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Identification and Characterization of Extracellular Vesicles and Its DNA Cargo Secreted During Murine Embryo Development
Extracellular vesicles (EVs) are known to transport DNA, but their implications in embryonic implantation are unknown. The aim of this study was to investigate EVs production and secretion by preimplantation embryos and assess their DNA cargo. Murine oocytes and embryos were obtained from six- to ei...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7074575/ https://www.ncbi.nlm.nih.gov/pubmed/32079252 http://dx.doi.org/10.3390/genes11020203 |
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author | Simon, Blanca Bolumar, David Amadoz, Alicia Jimenez-Almazán, Jorge Valbuena, Diana Vilella, Felipe Moreno, Inmaculada |
author_facet | Simon, Blanca Bolumar, David Amadoz, Alicia Jimenez-Almazán, Jorge Valbuena, Diana Vilella, Felipe Moreno, Inmaculada |
author_sort | Simon, Blanca |
collection | PubMed |
description | Extracellular vesicles (EVs) are known to transport DNA, but their implications in embryonic implantation are unknown. The aim of this study was to investigate EVs production and secretion by preimplantation embryos and assess their DNA cargo. Murine oocytes and embryos were obtained from six- to eight-week-old females, cultured until E4.5 and analyzed using transmission electron microscopy to examine EVs production. EVs were isolated from E4.5-day conditioned media and quantified by nanoparticle tracking analysis, characterized by immunogold, and their DNA cargo sequenced. Multivesicular bodies were observed in murine oocytes and preimplantation embryos together with the secretion of EVs to the blastocoel cavity and blastocyst spent medium. Embryo-derived EVs showed variable electron-densities and sizes (20–500 nm) and total concentrations of 1.74 × 10(7) ± 2.60 × 10(6) particles/mL. Embryo secreted EVs were positive for CD63 and ARF6. DNA cargo sequencing demonstrated no differences in DNA between apoptotic bodies or smaller EVs, although they showed significant gene enrichment compared to control medium. The analysis of sequences uniquely mapping the murine genome revealed that DNA contained in EVs showed higher representation of embryo genome than vesicle-free DNA. Murine blastocysts secrete EVs containing genome-wide sequences of DNA to the medium, reinforcing the relevance of studying these vesicles and their cargo in the preimplantation moment, where secreted DNA may help the assessment of the embryo previous to implantation. |
format | Online Article Text |
id | pubmed-7074575 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-70745752020-03-20 Identification and Characterization of Extracellular Vesicles and Its DNA Cargo Secreted During Murine Embryo Development Simon, Blanca Bolumar, David Amadoz, Alicia Jimenez-Almazán, Jorge Valbuena, Diana Vilella, Felipe Moreno, Inmaculada Genes (Basel) Article Extracellular vesicles (EVs) are known to transport DNA, but their implications in embryonic implantation are unknown. The aim of this study was to investigate EVs production and secretion by preimplantation embryos and assess their DNA cargo. Murine oocytes and embryos were obtained from six- to eight-week-old females, cultured until E4.5 and analyzed using transmission electron microscopy to examine EVs production. EVs were isolated from E4.5-day conditioned media and quantified by nanoparticle tracking analysis, characterized by immunogold, and their DNA cargo sequenced. Multivesicular bodies were observed in murine oocytes and preimplantation embryos together with the secretion of EVs to the blastocoel cavity and blastocyst spent medium. Embryo-derived EVs showed variable electron-densities and sizes (20–500 nm) and total concentrations of 1.74 × 10(7) ± 2.60 × 10(6) particles/mL. Embryo secreted EVs were positive for CD63 and ARF6. DNA cargo sequencing demonstrated no differences in DNA between apoptotic bodies or smaller EVs, although they showed significant gene enrichment compared to control medium. The analysis of sequences uniquely mapping the murine genome revealed that DNA contained in EVs showed higher representation of embryo genome than vesicle-free DNA. Murine blastocysts secrete EVs containing genome-wide sequences of DNA to the medium, reinforcing the relevance of studying these vesicles and their cargo in the preimplantation moment, where secreted DNA may help the assessment of the embryo previous to implantation. MDPI 2020-02-17 /pmc/articles/PMC7074575/ /pubmed/32079252 http://dx.doi.org/10.3390/genes11020203 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Simon, Blanca Bolumar, David Amadoz, Alicia Jimenez-Almazán, Jorge Valbuena, Diana Vilella, Felipe Moreno, Inmaculada Identification and Characterization of Extracellular Vesicles and Its DNA Cargo Secreted During Murine Embryo Development |
title | Identification and Characterization of Extracellular Vesicles and Its DNA Cargo Secreted During Murine Embryo Development |
title_full | Identification and Characterization of Extracellular Vesicles and Its DNA Cargo Secreted During Murine Embryo Development |
title_fullStr | Identification and Characterization of Extracellular Vesicles and Its DNA Cargo Secreted During Murine Embryo Development |
title_full_unstemmed | Identification and Characterization of Extracellular Vesicles and Its DNA Cargo Secreted During Murine Embryo Development |
title_short | Identification and Characterization of Extracellular Vesicles and Its DNA Cargo Secreted During Murine Embryo Development |
title_sort | identification and characterization of extracellular vesicles and its dna cargo secreted during murine embryo development |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7074575/ https://www.ncbi.nlm.nih.gov/pubmed/32079252 http://dx.doi.org/10.3390/genes11020203 |
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