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Investigation of Metabolome Underlying the Biological Mechanisms of Acute Heat Stressed Granulosa Cells

Heat stress affects granulosa cells and the ovarian follicular microenvironment, ultimately resulting in poor oocyte developmental competence. This study aims to investigate the metabo-lomics response of bovine granulosa cells (bGCs) to in vitro acute heat stress of 43 °C. Heat stress triggers oxida...

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Autores principales: Sammad, Abdul, Hu, Lirong, Luo, Hanpeng, Abbas, Zaheer, Umer, Saqib, Zhao, Shanjiang, Xu, Qing, Khan, Adnan, Wang, Yajing, Zhu, Huabin, Wang, Yachun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8879866/
https://www.ncbi.nlm.nih.gov/pubmed/35216260
http://dx.doi.org/10.3390/ijms23042146
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author Sammad, Abdul
Hu, Lirong
Luo, Hanpeng
Abbas, Zaheer
Umer, Saqib
Zhao, Shanjiang
Xu, Qing
Khan, Adnan
Wang, Yajing
Zhu, Huabin
Wang, Yachun
author_facet Sammad, Abdul
Hu, Lirong
Luo, Hanpeng
Abbas, Zaheer
Umer, Saqib
Zhao, Shanjiang
Xu, Qing
Khan, Adnan
Wang, Yajing
Zhu, Huabin
Wang, Yachun
author_sort Sammad, Abdul
collection PubMed
description Heat stress affects granulosa cells and the ovarian follicular microenvironment, ultimately resulting in poor oocyte developmental competence. This study aims to investigate the metabo-lomics response of bovine granulosa cells (bGCs) to in vitro acute heat stress of 43 °C. Heat stress triggers oxidative stress-mediated apoptosis in cultured bGCs. Heat-stressed bGCs exhibited a time-dependent recovery of proliferation potential by 48 h. A total of 119 metabolites were identified through LC–MS/MS-based metabolomics of the spent culture media, out of which, 37 metabolites were determined as differentially involved in metabolic pathways related to bioenergetics support mechanisms and the physical adaptations of bGCs. Multiple analyses of metabolome data identified choline, citric acid, 3-hydroxy-3-methylglutaric acid, glutamine, and glycocyamine as being upregulated, while galactosamine, AICAR, ciliatine, 16-hydroxyhexadecanoic acid, lysine, succinic acid, uridine, xanthine, and uraconic acid were the important downregulated metabolites in acute heat stress. These differential metabolites were implicated in various important metabolic pathways directed towards bioenergetics support mechanisms including glycerophospholipid metabolism, the citrate cycle (TCA cycle), glyoxylate and dicarboxylate metabolism, and serine, threonine, and tyrosine metabolism. Our study presents important metabolites and metabolic pathways involved in the adaptation of bGCs to acute heat stress in vitro.
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spelling pubmed-88798662022-02-26 Investigation of Metabolome Underlying the Biological Mechanisms of Acute Heat Stressed Granulosa Cells Sammad, Abdul Hu, Lirong Luo, Hanpeng Abbas, Zaheer Umer, Saqib Zhao, Shanjiang Xu, Qing Khan, Adnan Wang, Yajing Zhu, Huabin Wang, Yachun Int J Mol Sci Article Heat stress affects granulosa cells and the ovarian follicular microenvironment, ultimately resulting in poor oocyte developmental competence. This study aims to investigate the metabo-lomics response of bovine granulosa cells (bGCs) to in vitro acute heat stress of 43 °C. Heat stress triggers oxidative stress-mediated apoptosis in cultured bGCs. Heat-stressed bGCs exhibited a time-dependent recovery of proliferation potential by 48 h. A total of 119 metabolites were identified through LC–MS/MS-based metabolomics of the spent culture media, out of which, 37 metabolites were determined as differentially involved in metabolic pathways related to bioenergetics support mechanisms and the physical adaptations of bGCs. Multiple analyses of metabolome data identified choline, citric acid, 3-hydroxy-3-methylglutaric acid, glutamine, and glycocyamine as being upregulated, while galactosamine, AICAR, ciliatine, 16-hydroxyhexadecanoic acid, lysine, succinic acid, uridine, xanthine, and uraconic acid were the important downregulated metabolites in acute heat stress. These differential metabolites were implicated in various important metabolic pathways directed towards bioenergetics support mechanisms including glycerophospholipid metabolism, the citrate cycle (TCA cycle), glyoxylate and dicarboxylate metabolism, and serine, threonine, and tyrosine metabolism. Our study presents important metabolites and metabolic pathways involved in the adaptation of bGCs to acute heat stress in vitro. MDPI 2022-02-15 /pmc/articles/PMC8879866/ /pubmed/35216260 http://dx.doi.org/10.3390/ijms23042146 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sammad, Abdul
Hu, Lirong
Luo, Hanpeng
Abbas, Zaheer
Umer, Saqib
Zhao, Shanjiang
Xu, Qing
Khan, Adnan
Wang, Yajing
Zhu, Huabin
Wang, Yachun
Investigation of Metabolome Underlying the Biological Mechanisms of Acute Heat Stressed Granulosa Cells
title Investigation of Metabolome Underlying the Biological Mechanisms of Acute Heat Stressed Granulosa Cells
title_full Investigation of Metabolome Underlying the Biological Mechanisms of Acute Heat Stressed Granulosa Cells
title_fullStr Investigation of Metabolome Underlying the Biological Mechanisms of Acute Heat Stressed Granulosa Cells
title_full_unstemmed Investigation of Metabolome Underlying the Biological Mechanisms of Acute Heat Stressed Granulosa Cells
title_short Investigation of Metabolome Underlying the Biological Mechanisms of Acute Heat Stressed Granulosa Cells
title_sort investigation of metabolome underlying the biological mechanisms of acute heat stressed granulosa cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8879866/
https://www.ncbi.nlm.nih.gov/pubmed/35216260
http://dx.doi.org/10.3390/ijms23042146
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