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Melatonin Modulates Lipid Metabolism in Porcine Cumulus–Oocyte Complex via Its Receptors

Lipid is a crucial energy resource for mammalian oocyte. Melatonin could benefit the maturation of porcine oocyte in vitro, but the related mechanism is not elucidated yet. In the current study, methods to monitor lipid metabolism in single live oocytes were firstly established using probes (Lipi-Bl...

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Autores principales: Zhu, Tianqi, Guan, Shengyu, Lv, Dongying, Zhao, Mengmeng, Yan, Laiqing, Shi, Li, Ji, Pengyun, Zhang, Lu, Liu, Guoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8047119/
https://www.ncbi.nlm.nih.gov/pubmed/33869202
http://dx.doi.org/10.3389/fcell.2021.648209
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author Zhu, Tianqi
Guan, Shengyu
Lv, Dongying
Zhao, Mengmeng
Yan, Laiqing
Shi, Li
Ji, Pengyun
Zhang, Lu
Liu, Guoshi
author_facet Zhu, Tianqi
Guan, Shengyu
Lv, Dongying
Zhao, Mengmeng
Yan, Laiqing
Shi, Li
Ji, Pengyun
Zhang, Lu
Liu, Guoshi
author_sort Zhu, Tianqi
collection PubMed
description Lipid is a crucial energy resource for mammalian oocyte. Melatonin could benefit the maturation of porcine oocyte in vitro, but the related mechanism is not elucidated yet. In the current study, methods to monitor lipid metabolism in single live oocytes were firstly established using probes (Lipi-Blue and Lipi-Green). It was observed that both lipid biogenesis and lipolysis occurred in maturing oocyte, but the general level of lipids dropped. Then maturing oocytes stained with probes were treated with melatonin or lipid metabolic-related inhibitors (triacsin C, rotenone, or etomoxir). The results showed that the lipid metabolism and maturation of porcine oocytes were all disrupted and that melatonin rescued the oocytes treated with triacsin C or rotenone, but not those treated with etomoxir. Further investigation demonstrated that cumulus cells are able to transfer lipids to oocytes via gap junctions. It was also observed that melatonin receptors exist in cumulus cells and are required for oocytes to maintain lipid metabolism. Meanwhile, the global gene expressing in cumulus cells was also modulated by melatonin, especially the genes related to antioxidants (SOD1, GPX1, GPX3, GPX4, PRDX2, and PRDX5), lipid metabolism (FABP3, FABP5, ACACB, TECR, etc.), and mitochondrial respiration (GPD1, ETFB, CYC1, and the genes of ATP synthase). Altogether the current research demonstrates that melatonin modulates lipid metabolism in maturing oocytes through its receptors in cumulus cells and benefits the developmental competence of oocytes.
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spelling pubmed-80471192021-04-16 Melatonin Modulates Lipid Metabolism in Porcine Cumulus–Oocyte Complex via Its Receptors Zhu, Tianqi Guan, Shengyu Lv, Dongying Zhao, Mengmeng Yan, Laiqing Shi, Li Ji, Pengyun Zhang, Lu Liu, Guoshi Front Cell Dev Biol Cell and Developmental Biology Lipid is a crucial energy resource for mammalian oocyte. Melatonin could benefit the maturation of porcine oocyte in vitro, but the related mechanism is not elucidated yet. In the current study, methods to monitor lipid metabolism in single live oocytes were firstly established using probes (Lipi-Blue and Lipi-Green). It was observed that both lipid biogenesis and lipolysis occurred in maturing oocyte, but the general level of lipids dropped. Then maturing oocytes stained with probes were treated with melatonin or lipid metabolic-related inhibitors (triacsin C, rotenone, or etomoxir). The results showed that the lipid metabolism and maturation of porcine oocytes were all disrupted and that melatonin rescued the oocytes treated with triacsin C or rotenone, but not those treated with etomoxir. Further investigation demonstrated that cumulus cells are able to transfer lipids to oocytes via gap junctions. It was also observed that melatonin receptors exist in cumulus cells and are required for oocytes to maintain lipid metabolism. Meanwhile, the global gene expressing in cumulus cells was also modulated by melatonin, especially the genes related to antioxidants (SOD1, GPX1, GPX3, GPX4, PRDX2, and PRDX5), lipid metabolism (FABP3, FABP5, ACACB, TECR, etc.), and mitochondrial respiration (GPD1, ETFB, CYC1, and the genes of ATP synthase). Altogether the current research demonstrates that melatonin modulates lipid metabolism in maturing oocytes through its receptors in cumulus cells and benefits the developmental competence of oocytes. Frontiers Media S.A. 2021-04-01 /pmc/articles/PMC8047119/ /pubmed/33869202 http://dx.doi.org/10.3389/fcell.2021.648209 Text en Copyright © 2021 Zhu, Guan, Lv, Zhao, Yan, Shi, Ji, Zhang and Liu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Zhu, Tianqi
Guan, Shengyu
Lv, Dongying
Zhao, Mengmeng
Yan, Laiqing
Shi, Li
Ji, Pengyun
Zhang, Lu
Liu, Guoshi
Melatonin Modulates Lipid Metabolism in Porcine Cumulus–Oocyte Complex via Its Receptors
title Melatonin Modulates Lipid Metabolism in Porcine Cumulus–Oocyte Complex via Its Receptors
title_full Melatonin Modulates Lipid Metabolism in Porcine Cumulus–Oocyte Complex via Its Receptors
title_fullStr Melatonin Modulates Lipid Metabolism in Porcine Cumulus–Oocyte Complex via Its Receptors
title_full_unstemmed Melatonin Modulates Lipid Metabolism in Porcine Cumulus–Oocyte Complex via Its Receptors
title_short Melatonin Modulates Lipid Metabolism in Porcine Cumulus–Oocyte Complex via Its Receptors
title_sort melatonin modulates lipid metabolism in porcine cumulus–oocyte complex via its receptors
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8047119/
https://www.ncbi.nlm.nih.gov/pubmed/33869202
http://dx.doi.org/10.3389/fcell.2021.648209
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