Evidence map›Paper›PMID 22291895›Full record

ArticlePloS one2012

Microfluidic chips for in vivo imaging of cellular responses to neural injury in Drosophila larvae.

Mostafa Ghannad-Rezaie, Xing Wang, Bibhudatta Mishra, Catherine Collins, Nikos Chronis

Abstract readEvaluation Study
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing 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

46 citing papers in PubMed.

  1. Article
  2. Peripheral Nerve Crush inCold Spring Harbor protocols · 2025
    Article
  3. Study of Axonal Injury and Degeneration inCold Spring Harbor protocols · 2025
    Article
  4. Immobilizing Second-InstarCold Spring Harbor protocols · 2025
    Article
  5. Review
  6. Article
  7. Stac protein regulates release of neuropeptides.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  8. Modeling Neurodegenerative Disorders inInternational journal of molecular sciences · 2020
    Review
  9. Article
  10. Article
  11. Article
  12. An Immobilization Technique for Long-Term Time-Lapse Imaging of ExplantedFrontiers in cell and developmental biology · 2020
    Article
  13. Frontiers in Microfluidics, a Teaching Resource Review.Bioengineering (Basel, Switzerland) · 2019
    Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  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

5 authors.

Mostafa Ghannad-RezaieDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, Michigan, United States of America.
Xing Wang
Bibhudatta Mishra
Catherine Collins
Nikos Chronis

Funding

Regenerative and Degenerative Responses to Axonal InjuryR01NS069844 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CADIGAN, KENNETH M, COLLINS, CATHERINE A · 2010 to 2024
$5.0M
A MEMS intracranial pressure device for monitoring brain injuries and disordersR21NS062313 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CHRONIS, NIKOLAOS · 2009 to 2010
$381k
NINDS NIH HHS 5R21NS062313NINDS NIH HHS NS069844NINDS NIH HHS R01 NS069844NINDS NIH HHS R21 NS062313
6 · The paper itself

Abstract

With powerful genetics and a translucent cuticle, the Drosophila larva is an ideal model system for live imaging studies of neuronal cell biology and function. Here, we present an easy-to-use approach for high resolution live imaging in Drosophila using microfluidic chips. Two different designs allow for non-invasive and chemical-free immobilization of 3(rd) instar larvae over short (up to 1 hour) and long (up to 10 hours) time periods. We utilized these 'larva chips' to characterize several sub-cellular responses to axotomy which occur over a range of time scales in intact, unanaesthetized animals. These include waves of calcium which are induced within seconds of axotomy, and the intracellular transport of vesicles whose rate and flux within axons changes dramatically within 3 hours of axotomy. Axonal transport halts throughout the entire distal stump, but increases in the proximal stump. These responses precede the degeneration of the distal stump and regenerative sprouting of the proximal stump, which is initiated after a 7 hour period of dormancy and is associated with a dramatic increase in F-actin dynamics. In addition to allowing for the study of axonal regeneration in vivo, the larva chips can be utilized for a wide variety of in vivo imaging applications in Drosophila.

Indexed as

Gene Expression ProfilingOligonucleotide Array Sequence AnalysisAnimalsAxonal TransportAxonsAxotomyDiagnostic ImagingDrosophilaLarvaMicrofluidicsModels, BiologicalNerve RegenerationTime-Lapse ImagingTrauma, Nervous System

Identifiers

PMID22291895
PMCPMC3264548

What OpenQuestion holds

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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.