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Metabolic profiling of zebrafish embryo development from blastula period to early larval stages
The zebrafish embryo is a popular model for drug screening, disease modelling and molecular genetics. In this study, samples were obtained from zebrafish at different developmental stages. The stages that were chosen were 3/4, 4/5, 24, 48, 72 and 96 hours post fertilization (hpf). Each sample includ...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6516655/ https://www.ncbi.nlm.nih.gov/pubmed/31086370 http://dx.doi.org/10.1371/journal.pone.0213661 |
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author | Dhillon, Sundeep S. Torell, Frida Donten, Magdalena Lundstedt-Enkel, Katrin Bennett, Kate Rännar, Stefan Trygg, Johan Lundstedt, Torbjörn |
author_facet | Dhillon, Sundeep S. Torell, Frida Donten, Magdalena Lundstedt-Enkel, Katrin Bennett, Kate Rännar, Stefan Trygg, Johan Lundstedt, Torbjörn |
author_sort | Dhillon, Sundeep S. |
collection | PubMed |
description | The zebrafish embryo is a popular model for drug screening, disease modelling and molecular genetics. In this study, samples were obtained from zebrafish at different developmental stages. The stages that were chosen were 3/4, 4/5, 24, 48, 72 and 96 hours post fertilization (hpf). Each sample included fifty embryos. The samples were analysed using gas chromatography time-of-flight mass spectrometry (GC-TOF-MS). Principle component analysis (PCA) was applied to get an overview of the data and orthogonal projection to latent structure discriminant analysis (OPLS-DA) was utilised to discriminate between the developmental stages. In this way, changes in metabolite profiles during vertebrate development could be identified. Using a GC-TOF-MS metabolomics approach it was found that nucleotides and metabolic fuel (glucose) were elevated at early stages of embryogenesis, whereas at later stages amino acids and intermediates in the Krebs cycle were abundant. This agrees with zebrafish developmental biology, as organs such as the liver and pancreas develop at later stages. Thus, metabolomics of zebrafish embryos offers a unique opportunity to investigate large scale changes in metabolic processes during important developmental stages in vertebrate development. In terms of stability of the metabolic profile and viability of the embryos, it was concluded at 72 hpf was a suitable time point for the use of zebrafish as a model system in numerous scientific applications. |
format | Online Article Text |
id | pubmed-6516655 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-65166552019-05-31 Metabolic profiling of zebrafish embryo development from blastula period to early larval stages Dhillon, Sundeep S. Torell, Frida Donten, Magdalena Lundstedt-Enkel, Katrin Bennett, Kate Rännar, Stefan Trygg, Johan Lundstedt, Torbjörn PLoS One Research Article The zebrafish embryo is a popular model for drug screening, disease modelling and molecular genetics. In this study, samples were obtained from zebrafish at different developmental stages. The stages that were chosen were 3/4, 4/5, 24, 48, 72 and 96 hours post fertilization (hpf). Each sample included fifty embryos. The samples were analysed using gas chromatography time-of-flight mass spectrometry (GC-TOF-MS). Principle component analysis (PCA) was applied to get an overview of the data and orthogonal projection to latent structure discriminant analysis (OPLS-DA) was utilised to discriminate between the developmental stages. In this way, changes in metabolite profiles during vertebrate development could be identified. Using a GC-TOF-MS metabolomics approach it was found that nucleotides and metabolic fuel (glucose) were elevated at early stages of embryogenesis, whereas at later stages amino acids and intermediates in the Krebs cycle were abundant. This agrees with zebrafish developmental biology, as organs such as the liver and pancreas develop at later stages. Thus, metabolomics of zebrafish embryos offers a unique opportunity to investigate large scale changes in metabolic processes during important developmental stages in vertebrate development. In terms of stability of the metabolic profile and viability of the embryos, it was concluded at 72 hpf was a suitable time point for the use of zebrafish as a model system in numerous scientific applications. Public Library of Science 2019-05-14 /pmc/articles/PMC6516655/ /pubmed/31086370 http://dx.doi.org/10.1371/journal.pone.0213661 Text en © 2019 Dhillon et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Dhillon, Sundeep S. Torell, Frida Donten, Magdalena Lundstedt-Enkel, Katrin Bennett, Kate Rännar, Stefan Trygg, Johan Lundstedt, Torbjörn Metabolic profiling of zebrafish embryo development from blastula period to early larval stages |
title | Metabolic profiling of zebrafish embryo development from blastula period to early larval stages |
title_full | Metabolic profiling of zebrafish embryo development from blastula period to early larval stages |
title_fullStr | Metabolic profiling of zebrafish embryo development from blastula period to early larval stages |
title_full_unstemmed | Metabolic profiling of zebrafish embryo development from blastula period to early larval stages |
title_short | Metabolic profiling of zebrafish embryo development from blastula period to early larval stages |
title_sort | metabolic profiling of zebrafish embryo development from blastula period to early larval stages |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6516655/ https://www.ncbi.nlm.nih.gov/pubmed/31086370 http://dx.doi.org/10.1371/journal.pone.0213661 |
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