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Nano-Sampling and Reporter Tools to Study Metabolic Regulation in Zebrafish
In the past years, evidence has emerged that hallmarks of human metabolic disorders can be recapitulated in zebrafish using genetic, pharmacological or dietary interventions. An advantage of modeling metabolic diseases in zebrafish compared to other “lower organisms” is the presence of a vertebrate...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6401643/ https://www.ncbi.nlm.nih.gov/pubmed/30873407 http://dx.doi.org/10.3389/fcell.2019.00015 |
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author | Dickmeis, Thomas Feng, Yi Mione, Maria Caterina Ninov, Nikolay Santoro, Massimo Spaink, Herman P. Gut, Philipp |
author_facet | Dickmeis, Thomas Feng, Yi Mione, Maria Caterina Ninov, Nikolay Santoro, Massimo Spaink, Herman P. Gut, Philipp |
author_sort | Dickmeis, Thomas |
collection | PubMed |
description | In the past years, evidence has emerged that hallmarks of human metabolic disorders can be recapitulated in zebrafish using genetic, pharmacological or dietary interventions. An advantage of modeling metabolic diseases in zebrafish compared to other “lower organisms” is the presence of a vertebrate body plan providing the possibility to study the tissue-intrinsic processes preceding the loss of metabolic homeostasis. While the small size of zebrafish is advantageous in many aspects, it also has shortcomings such as the difficulty to obtain sufficient amounts for biochemical analyses in response to metabolic challenges. A workshop at the European Zebrafish Principal Investigator meeting in Trento, Italy, was dedicated to discuss the advantages and disadvantages of zebrafish to study metabolic disorders. This perspective article by the participants highlights strategies to achieve improved tissue-resolution for read-outs using “nano-sampling” approaches for metabolomics as well as live imaging of zebrafish expressing fluorescent reporter tools that inform on cellular or subcellular metabolic processes. We provide several examples, including the use of reporter tools to study the heterogeneity of pancreatic beta-cells within their tissue environment. While limitations exist, we believe that with the advent of new technologies and more labs developing methods that can be applied to minimal amounts of tissue or single cells, zebrafish will further increase their utility to study energy metabolism. |
format | Online Article Text |
id | pubmed-6401643 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-64016432019-03-14 Nano-Sampling and Reporter Tools to Study Metabolic Regulation in Zebrafish Dickmeis, Thomas Feng, Yi Mione, Maria Caterina Ninov, Nikolay Santoro, Massimo Spaink, Herman P. Gut, Philipp Front Cell Dev Biol Physiology In the past years, evidence has emerged that hallmarks of human metabolic disorders can be recapitulated in zebrafish using genetic, pharmacological or dietary interventions. An advantage of modeling metabolic diseases in zebrafish compared to other “lower organisms” is the presence of a vertebrate body plan providing the possibility to study the tissue-intrinsic processes preceding the loss of metabolic homeostasis. While the small size of zebrafish is advantageous in many aspects, it also has shortcomings such as the difficulty to obtain sufficient amounts for biochemical analyses in response to metabolic challenges. A workshop at the European Zebrafish Principal Investigator meeting in Trento, Italy, was dedicated to discuss the advantages and disadvantages of zebrafish to study metabolic disorders. This perspective article by the participants highlights strategies to achieve improved tissue-resolution for read-outs using “nano-sampling” approaches for metabolomics as well as live imaging of zebrafish expressing fluorescent reporter tools that inform on cellular or subcellular metabolic processes. We provide several examples, including the use of reporter tools to study the heterogeneity of pancreatic beta-cells within their tissue environment. While limitations exist, we believe that with the advent of new technologies and more labs developing methods that can be applied to minimal amounts of tissue or single cells, zebrafish will further increase their utility to study energy metabolism. Frontiers Media S.A. 2019-02-19 /pmc/articles/PMC6401643/ /pubmed/30873407 http://dx.doi.org/10.3389/fcell.2019.00015 Text en Copyright © 2019 Dickmeis, Feng, Mione, Ninov, Santoro, Spaink and Gut. http://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 | Physiology Dickmeis, Thomas Feng, Yi Mione, Maria Caterina Ninov, Nikolay Santoro, Massimo Spaink, Herman P. Gut, Philipp Nano-Sampling and Reporter Tools to Study Metabolic Regulation in Zebrafish |
title | Nano-Sampling and Reporter Tools to Study Metabolic Regulation in Zebrafish |
title_full | Nano-Sampling and Reporter Tools to Study Metabolic Regulation in Zebrafish |
title_fullStr | Nano-Sampling and Reporter Tools to Study Metabolic Regulation in Zebrafish |
title_full_unstemmed | Nano-Sampling and Reporter Tools to Study Metabolic Regulation in Zebrafish |
title_short | Nano-Sampling and Reporter Tools to Study Metabolic Regulation in Zebrafish |
title_sort | nano-sampling and reporter tools to study metabolic regulation in zebrafish |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6401643/ https://www.ncbi.nlm.nih.gov/pubmed/30873407 http://dx.doi.org/10.3389/fcell.2019.00015 |
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