Evidence map›Paper›PMID 38449311›Full record

ArticleBiophysical journal2024

Dynamic temperature control in microfluidics for in vivo imaging of cold-sensing in C. elegans.

Sol Ah Lee, Yongmin Cho, William R Schafer, Hang Lu

Open access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.1field-weighted citation impact, top 26% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
  3. Automated Platforms inMicromachines · 2025
    Review
  4. Review
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

4 authors at 2 institutions in 2 countries.

Sol Ah LeeSchool of Chemical & Biomolecular Engineering, Georgia Institute of Technology, Atlanta Georgia.
Yongmin ChoSchool of Chemical & Biomolecular Engineering, Georgia Institute of Technology, Atlanta Georgia.
William R SchaferMedical Research Council Laboratory of Molecular Biology, Cambridge, United Kingdom.
Hang LuSchool of Chemical & Biomolecular Engineering, Georgia Institute of Technology, Atlanta Georgia. Electronic address: hang.lu@gatech.edu.
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 CouncilNIDCD NIH HHS R21 DC015652NINDS NIH HHS R01 NS096581
6 · The paper itself

Abstract

The ability to perceive temperature is crucial for most animals. It enables them to maintain their body temperature and swiftly react to noxiously cold or hot objects. Caenorhabditis elegans is a powerful genetic model for the study of thermosensation as its simple nervous system is well characterized and its transparent body is suited for in vivo functional imaging of neurons. The behavior triggered by experience-dependent thermosensation has been well studied in C. elegans under temperature-gradient environments. However, how C. elegans senses temperature via its nervous system is not well understood due to the limitations of currently available technologies. One major bottleneck is the difficulty in creating fast temperature changes, especially cold stimuli. Here, we developed a microfluidic-based platform that allowed the in vivo functional imaging of C. elegans responding to well-controlled temporally varying temperature stimulation by rapidly switching fluid streams at different temperatures. We used computational models to enable rational design and optimization of experimental conditions. We validated the design and utility of our system with studies of the functional role of thermosensory neurons. We showed that the responses of PVD polymodal nociceptor neurons observed in previous studies can be recapitulated. Further, we highlighted how this platform may be used to dissect neuronal circuits with an example of activity recording in PVC interneurons. Both of these neuron types show sensitization phenotypes. We envision that both the engineered system and the findings in this work will spur further studies of molecular and cellular mechanisms underlying cold-sensing through the nervous system.

Indexed as

Caenorhabditis elegansCaenorhabditis elegans ProteinsAnimalsCold TemperatureMicrofluidicsTemperatureThermosensingCaenorhabditis elegans Proteins

Identifiers

PMID38449311
PMCPMC11052694
OpenAlexW4392514245

What OpenQuestion holds

Textmetadata
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.