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Small-extracellular vesicles and their microRNA cargo from porcine follicular fluids: the potential association with oocyte quality

BACKGROUND: Ovarian follicular fluids (FFs) contain several kinds of regulatory factors that maintain a suitable microenvironment for oocyte development. Extracellular vesicles (EVs) are among the factors that play essential roles in regulating follicle and oocyte development through their cargo mol...

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Autores principales: Gad, Ahmed, Murin, Matej, Bartkova, Alexandra, Kinterova, Veronika, Marcollova, Katerina, Laurincik, Jozef, Prochazka, Radek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9208166/
https://www.ncbi.nlm.nih.gov/pubmed/35725584
http://dx.doi.org/10.1186/s40104-022-00723-1
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author Gad, Ahmed
Murin, Matej
Bartkova, Alexandra
Kinterova, Veronika
Marcollova, Katerina
Laurincik, Jozef
Prochazka, Radek
author_facet Gad, Ahmed
Murin, Matej
Bartkova, Alexandra
Kinterova, Veronika
Marcollova, Katerina
Laurincik, Jozef
Prochazka, Radek
author_sort Gad, Ahmed
collection PubMed
description BACKGROUND: Ovarian follicular fluids (FFs) contain several kinds of regulatory factors that maintain a suitable microenvironment for oocyte development. Extracellular vesicles (EVs) are among the factors that play essential roles in regulating follicle and oocyte development through their cargo molecules that include microRNAs (miRNAs). This study aimed to investigate small-EV (s-EV) miRNAs in porcine FFs and their potential association with oocyte quality. METHODS: Individual aspirated oocytes were stained with lissamine green B stain (LB), a vital stain for oocyte quality, and each oocyte was classified as high-quality (unstained; HQ) or low-quality (stained; LQ). FFs corresponding to oocytes were pooled together into HQ and LQ groups. Small-EVs were isolated from FFs, characterized, and their miRNA cargo was identified using the Illumina NovaSeq sequencing platform. Additionally, s-EVs from the HQ and LQ groups were utilized to investigate their effect on oocyte development after co-incubation during in vitro maturation. RESULTS: A total of 19 miRNAs (including miR-125b, miR-193a-5p, and miR-320) were significantly upregulated, while 23 (including miR-9, miR-206, and miR-6516) were downregulated in the HQ compared to the LQ group. Apoptosis, p53 signaling, and cAMP signaling were among the top pathways targeted by the elevated miRNAs in the HQ group while oocyte meiosis, gap junction, and TGF-beta signaling were among the top pathways targeted by the elevated miRNAs in the LQ group. The supplementation of small-EVs during maturation does not affect the oocyte developmental rates. However, LQ s-EVs increase the proportion of oocytes with homogeneous mitochondrial distribution and decrease the proportion of heterogeneous distribution. CONCLUSION: Our findings indicated that FF-EVs contain different miRNA cargos associated with oocyte quality and could affect the mitochondrial distribution patterns during oocyte maturation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40104-022-00723-1.
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spelling pubmed-92081662022-06-21 Small-extracellular vesicles and their microRNA cargo from porcine follicular fluids: the potential association with oocyte quality Gad, Ahmed Murin, Matej Bartkova, Alexandra Kinterova, Veronika Marcollova, Katerina Laurincik, Jozef Prochazka, Radek J Anim Sci Biotechnol Research BACKGROUND: Ovarian follicular fluids (FFs) contain several kinds of regulatory factors that maintain a suitable microenvironment for oocyte development. Extracellular vesicles (EVs) are among the factors that play essential roles in regulating follicle and oocyte development through their cargo molecules that include microRNAs (miRNAs). This study aimed to investigate small-EV (s-EV) miRNAs in porcine FFs and their potential association with oocyte quality. METHODS: Individual aspirated oocytes were stained with lissamine green B stain (LB), a vital stain for oocyte quality, and each oocyte was classified as high-quality (unstained; HQ) or low-quality (stained; LQ). FFs corresponding to oocytes were pooled together into HQ and LQ groups. Small-EVs were isolated from FFs, characterized, and their miRNA cargo was identified using the Illumina NovaSeq sequencing platform. Additionally, s-EVs from the HQ and LQ groups were utilized to investigate their effect on oocyte development after co-incubation during in vitro maturation. RESULTS: A total of 19 miRNAs (including miR-125b, miR-193a-5p, and miR-320) were significantly upregulated, while 23 (including miR-9, miR-206, and miR-6516) were downregulated in the HQ compared to the LQ group. Apoptosis, p53 signaling, and cAMP signaling were among the top pathways targeted by the elevated miRNAs in the HQ group while oocyte meiosis, gap junction, and TGF-beta signaling were among the top pathways targeted by the elevated miRNAs in the LQ group. The supplementation of small-EVs during maturation does not affect the oocyte developmental rates. However, LQ s-EVs increase the proportion of oocytes with homogeneous mitochondrial distribution and decrease the proportion of heterogeneous distribution. CONCLUSION: Our findings indicated that FF-EVs contain different miRNA cargos associated with oocyte quality and could affect the mitochondrial distribution patterns during oocyte maturation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40104-022-00723-1. BioMed Central 2022-06-20 /pmc/articles/PMC9208166/ /pubmed/35725584 http://dx.doi.org/10.1186/s40104-022-00723-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Gad, Ahmed
Murin, Matej
Bartkova, Alexandra
Kinterova, Veronika
Marcollova, Katerina
Laurincik, Jozef
Prochazka, Radek
Small-extracellular vesicles and their microRNA cargo from porcine follicular fluids: the potential association with oocyte quality
title Small-extracellular vesicles and their microRNA cargo from porcine follicular fluids: the potential association with oocyte quality
title_full Small-extracellular vesicles and their microRNA cargo from porcine follicular fluids: the potential association with oocyte quality
title_fullStr Small-extracellular vesicles and their microRNA cargo from porcine follicular fluids: the potential association with oocyte quality
title_full_unstemmed Small-extracellular vesicles and their microRNA cargo from porcine follicular fluids: the potential association with oocyte quality
title_short Small-extracellular vesicles and their microRNA cargo from porcine follicular fluids: the potential association with oocyte quality
title_sort small-extracellular vesicles and their microrna cargo from porcine follicular fluids: the potential association with oocyte quality
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9208166/
https://www.ncbi.nlm.nih.gov/pubmed/35725584
http://dx.doi.org/10.1186/s40104-022-00723-1
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