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Granulosa Cells Improved Mare Oocyte Cytoplasmic Maturation by Providing Collagens
Assisted reproductive technology has important clinical applications and commercial values in the horse industry. However, this approach is limited largely by the low efficiency of oocyte in vitro maturation (IVM), especially cytoplasmic maturation. To improve the efficiency of mare oocyte IVM, we e...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9280134/ https://www.ncbi.nlm.nih.gov/pubmed/35846364 http://dx.doi.org/10.3389/fcell.2022.914735 |
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author | Zhu, Xinyuan Zhao, Shanshan Xu, Shibo Zhang, Dongyu Zhu, Minghui Pan, Qingjie Huang, Jiaojiao |
author_facet | Zhu, Xinyuan Zhao, Shanshan Xu, Shibo Zhang, Dongyu Zhu, Minghui Pan, Qingjie Huang, Jiaojiao |
author_sort | Zhu, Xinyuan |
collection | PubMed |
description | Assisted reproductive technology has important clinical applications and commercial values in the horse industry. However, this approach is limited largely by the low efficiency of oocyte in vitro maturation (IVM), especially cytoplasmic maturation. To improve the efficiency of mare oocyte IVM, we evaluated the effects of co-culture with cumulus–oocyte complexes (COCs) and granulosa cells (GCs) from follicles with small (<15 mm) and large diameters (>35 mm). Our results showed that oocyte nucleus maturation was not significantly improved by co-culturing with GCs. Interestingly, the cytoplasmic maturation of oocytes, defined by the distribution of cortical granules and mitochondria, as well as reactive oxygen species (ROS) levels, improved dramatically by co-culture with GCs, especially those derived from small follicles. Moreover, GCs promoted cumulus cell expansion by upregulating the expression of BMP15 in oocytes. To determine the mechanism underlying the effects of GCs, the transcriptomes of GCs from large and small follicles were compared. Expression levels of COL1A2, COL6A1, and COL6A2 were significantly higher in GCs from small follicles than in those from large follicles. These three genes were enriched in the extracellular matrix proteins-receptor interaction pathway and were involved in the regulation of collagens. Taken together, our results suggest that co-culture with GCs is beneficial to oocyte cytoplasmic maturation, and the increased expression of COL1A2, COL6A1, and COL6A2 improve the mare oocyte IVM system via the regulation of collagen. |
format | Online Article Text |
id | pubmed-9280134 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92801342022-07-15 Granulosa Cells Improved Mare Oocyte Cytoplasmic Maturation by Providing Collagens Zhu, Xinyuan Zhao, Shanshan Xu, Shibo Zhang, Dongyu Zhu, Minghui Pan, Qingjie Huang, Jiaojiao Front Cell Dev Biol Cell and Developmental Biology Assisted reproductive technology has important clinical applications and commercial values in the horse industry. However, this approach is limited largely by the low efficiency of oocyte in vitro maturation (IVM), especially cytoplasmic maturation. To improve the efficiency of mare oocyte IVM, we evaluated the effects of co-culture with cumulus–oocyte complexes (COCs) and granulosa cells (GCs) from follicles with small (<15 mm) and large diameters (>35 mm). Our results showed that oocyte nucleus maturation was not significantly improved by co-culturing with GCs. Interestingly, the cytoplasmic maturation of oocytes, defined by the distribution of cortical granules and mitochondria, as well as reactive oxygen species (ROS) levels, improved dramatically by co-culture with GCs, especially those derived from small follicles. Moreover, GCs promoted cumulus cell expansion by upregulating the expression of BMP15 in oocytes. To determine the mechanism underlying the effects of GCs, the transcriptomes of GCs from large and small follicles were compared. Expression levels of COL1A2, COL6A1, and COL6A2 were significantly higher in GCs from small follicles than in those from large follicles. These three genes were enriched in the extracellular matrix proteins-receptor interaction pathway and were involved in the regulation of collagens. Taken together, our results suggest that co-culture with GCs is beneficial to oocyte cytoplasmic maturation, and the increased expression of COL1A2, COL6A1, and COL6A2 improve the mare oocyte IVM system via the regulation of collagen. Frontiers Media S.A. 2022-06-30 /pmc/articles/PMC9280134/ /pubmed/35846364 http://dx.doi.org/10.3389/fcell.2022.914735 Text en Copyright © 2022 Zhu, Zhao, Xu, Zhang, Zhu, Pan and Huang. 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, Xinyuan Zhao, Shanshan Xu, Shibo Zhang, Dongyu Zhu, Minghui Pan, Qingjie Huang, Jiaojiao Granulosa Cells Improved Mare Oocyte Cytoplasmic Maturation by Providing Collagens |
title | Granulosa Cells Improved Mare Oocyte Cytoplasmic Maturation by Providing Collagens |
title_full | Granulosa Cells Improved Mare Oocyte Cytoplasmic Maturation by Providing Collagens |
title_fullStr | Granulosa Cells Improved Mare Oocyte Cytoplasmic Maturation by Providing Collagens |
title_full_unstemmed | Granulosa Cells Improved Mare Oocyte Cytoplasmic Maturation by Providing Collagens |
title_short | Granulosa Cells Improved Mare Oocyte Cytoplasmic Maturation by Providing Collagens |
title_sort | granulosa cells improved mare oocyte cytoplasmic maturation by providing collagens |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9280134/ https://www.ncbi.nlm.nih.gov/pubmed/35846364 http://dx.doi.org/10.3389/fcell.2022.914735 |
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