Cargando…

On-chip functional neuroimaging with mechanical stimulation in Caenorhabditis elegans larvae for studying development and neural circuits

Mechanosensation is fundamentally important for the abilities of an organism to experience touch, hear sounds, and maintain balance. Caenorhabditis elegans is a powerful system for studying mechanosensation as this worm is well suited for in vivo functional imaging of neurons. Many years of research...

Descripción completa

Detalles Bibliográficos
Autores principales: Cho, Yongmin, Oakland, David N., Lee, Sol Ah, Schafer, William R., Lu, Hang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5885276/
https://www.ncbi.nlm.nih.gov/pubmed/29340386
http://dx.doi.org/10.1039/c7lc01201b
_version_ 1783311952720691200
author Cho, Yongmin
Oakland, David N.
Lee, Sol Ah
Schafer, William R.
Lu, Hang
author_facet Cho, Yongmin
Oakland, David N.
Lee, Sol Ah
Schafer, William R.
Lu, Hang
author_sort Cho, Yongmin
collection PubMed
description Mechanosensation is fundamentally important for the abilities of an organism to experience touch, hear sounds, and maintain balance. Caenorhabditis elegans is a powerful system for studying mechanosensation as this worm is well suited for in vivo functional imaging of neurons. Many years of research using labor-intensive methods have generated a wealth of knowledge about mechanosensation in C. elegans, and the recent microfluidic-based platforms continue to push the boundary for this field. However, developmental aspects of sensory biology, including mechanosensation, are still not fully understood. One current bottleneck is the difficulty in assaying larvae because they are much smaller than adult worms. Microfluidic devices with features small enough for larvae, especially actuators for the delivery of mechanical stimulation, are difficult to design and fabricate. Here, we present a series of automatic microfluidic platforms that allow for in vivo functional imaging of C. elegans responding to controlled mechanical stimulation at different developmental stages. Using a novel fabrication method, we designed highly deformable pneumatically actuated on-chip structures that can deliver mechanical stimulation to larval worms. The PDMS actuator allows for quantitatively controlled mechanical stimulation of both gentle and harsh touch neurons, by simply changing the actuation pressure, which makes this device easily translatable to other labs. We validated the design and utility of our systems with studies of the functional role of mechanosensory neurons in developing worms; we showed that gentle and harsh touch neurons function similarly in early larvae as they do in the adult stage, which would not have been possible previously. Finally, we investigated the effect of a sleep-like state on neuronal responses by imaging C. elegans in the lethargus state.
format Online
Article
Text
id pubmed-5885276
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Royal Society of Chemistry
record_format MEDLINE/PubMed
spelling pubmed-58852762018-04-19 On-chip functional neuroimaging with mechanical stimulation in Caenorhabditis elegans larvae for studying development and neural circuits Cho, Yongmin Oakland, David N. Lee, Sol Ah Schafer, William R. Lu, Hang Lab Chip Chemistry Mechanosensation is fundamentally important for the abilities of an organism to experience touch, hear sounds, and maintain balance. Caenorhabditis elegans is a powerful system for studying mechanosensation as this worm is well suited for in vivo functional imaging of neurons. Many years of research using labor-intensive methods have generated a wealth of knowledge about mechanosensation in C. elegans, and the recent microfluidic-based platforms continue to push the boundary for this field. However, developmental aspects of sensory biology, including mechanosensation, are still not fully understood. One current bottleneck is the difficulty in assaying larvae because they are much smaller than adult worms. Microfluidic devices with features small enough for larvae, especially actuators for the delivery of mechanical stimulation, are difficult to design and fabricate. Here, we present a series of automatic microfluidic platforms that allow for in vivo functional imaging of C. elegans responding to controlled mechanical stimulation at different developmental stages. Using a novel fabrication method, we designed highly deformable pneumatically actuated on-chip structures that can deliver mechanical stimulation to larval worms. The PDMS actuator allows for quantitatively controlled mechanical stimulation of both gentle and harsh touch neurons, by simply changing the actuation pressure, which makes this device easily translatable to other labs. We validated the design and utility of our systems with studies of the functional role of mechanosensory neurons in developing worms; we showed that gentle and harsh touch neurons function similarly in early larvae as they do in the adult stage, which would not have been possible previously. Finally, we investigated the effect of a sleep-like state on neuronal responses by imaging C. elegans in the lethargus state. Royal Society of Chemistry 2018-02-21 2018-01-09 /pmc/articles/PMC5885276/ /pubmed/29340386 http://dx.doi.org/10.1039/c7lc01201b Text en This journal is © The Royal Society of Chemistry 2018 http://creativecommons.org/licenses/by/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0)
spellingShingle Chemistry
Cho, Yongmin
Oakland, David N.
Lee, Sol Ah
Schafer, William R.
Lu, Hang
On-chip functional neuroimaging with mechanical stimulation in Caenorhabditis elegans larvae for studying development and neural circuits
title On-chip functional neuroimaging with mechanical stimulation in Caenorhabditis elegans larvae for studying development and neural circuits
title_full On-chip functional neuroimaging with mechanical stimulation in Caenorhabditis elegans larvae for studying development and neural circuits
title_fullStr On-chip functional neuroimaging with mechanical stimulation in Caenorhabditis elegans larvae for studying development and neural circuits
title_full_unstemmed On-chip functional neuroimaging with mechanical stimulation in Caenorhabditis elegans larvae for studying development and neural circuits
title_short On-chip functional neuroimaging with mechanical stimulation in Caenorhabditis elegans larvae for studying development and neural circuits
title_sort on-chip functional neuroimaging with mechanical stimulation in caenorhabditis elegans larvae for studying development and neural circuits
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5885276/
https://www.ncbi.nlm.nih.gov/pubmed/29340386
http://dx.doi.org/10.1039/c7lc01201b
work_keys_str_mv AT choyongmin onchipfunctionalneuroimagingwithmechanicalstimulationincaenorhabditiseleganslarvaeforstudyingdevelopmentandneuralcircuits
AT oaklanddavidn onchipfunctionalneuroimagingwithmechanicalstimulationincaenorhabditiseleganslarvaeforstudyingdevelopmentandneuralcircuits
AT leesolah onchipfunctionalneuroimagingwithmechanicalstimulationincaenorhabditiseleganslarvaeforstudyingdevelopmentandneuralcircuits
AT schaferwilliamr onchipfunctionalneuroimagingwithmechanicalstimulationincaenorhabditiseleganslarvaeforstudyingdevelopmentandneuralcircuits
AT luhang onchipfunctionalneuroimagingwithmechanicalstimulationincaenorhabditiseleganslarvaeforstudyingdevelopmentandneuralcircuits