunofluorescent staining with specific antibodies against acetylated H3K9 and H4K12. Results The H4K12 acetylation and ROS levels were significantly higher in the oocytes matured in the in vitro group compared to the in vivo group (P<0.05). Furthermore, glutathione levels in the in vitro group were considerably lower than that of the in vivo group (P<0.05). Melatonin at the concentration of 10-6 M had the most substantial effect on nuclear maturation and histone acetylation as well as glutathione and ROS levels in the in vitro group (P<0.05). Conclusion Exogenous melatonin improves the competence of mouse oocytes during in vitro maturation (IVM).http://celljournal.org/journal/article/19692/downloadGlutathioneIn Vitro Oocyte MaturationMelatoninReactive Oxygen Species |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Somayeh Keshavarzi Mohammad Salehi Fattaneh Farifteh-Nobijari Taher Hosseini Sara Hosseini Alaleh Ghazifard Marefat Ghaffari Novin Vahid Fallah-Omrani Mohsen Nourozian Ahmad Hosseini |
spellingShingle |
Somayeh Keshavarzi Mohammad Salehi Fattaneh Farifteh-Nobijari Taher Hosseini Sara Hosseini Alaleh Ghazifard Marefat Ghaffari Novin Vahid Fallah-Omrani Mohsen Nourozian Ahmad Hosseini Melatonin Modifies Histone Acetylation during In Vitro Maturation of Mouse Oocytes Cell Journal Glutathione In Vitro Oocyte Maturation Melatonin Reactive Oxygen Species |
author_facet |
Somayeh Keshavarzi Mohammad Salehi Fattaneh Farifteh-Nobijari Taher Hosseini Sara Hosseini Alaleh Ghazifard Marefat Ghaffari Novin Vahid Fallah-Omrani Mohsen Nourozian Ahmad Hosseini |
author_sort |
Somayeh Keshavarzi |
title |
Melatonin Modifies Histone Acetylation during In Vitro Maturation of Mouse Oocytes |
title_short |
Melatonin Modifies Histone Acetylation during In Vitro Maturation of Mouse Oocytes |
title_full |
Melatonin Modifies Histone Acetylation during In Vitro Maturation of Mouse Oocytes |
title_fullStr |
Melatonin Modifies Histone Acetylation during In Vitro Maturation of Mouse Oocytes |
title_full_unstemmed |
Melatonin Modifies Histone Acetylation during In Vitro Maturation of Mouse Oocytes |
title_sort |
melatonin modifies histone acetylation during in vitro maturation of mouse oocytes |
publisher |
Royan Institute (ACECR), Tehran |
series |
Cell Journal |
issn |
2228-5806 2228-5814 |
publishDate |
2018-04-01 |
description |
Objective
We evaluated the effect of melatonin, as a potent antioxidant agent, on glutathione (GSH) and reactive oxygen species (ROS) levels, as well as histone H3 lysine 9 (H3K9), and H4 lysine 12 (H4K12) acetylation when added to oocytes culture medium.
Materials and Methods
In this experimental study, two in vitro and in vivo groups were used. In the in vitro group, cumulus oocyte complexes (COCs) from the ovaries of B6D2F1 mice were cultured in maturation medium containing two doses of melatonin (10-9 and 10-6 M) and without melatonin [control group treated with dimethyl sulfoxide (DMSO)] for 22-24 hour. The cumulus expansion and nuclear status were monitored by an inverted microscope. Next, COCs were isolated from the oviducts of superovulated mice and studied as the in vivo group. In in vitro and in vivo matured oocytes, GSH and ROS levels were assessed by monochlorobimane (MCB) and 2-7-dichlorodihydrofluorescein diacetate (H2DCFDA) staining, respectively. Changes in histone acetylation were examined by immunofluorescent staining with specific antibodies against acetylated H3K9 and H4K12.
Results
The H4K12 acetylation and ROS levels were significantly higher in the oocytes matured in the in vitro group compared to the in vivo group (P<0.05). Furthermore, glutathione levels in the in vitro group were considerably lower than that of the in vivo group (P<0.05). Melatonin at the concentration of 10-6 M had the most substantial effect on nuclear maturation and histone acetylation as well as glutathione and ROS levels in the in vitro group (P<0.05).
Conclusion
Exogenous melatonin improves the competence of mouse oocytes during in vitro maturation (IVM). |
topic |
Glutathione In Vitro Oocyte Maturation Melatonin Reactive Oxygen Species |
url |
http://celljournal.org/journal/article/19692/download |
work_keys_str_mv |
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