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Extracellular vesicles shuttle protective messages against heat stress in bovine granulosa cells
Elevated summer temperature is reported to be the leading cause of stress in dairy and beef cows, which negatively affects various reproductive functions. Follicular cells respond to heat stress (HS) by activating the expression of heat shock family proteins (HSPs) and other antioxidants. HS is repo...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7519046/ https://www.ncbi.nlm.nih.gov/pubmed/32978452 http://dx.doi.org/10.1038/s41598-020-72706-z |
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author | Gebremedhn, Samuel Gad, Ahmed Aglan, Hoda Samir Laurincik, Jozef Prochazka, Radek Salilew-Wondim, Dessie Hoelker, Michael Schellander, Karl Tesfaye, Dawit |
author_facet | Gebremedhn, Samuel Gad, Ahmed Aglan, Hoda Samir Laurincik, Jozef Prochazka, Radek Salilew-Wondim, Dessie Hoelker, Michael Schellander, Karl Tesfaye, Dawit |
author_sort | Gebremedhn, Samuel |
collection | PubMed |
description | Elevated summer temperature is reported to be the leading cause of stress in dairy and beef cows, which negatively affects various reproductive functions. Follicular cells respond to heat stress (HS) by activating the expression of heat shock family proteins (HSPs) and other antioxidants. HS is reported to negatively affect the bi-directional communication between the follicular cells and the oocyte, which is partly mediated by follicular fluid extracellular vesicles (EVs) released from surrounding cells. As carriers of bioactive molecules (DNA, RNA, protein, and lipids), the involvement of EVs in mediating the stress response in follicular cells is not fully understood. Here we used an in vitro model to decipher the cellular and EV-coupled miRNAs of bovine granulosa cells in response to HS. Moreover, the protective role of stress-related EVs against subsequent HS was assessed. For this, bovine granulosa cells from smaller follicles were cultured in vitro and after sub-confluency, cells were either kept at 37 °C or subjected to HS (42 °C). Results showed that granulosa cells exposed to HS increased the accumulation of ROS, total oxidized protein, apoptosis, and the expression of HSPs and antioxidants, while the viability of cells was reduced. Moreover, 14 and 6 miRNAs were differentially expressed in heat-stressed granulosa cells and the corresponding EVs, respectively. Supplementation of stress-related EVs in cultured granulosa cells has induced adaptive response to subsequent HS. However, this potential was not pronounced when the cells were kept under 37 °C. Taking together, EVs generated from granulosa cells exposed to HS has the potential to shuttle bioactive molecules to recipient cells and make them robust to subsequent HS. |
format | Online Article Text |
id | pubmed-7519046 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75190462020-09-29 Extracellular vesicles shuttle protective messages against heat stress in bovine granulosa cells Gebremedhn, Samuel Gad, Ahmed Aglan, Hoda Samir Laurincik, Jozef Prochazka, Radek Salilew-Wondim, Dessie Hoelker, Michael Schellander, Karl Tesfaye, Dawit Sci Rep Article Elevated summer temperature is reported to be the leading cause of stress in dairy and beef cows, which negatively affects various reproductive functions. Follicular cells respond to heat stress (HS) by activating the expression of heat shock family proteins (HSPs) and other antioxidants. HS is reported to negatively affect the bi-directional communication between the follicular cells and the oocyte, which is partly mediated by follicular fluid extracellular vesicles (EVs) released from surrounding cells. As carriers of bioactive molecules (DNA, RNA, protein, and lipids), the involvement of EVs in mediating the stress response in follicular cells is not fully understood. Here we used an in vitro model to decipher the cellular and EV-coupled miRNAs of bovine granulosa cells in response to HS. Moreover, the protective role of stress-related EVs against subsequent HS was assessed. For this, bovine granulosa cells from smaller follicles were cultured in vitro and after sub-confluency, cells were either kept at 37 °C or subjected to HS (42 °C). Results showed that granulosa cells exposed to HS increased the accumulation of ROS, total oxidized protein, apoptosis, and the expression of HSPs and antioxidants, while the viability of cells was reduced. Moreover, 14 and 6 miRNAs were differentially expressed in heat-stressed granulosa cells and the corresponding EVs, respectively. Supplementation of stress-related EVs in cultured granulosa cells has induced adaptive response to subsequent HS. However, this potential was not pronounced when the cells were kept under 37 °C. Taking together, EVs generated from granulosa cells exposed to HS has the potential to shuttle bioactive molecules to recipient cells and make them robust to subsequent HS. Nature Publishing Group UK 2020-09-25 /pmc/articles/PMC7519046/ /pubmed/32978452 http://dx.doi.org/10.1038/s41598-020-72706-z Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Gebremedhn, Samuel Gad, Ahmed Aglan, Hoda Samir Laurincik, Jozef Prochazka, Radek Salilew-Wondim, Dessie Hoelker, Michael Schellander, Karl Tesfaye, Dawit Extracellular vesicles shuttle protective messages against heat stress in bovine granulosa cells |
title | Extracellular vesicles shuttle protective messages against heat stress in bovine granulosa cells |
title_full | Extracellular vesicles shuttle protective messages against heat stress in bovine granulosa cells |
title_fullStr | Extracellular vesicles shuttle protective messages against heat stress in bovine granulosa cells |
title_full_unstemmed | Extracellular vesicles shuttle protective messages against heat stress in bovine granulosa cells |
title_short | Extracellular vesicles shuttle protective messages against heat stress in bovine granulosa cells |
title_sort | extracellular vesicles shuttle protective messages against heat stress in bovine granulosa cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7519046/ https://www.ncbi.nlm.nih.gov/pubmed/32978452 http://dx.doi.org/10.1038/s41598-020-72706-z |
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