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Integrated Microfluidic Device for Drug Studies of Early C. Elegans Embryogenesis
Small molecules inhibitors are powerful tools for studying multiple aspects of cell biology and stand at the forefront of drug discovery pipelines. However, in the early Caenorhabditis elegans (C. elegans) embryo, which is a powerful model system for cell and developmental biology, the use of small...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5980161/ https://www.ncbi.nlm.nih.gov/pubmed/29876206 http://dx.doi.org/10.1002/advs.201700751 |
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author | Dong, Li Jankele, Radek Cornaglia, Matteo Lehnert, Thomas Gönczy, Pierre Gijs, Martin A. M. |
author_facet | Dong, Li Jankele, Radek Cornaglia, Matteo Lehnert, Thomas Gönczy, Pierre Gijs, Martin A. M. |
author_sort | Dong, Li |
collection | PubMed |
description | Small molecules inhibitors are powerful tools for studying multiple aspects of cell biology and stand at the forefront of drug discovery pipelines. However, in the early Caenorhabditis elegans (C. elegans) embryo, which is a powerful model system for cell and developmental biology, the use of small molecule inhibitors has been limited by the impermeability of the embryonic eggshell, the low‐throughput manual embryo isolation methods, and the lack of well‐controlled drug delivery protocols. This work reports a fully integrated microfluidic approach for studies of C. elegans early embryogenesis, including the possibility of testing small molecule inhibitors with increased throughput and versatility. The setup enables robust on‐chip extraction of embryos from gravid adult worms in a dedicated pillar array chamber by mechanical compression, followed by rapid fluidic transfer of embryos into an adjacent microtrap array. Parallel analysis of ≈100 embryos by high‐resolution time‐lapse imaging from the one‐cell stage zygote until hatching can be performed with this device. The implementation of versatile microfluidic protocols, in particular time‐controlled and reversible drug delivery to on‐chip immobilized embryos, demonstrates the potential of the device for biochemical and pharmacological assays. |
format | Online Article Text |
id | pubmed-5980161 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-59801612018-06-06 Integrated Microfluidic Device for Drug Studies of Early C. Elegans Embryogenesis Dong, Li Jankele, Radek Cornaglia, Matteo Lehnert, Thomas Gönczy, Pierre Gijs, Martin A. M. Adv Sci (Weinh) Communications Small molecules inhibitors are powerful tools for studying multiple aspects of cell biology and stand at the forefront of drug discovery pipelines. However, in the early Caenorhabditis elegans (C. elegans) embryo, which is a powerful model system for cell and developmental biology, the use of small molecule inhibitors has been limited by the impermeability of the embryonic eggshell, the low‐throughput manual embryo isolation methods, and the lack of well‐controlled drug delivery protocols. This work reports a fully integrated microfluidic approach for studies of C. elegans early embryogenesis, including the possibility of testing small molecule inhibitors with increased throughput and versatility. The setup enables robust on‐chip extraction of embryos from gravid adult worms in a dedicated pillar array chamber by mechanical compression, followed by rapid fluidic transfer of embryos into an adjacent microtrap array. Parallel analysis of ≈100 embryos by high‐resolution time‐lapse imaging from the one‐cell stage zygote until hatching can be performed with this device. The implementation of versatile microfluidic protocols, in particular time‐controlled and reversible drug delivery to on‐chip immobilized embryos, demonstrates the potential of the device for biochemical and pharmacological assays. John Wiley and Sons Inc. 2018-03-08 /pmc/articles/PMC5980161/ /pubmed/29876206 http://dx.doi.org/10.1002/advs.201700751 Text en © 2018 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Communications Dong, Li Jankele, Radek Cornaglia, Matteo Lehnert, Thomas Gönczy, Pierre Gijs, Martin A. M. Integrated Microfluidic Device for Drug Studies of Early C. Elegans Embryogenesis |
title | Integrated Microfluidic Device for Drug Studies of Early C. Elegans Embryogenesis |
title_full | Integrated Microfluidic Device for Drug Studies of Early C. Elegans Embryogenesis |
title_fullStr | Integrated Microfluidic Device for Drug Studies of Early C. Elegans Embryogenesis |
title_full_unstemmed | Integrated Microfluidic Device for Drug Studies of Early C. Elegans Embryogenesis |
title_short | Integrated Microfluidic Device for Drug Studies of Early C. Elegans Embryogenesis |
title_sort | integrated microfluidic device for drug studies of early c. elegans embryogenesis |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5980161/ https://www.ncbi.nlm.nih.gov/pubmed/29876206 http://dx.doi.org/10.1002/advs.201700751 |
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