Evidence map›Paper›PMID 28041904›Full record

ArticleDevelopmental cell2017

Long-Term High-Resolution Imaging of Developing C. elegans Larvae with Microfluidics.

Wolfgang Keil, Lena M Kutscher, Shai Shaham, Eric D Siggia

Abstract read
In one paragraph

Article in Developmental cell, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing 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

50 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. HarnessingSensors (Basel, Switzerland) · 2025
    Review
  5. Article
  6. Automated Platforms inMicromachines · 2025
    Review
  7. Article
  8. Article
  9. Visualization and Analyses of Cytoplasmic Streaming in C. elegans Zygotes.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article
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.

Wolfgang KeilCenter for Physics and Biology, The Rockefeller University, New York, NY 10065, USA; Laboratory of Developmental Genetics, The Rockefeller University, New York, NY 10065, USA. Electronic address: wkeil@rockefeller.edu.
Lena M KutscherLaboratory of Developmental Genetics, The Rockefeller University, New York, NY 10065, USA.
Shai ShahamLaboratory of Developmental Genetics, The Rockefeller University, New York, NY 10065, USA. Electronic address: shaham@rockefeller.edu.
Eric D SiggiaCenter for Physics and Biology, The Rockefeller University, New York, NY 10065, USA. Electronic address: siggiae@rockefeller.edu.

Funding

Genetics and Cell BiologyT32GM066699 · NIGMS · ROCKEFELLER UNIVERSITY · PI STRICKLAND, SIDNEY · 2004 to 2021
$7.6M
Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Aric L Daul, Ann E. Rougvie · 2012 to 2026
$7.5M
Glial control of sensory neuron functionR01NS064273 · NINDS · ROCKEFELLER UNIVERSITY · PI SHAHAM, SHAI · 2008 to 2017
$3.7M
Control of nonapoptotic C. elegans cell death similar to neurodegenerationR01NS081490 · NINDS · ROCKEFELLER UNIVERSITY · PI SHAHAM, SHAI · 2012 to 2017
$2.2M
Control of Linker Cell Death in C. elegansR01HD078703 · NICHD · ROCKEFELLER UNIVERSITY · PI SHAHAM, SHAI · 2014 to 2018
$1.7M
Glial control of sensory neuron receptive-ending shape and functionR01NS095795 · NINDS · ROCKEFELLER UNIVERSITY · PI SHAHAM, SHAI · 2017 to 2017
$371k
NICHD NIH HHS R01 HD078703NIGMS NIH HHS T32 GM066699NIH HHS P40 OD010440NINDS NIH HHS R01 NS064273NINDS NIH HHS R01 NS081490NINDS NIH HHS R01 NS095795
6 · The paper itself

Abstract

Long-term studies of Caenorhabditis elegans larval development traditionally require tedious manual observations because larvae must move to develop, and existing immobilization techniques either perturb development or are unsuited for young larvae. Here, we present a simple microfluidic device to simultaneously follow development of ten C. elegans larvae at high spatiotemporal resolution from hatching to adulthood (∼3 days). Animals grown in microchambers are periodically immobilized by compression to allow high-quality imaging of even weak fluorescence signals. Using the device, we obtain cell-cycle statistics for C. elegans vulval development, a paradigm for organogenesis. We combine Nomarski and multichannel fluorescence microscopy to study processes such as cell-fate specification, cell death, and transdifferentiation throughout post-embryonic development. Finally, we generate time-lapse movies of complex neural arborization through automated image registration. Our technique opens the door to quantitative analysis of time-dependent phenomena governing cellular behavior during C. elegans larval development.

Indexed as

Imaging, Three-DimensionalAnimalsCaenorhabditis elegansCell CycleCell DeathCell DivisionCell TrackingCell TransdifferentiationFemaleGene Expression Regulation, DevelopmentalLarvaMaleMicrofluidicsNeuritesTime FactorsTime-Lapse ImagingCaenorhabditis elegansdendritic arborizationlarval developmentlinker cell deathlong-term imagingmicrofluidicsPDA neuronPVD neurontransdifferentiationvulval development

Identifiers

PMID28041904
PMCPMC5263027

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.