Evidence map›Paper›PMID 27784329›Full record

ArticleNeural development2016

Netrin1/DCC signaling promotes neuronal migration in the dorsal spinal cord.

Harald J Junge, Andrea R Yung, Lisa V Goodrich, Zhe Chen

Open access · goldAbstract read
In one paragraph

Article in Neural development, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

15 citing papers in PubMed, 27 citations in OpenAlex.

  1. Ontogeny of the spinal cord dorsal horn.Science (New York, N.Y.) · 2026
    Article
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  8. Transcriptional Control of Axon Guidance at Midline Structures.Frontiers in cell and developmental biology · 2022
    Review
  9. Pioneer Axons Utilize aThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  10. Review
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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

4 authors at 2 institutions in 1 country.

Harald J JungeDepartment of MCDB, University of Colorado, Boulder, CO, 80309, USA. harald.junge@colorado.edu.
Andrea R YungDepartment of Neurobiology, Harvard Medical School, Boston, MA, 02115, USA.
Lisa V GoodrichDepartment of Neurobiology, Harvard Medical School, Boston, MA, 02115, USA.
Zhe ChenDepartment of MCDB, University of Colorado, Boulder, CO, 80309, USA. zhe.chen@colorado.edu.ORCID 0000-0003-0683-9491
Harvard University · USUniversity of Colorado Boulder · US

Funding

Mouse Neurodevelopmental Behavior CoreU54HD090255 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI POMEROY, SCOTT LOREN · 2016 to 2020
$5.2M
Norrin Signaling in the Retina: Regulation of the Blood-Retina BarrierR01EY024261 · NEI · UNIVERSITY OF MINNESOTA · PI Harald Junge · 2014 to 2026
$4.7M
Non-sensory cells as a potential source for signaling molecules in the cochleaR21DC014916 · NIDCD · HARVARD MEDICAL SCHOOL · PI GOODRICH, LISA · 2016 to 2017
$450k
Functional characterization of Netrin-1 in the spiral ganglionF31DC014603 · NIDCD · HARVARD MEDICAL SCHOOL · PI YUNG, ANDREA · 2015 to 2016
$71k
NEI NIH HHS R01 EY024261NICHD NIH HHS U54 HD090255NIDCD NIH HHS F31 DC014603NIDCD NIH HHS R21 DC014916
6 · The paper itself

Abstract

backgroundNewborn neurons often migrate before undergoing final differentiation, extending neurites, and forming synaptic connections. Therefore, neuronal migration is crucial for establishing neural circuitry during development. In the developing spinal cord, neuroprogenitors first undergo radial migration within the ventricular zone. Differentiated neurons continue to migrate tangentially before reaching the final positions. The molecular pathways that regulate these migration processes remain largely unknown. Our previous study suggests that the DCC receptor is important for the migration of the dorsal spinal cord progenitors and interneurons. In this study, we determined the involvement of the Netrin1 ligand and the ROBO3 coreceptor in the migration.

resultsBy pulse labeling neuroprogenitors with electroporation, we examined their radial migration in Netrin1 (Ntn1), Dcc, and Robo3 knockout mice. We found that all three mutants exhibit delayed migration. Furthermore, using immunohistochemistry of the BARHL2 interneuron marker, we found that the mediolateral and dorsoventral migration of differentiated dorsal interneurons is also delayed. Together, our results suggest that Netrin1/DCC signaling induce neuronal migration in the dorsal spinal cord.

conclusionsNetrin1, DCC, and ROBO3 have been extensively studied for their functions in regulating axon guidance in the spinal commissural interneurons. We reveal that during earlier development of dorsal interneurons including commissural neurons, these molecules play an important role in promoting cell migration.

Indexed as

Cell MovementAnimalsDCC ReceptorInterneuronsMembrane ProteinsMiceMice, KnockoutNerve Growth FactorsNerve Tissue ProteinsNetrin-1Neural Stem CellsReceptors, Cell SurfaceRoundabout ProteinsSignal TransductionSpinal CordTumor Suppressor ProteinsDcc protein, mouseDCC ReceptorMembrane ProteinsNerve Growth FactorsNerve Tissue ProteinsNetrin-1Ntn1 protein, mouseReceptors, Cell SurfaceRobo3 protein, mouseRoundabout ProteinsTumor Suppressor ProteinsDCCNetrin1Neuronal migrationROBO3Spinal cord neurons

Identifiers

PMID27784329
PMCPMC5081974
OpenAlexW2540463125

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.