Cargando…
Multimodal Stimulation in a Microfluidic Device Facilitates Studies of Interneurons in Sensory Integration in C. elegans
Animals' perception and behavior involve integration of multiple sensory modalities. Caenorhabditis elegans is a useful model for studying multimodal sensory integration, as it has well‐characterized neuronal circuits in a relatively simple nervous system. However, most studies based on functio...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7720847/ https://www.ncbi.nlm.nih.gov/pubmed/32003130 http://dx.doi.org/10.1002/smll.201905852 |
_version_ | 1783619923945193472 |
---|---|
author | Cho, Yongmin Lee, Sol Ah Chew, Yee Lian Broderick, Kirby Schafer, William R. Lu, Hang |
author_facet | Cho, Yongmin Lee, Sol Ah Chew, Yee Lian Broderick, Kirby Schafer, William R. Lu, Hang |
author_sort | Cho, Yongmin |
collection | PubMed |
description | Animals' perception and behavior involve integration of multiple sensory modalities. Caenorhabditis elegans is a useful model for studying multimodal sensory integration, as it has well‐characterized neuronal circuits in a relatively simple nervous system. However, most studies based on functional imaging have only been conducted on single modal stimuli, because well‐controlled multimodal experiments for C. elegans are technically difficult. For instance, no single systems currently deliver precise stimuli with spatial, temporal, and intensity control, despite prior hypotheses that interneurons do integrate these sensory inputs to control behavior. Here, a microfluidic platform that can easily deliver spatially and temporally controlled combination stimuli to C. elegans is presented. With this platform, both sensory and interneuron activity is measured in response to mechanical and chemical stimulations in a quantitative and high‐throughput manner. It is found that the activity of command interneuron PVC can be modulated by prior stimulation both within the same and across different modalities. The roles of monoaminergic and peptidergic signaling are further examined on the process of multimodal integration through PVC activity. The approach exemplified here is envisioned to be broadly applicable in different contexts to elucidate underlying mechanisms and identify genes affecting multisensory integration. |
format | Online Article Text |
id | pubmed-7720847 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77208472020-12-11 Multimodal Stimulation in a Microfluidic Device Facilitates Studies of Interneurons in Sensory Integration in C. elegans Cho, Yongmin Lee, Sol Ah Chew, Yee Lian Broderick, Kirby Schafer, William R. Lu, Hang Small Full Papers Animals' perception and behavior involve integration of multiple sensory modalities. Caenorhabditis elegans is a useful model for studying multimodal sensory integration, as it has well‐characterized neuronal circuits in a relatively simple nervous system. However, most studies based on functional imaging have only been conducted on single modal stimuli, because well‐controlled multimodal experiments for C. elegans are technically difficult. For instance, no single systems currently deliver precise stimuli with spatial, temporal, and intensity control, despite prior hypotheses that interneurons do integrate these sensory inputs to control behavior. Here, a microfluidic platform that can easily deliver spatially and temporally controlled combination stimuli to C. elegans is presented. With this platform, both sensory and interneuron activity is measured in response to mechanical and chemical stimulations in a quantitative and high‐throughput manner. It is found that the activity of command interneuron PVC can be modulated by prior stimulation both within the same and across different modalities. The roles of monoaminergic and peptidergic signaling are further examined on the process of multimodal integration through PVC activity. The approach exemplified here is envisioned to be broadly applicable in different contexts to elucidate underlying mechanisms and identify genes affecting multisensory integration. John Wiley and Sons Inc. 2020-01-31 2020-03-12 /pmc/articles/PMC7720847/ /pubmed/32003130 http://dx.doi.org/10.1002/smll.201905852 Text en © 2020 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 | Full Papers Cho, Yongmin Lee, Sol Ah Chew, Yee Lian Broderick, Kirby Schafer, William R. Lu, Hang Multimodal Stimulation in a Microfluidic Device Facilitates Studies of Interneurons in Sensory Integration in C. elegans |
title | Multimodal Stimulation in a Microfluidic Device Facilitates Studies of Interneurons in Sensory Integration in C. elegans
|
title_full | Multimodal Stimulation in a Microfluidic Device Facilitates Studies of Interneurons in Sensory Integration in C. elegans
|
title_fullStr | Multimodal Stimulation in a Microfluidic Device Facilitates Studies of Interneurons in Sensory Integration in C. elegans
|
title_full_unstemmed | Multimodal Stimulation in a Microfluidic Device Facilitates Studies of Interneurons in Sensory Integration in C. elegans
|
title_short | Multimodal Stimulation in a Microfluidic Device Facilitates Studies of Interneurons in Sensory Integration in C. elegans
|
title_sort | multimodal stimulation in a microfluidic device facilitates studies of interneurons in sensory integration in c. elegans |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7720847/ https://www.ncbi.nlm.nih.gov/pubmed/32003130 http://dx.doi.org/10.1002/smll.201905852 |
work_keys_str_mv | AT choyongmin multimodalstimulationinamicrofluidicdevicefacilitatesstudiesofinterneuronsinsensoryintegrationincelegans AT leesolah multimodalstimulationinamicrofluidicdevicefacilitatesstudiesofinterneuronsinsensoryintegrationincelegans AT chewyeelian multimodalstimulationinamicrofluidicdevicefacilitatesstudiesofinterneuronsinsensoryintegrationincelegans AT broderickkirby multimodalstimulationinamicrofluidicdevicefacilitatesstudiesofinterneuronsinsensoryintegrationincelegans AT schaferwilliamr multimodalstimulationinamicrofluidicdevicefacilitatesstudiesofinterneuronsinsensoryintegrationincelegans AT luhang multimodalstimulationinamicrofluidicdevicefacilitatesstudiesofinterneuronsinsensoryintegrationincelegans |