Evidence map›Paper›PMID 28466940›Full record

ArticleLab on a chip2017

Microfluidic platform with spatiotemporally controlled micro-environment for studying long-term C. elegans developmental arrests.

Weipeng Zhuo, Hang Lu, Patrick T McGrath

Abstract read
In one paragraph

Article in Lab on a chip, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. HarnessingSensors (Basel, Switzerland) · 2025
    Review
  2. Article
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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

3 authors.

Weipeng ZhuoSchool of Chemical & Biomolecular Engineering, Georgia Institute of Technology, Atlanta, GA 30332-0100, USA. hang.lu@gatech.edu.
Hang Lu
Patrick T McGrath

Funding

Quantitative microscopy-based rapid phenotyping and screeningR01GM088333 · NIGMS · GEORGIA INSTITUTE OF TECHNOLOGY · PI LU, HANG · 2011 to 2018
$2.3M
Functional characterization of an insulin-like peptide network that regulates learningR01GM108962 · NIGMS · HARVARD UNIVERSITY · PI ZHANG, YUN · 2014 to 2017
$2.2M
Quantitative Understanding of Mechnosensory Circuit on ChipR01NS096581 · NINDS · GEORGIA INSTITUTE OF TECHNOLOGY · PI LU, HANG · 2016 to 2020
$1.7M
Mechanistic understanding of age-dependent genetic architectureR01GM114170 · NIGMS · GEORGIA INSTITUTE OF TECHNOLOGY · PI MCGRATH, PATRICK T · 2015 to 2019
$1.5M
Automated droplet-based platform for combinatorial screens on whole animalsR21EB021676 · NIBIB · GEORGIA INSTITUTE OF TECHNOLOGY · PI LU, HANG · 2015 to 2016
$429k
Evolving multigenic extensions to lifespanR21AG050304 · NIA · GEORGIA INSTITUTE OF TECHNOLOGY · PI LU, HANG, MCGRATH, PATRICK T · 2015 to 2016
$391k
NIA NIH HHS R21 AG050304NIBIB NIH HHS R21 EB021676NIGMS NIH HHS R01 GM088333NIGMS NIH HHS R01 GM108962NIGMS NIH HHS R01 GM114170NINDS NIH HHS R01 NS096581
6 · The paper itself

Abstract

Animals' long-term survival is dependent on their ability to sense, filter and respond to their environment at multiple timescales. For example, during development, animals integrate environmental information, which can then modulate adult behavior and developmental trajectory. The neural and molecular mechanisms that underlie these changes are poorly understood. C. elegans is a powerful model organism to study such mechanisms; however, conventional plate-based culturing techniques are limited in their ability to consistently control and modulate an animal's environmental conditions. To address this need, we developed a microfluidics-based experimental platform capable of long-term culture of populations of developing C. elegans covering the L1 larval stage to adulthood, while achieving spatial consistency and temporal control of their environment. To prevent bacterial accumulation and maintain optimal flow characteristics and nutrient consistency over the operational period of over one hundred and fifty hours, several features of the microfluidic system and the peripheral equipment were optimized. By manipulating food and pheromone exposure over several days, we were able to demonstrate environmental-dependent changes to growth rate and entry to dauer, an alternative developmental state. We envision this system to be useful in studying the mechanisms underlying long timescale changes to behavior and development in response to environmental changes.

Indexed as

AnimalsCaenorhabditis elegansEquipment DesignImage Processing, Computer-AssistedLarvaMicrofluidic Analytical TechniquesPheromonesPheromones

Identifiers

PMID28466940
PMCPMC5521175

What OpenQuestion holds

Textmetadata
LicenceTDM
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.