Evidence map›Paper›PMID 29340386›Full record

ArticleLab on a chip2018

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

Yongmin Cho, David N Oakland, Sol Ah Lee, William R Schafer, Hang Lu

Open access · hybridAbstract read
In one paragraph

Article in Lab on a chip, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.9field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 33 citations in OpenAlex.

  1. A gene expression atlas of a juvenile nervous system.bioRxiv : the preprint server for biology · 2025
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  11. ThemicroPublication biology · 2021
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 2 countries.

Yongmin ChoSchool of Chemical & Biomolecular Engineering, Georgia Institute of Technology, USA. hang.lu@gatech.edu.ORCID 0000-0002-8361-9612
David N OaklandSchool of Chemical & Biomolecular Engineering, Georgia Institute of Technology, USA. hang.lu@gatech.edu.
Sol Ah LeeSchool of Chemical & Biomolecular Engineering, Georgia Institute of Technology, USA. hang.lu@gatech.edu.
William R SchaferMedical Research Council Laboratory of Molecular Biology, Cambridge, UK.
Hang LuSchool of Chemical & Biomolecular Engineering, Georgia Institute of Technology, USA. hang.lu@gatech.edu.ORCID 0000-0002-6881-660X
Georgia Institute of Technology · USMRC Laboratory of Molecular Biology · GB

Funding

Quantitative Understanding of Mechnosensory Circuit on ChipR01NS096581 · NINDS · GEORGIA INSTITUTE OF TECHNOLOGY · PI LU, HANG · 2016 to 2020
$1.7M
An Assay to Screen for Drugs Against Transmembrane Proteins Associated with DeafnessR21DC015652 · NIDCD · GEORGIA INSTITUTE OF TECHNOLOGY · PI LU, HANG · 2017 to 2018
$386k
Medical Research Council MC_U105185857NIDCD NIH HHS R21 DC015652NINDS NIH HHS R01 NS096581Wellcome Trust
6 · The paper itself

Abstract

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.

Indexed as

Caenorhabditis elegansFunctional NeuroimagingLab-On-A-Chip DevicesMicrofluidic Analytical TechniquesStress, MechanicalAnimalsLarva

Identifiers

PMID29340386
PMCPMC5885276
OpenAlexW2782564370

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.