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Automated and controlled mechanical stimulation and functional imaging in vivo in C. elegans
C. elegans is a useful genetic model system for investigating mechanisms involved in sensory behavior which are potentially relevant to human diseases. While utilities of advanced techniques such as microfluidics have accelerated some areas of C. elegans sensory biology such as chemosensation, studi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5575793/ https://www.ncbi.nlm.nih.gov/pubmed/28660945 http://dx.doi.org/10.1039/c7lc00465f |
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author | Cho, Yongmin Porto, Daniel A. Hwang, Hyundoo Grundy, Laura J. Schafer, William R. Lu, Hang |
author_facet | Cho, Yongmin Porto, Daniel A. Hwang, Hyundoo Grundy, Laura J. Schafer, William R. Lu, Hang |
author_sort | Cho, Yongmin |
collection | PubMed |
description | C. elegans is a useful genetic model system for investigating mechanisms involved in sensory behavior which are potentially relevant to human diseases. While utilities of advanced techniques such as microfluidics have accelerated some areas of C. elegans sensory biology such as chemosensation, studies of mechanosensation conventionally require immobilization by glue and manual delivery of stimuli, leading to low experimental throughput and high variability. Here we present a microfluidic platform that precisely and robustly delivers a wide range of mechanical stimuli and can also be used in conjunction with functional imaging and optical interrogation techniques. The platform is fully automated, thereby greatly enhancing the throughput and robustness of experiments. We show that the behavior of the well-known gentle and harsh touch neurons and their receptive fields can be recapitulated. Using calcium dynamics as a read-out, we demonstrate its ability to perform a drug screen in vivo. We envision that this system will be able to greatly accelerate the discovery of genes and molecules involved in mechanosensation and multimodal sensory behavior, as well as the discovery of therapeutics for related diseases. |
format | Online Article Text |
id | pubmed-5575793 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-55757932017-09-28 Automated and controlled mechanical stimulation and functional imaging in vivo in C. elegans Cho, Yongmin Porto, Daniel A. Hwang, Hyundoo Grundy, Laura J. Schafer, William R. Lu, Hang Lab Chip Chemistry C. elegans is a useful genetic model system for investigating mechanisms involved in sensory behavior which are potentially relevant to human diseases. While utilities of advanced techniques such as microfluidics have accelerated some areas of C. elegans sensory biology such as chemosensation, studies of mechanosensation conventionally require immobilization by glue and manual delivery of stimuli, leading to low experimental throughput and high variability. Here we present a microfluidic platform that precisely and robustly delivers a wide range of mechanical stimuli and can also be used in conjunction with functional imaging and optical interrogation techniques. The platform is fully automated, thereby greatly enhancing the throughput and robustness of experiments. We show that the behavior of the well-known gentle and harsh touch neurons and their receptive fields can be recapitulated. Using calcium dynamics as a read-out, we demonstrate its ability to perform a drug screen in vivo. We envision that this system will be able to greatly accelerate the discovery of genes and molecules involved in mechanosensation and multimodal sensory behavior, as well as the discovery of therapeutics for related diseases. Royal Society of Chemistry 2017-08-07 2017-06-13 /pmc/articles/PMC5575793/ /pubmed/28660945 http://dx.doi.org/10.1039/c7lc00465f Text en This journal is © The Royal Society of Chemistry 2017 http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution 3.0 Unported License (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Chemistry Cho, Yongmin Porto, Daniel A. Hwang, Hyundoo Grundy, Laura J. Schafer, William R. Lu, Hang Automated and controlled mechanical stimulation and functional imaging in vivo in C. elegans |
title | Automated and controlled mechanical stimulation and functional imaging in vivo in C. elegans
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title_full | Automated and controlled mechanical stimulation and functional imaging in vivo in C. elegans
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title_fullStr | Automated and controlled mechanical stimulation and functional imaging in vivo in C. elegans
|
title_full_unstemmed | Automated and controlled mechanical stimulation and functional imaging in vivo in C. elegans
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title_short | Automated and controlled mechanical stimulation and functional imaging in vivo in C. elegans
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title_sort | automated and controlled mechanical stimulation and functional imaging in vivo in c. elegans |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5575793/ https://www.ncbi.nlm.nih.gov/pubmed/28660945 http://dx.doi.org/10.1039/c7lc00465f |
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