Evidence map›Paper›PMID 30081039›Full record

ArticleJournal of neuroscience methods2018

A microfluidic platform to study the effects of GDNF on neuronal axon entrapment.

Ze Zhong Wang, Matthew D Wood, Susan E Mackinnon, Shelly E Sakiyama-Elbert

Open access · greenAbstract read
In one paragraph

Article in Journal of neuroscience methods, 2018. 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
1.7field-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

5 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. GDNF Gene Therapy to Repair the Injured Peripheral Nerve.Frontiers in bioengineering and biotechnology · 2020
    Review
  5. 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 1 country.

Ze Zhong WangDepartment of Biomedical Engineering, Washington University in St. Louis, St. Louis, MO, United States.
Matthew D WoodDivision of Plastic and Reconstructive Surgery, Department of Surgery, Washington University School of Medicine, St. Louis, MO, United States.
Susan E MackinnonDivision of Plastic and Reconstructive Surgery, Department of Surgery, Washington University School of Medicine, St. Louis, MO, United States.
Shelly E Sakiyama-ElbertDepartment of Biomedical Engineering, University of Texas at Austin, Austin, TX, United States. Electronic address: sakiyama@utexas.edu.
Washington University in St. Louis · USThe University of Texas at Austin · US

Funding

THE EFFECTS OF GDNF ON PERIPHERAL NERVE REGENERATIONR01NS051706 · NINDS · WASHINGTON UNIVERSITY · PI MACKINNON, SUSAN E, SAKIYAMA-ELBERT, SHELLY ELESE · 2006 to 2016
$4.0M
NINDS NIH HHS R01 NS051706
6 · The paper itself

Abstract

backgroundOne potential treatment strategy to enhance axon regeneration is transplanting Schwann Cells (SCs) that overexpress glial cell line-derived neurotrophic factor (GDNF). Unfortunately, constitutive GDNF overexpression in vivo can result in failure of regenerating axons to extend beyond the GDNF source, a phenomenon termed the "candy-store" effect. Little is known about the mechanism of this axon entrapment in vivo. NEW

methodWe present a reproducible in vitro culture platform using a microfluidic device to model axon entrapment and investigate mechanisms by which GDNF causes axon entrapment. The device is comprised of three culture chambers connected by two sets of microchannels, which prevent cell soma from moving between chambers but allow neurites to grow between chambers. Neurons from dorsal root ganglia were seeded in one end chamber while the effect of different conditions in the other two chambers was used to study neurite entrapment.

resultsThe results showed that GDNF-overexpressing SCs (G-SCs) can induce axon entrapment in vitro. We also found that while physiological levels of GDNF (100 ng/mL) promoted neurite extension, supra-physiological levels of GDNF (700 ng/mL) induced axon entrapment. COMPARISON WITH EXISTING

methodAll previous work related to the "candy-store" effect were done in vivo. Here, we report the first in vitro platform that can recapitulate the axonal entrapment and investigate the mechanism of the phenomenon.

conclusionsThis platform facilitates investigation of the "candy-store" effect and shows the effects of high GDNF concentrations on neurite outgrowth.

Indexed as

Lab-On-A-Chip DevicesAnimalsAxon GuidanceAxonsCell Culture TechniquesChickensGanglia, SpinalGlial Cell Line-Derived Neurotrophic FactorMaleMicrofluidic Analytical TechniquesRats, Inbred LewSchwann CellsSensory Receptor CellsGlial Cell Line-Derived Neurotrophic FactorGene therapyNeurite extensionPeripheral nerve injurySchwann cells

Identifiers

PMID30081039
PMCPMC6200633
OpenAlexW2886715739

What OpenQuestion holds

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LicenceTDM
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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.