Evidence map›Paper›PMID 26290247›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2015

Netrin1-DCC-Mediated Attraction Guides Post-Crossing Commissural Axons in the Hindbrain.

Farnaz Shoja-Taheri, Arielle DeMarco, Grant S Mastick

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Neural regeneration research · 2018
    Article
  7. Article
  8. 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 at 2 institutions in 1 country.

Farnaz Shoja-TaheriDepartment of Biology, University of Nevada, Reno, Nevada 89557, and Department of Cell Biology and Human Anatomy, University of California, Davis School of Medicine, Davis, California 95616.
Arielle DeMarcoDepartment of Biology, University of Nevada, Reno, Nevada 89557, and.
Grant S MastickDepartment of Biology, University of Nevada, Reno, Nevada 89557, and gmastick@unr.edu.
University of Nevada, Reno · USUniversity of California, Davis · US

Funding

Outreach/Diversity/Pipeline ProjectP20GM103440 · NIGMS · UNIVERSITY OF NEVADA RENO · PI Eduardo A Robleto · 2012 to 2026
$58.0M
UNDERGRADUATE RESEARCH AND TRAININGP20RR016464 · NCRR · UNIVERSITY OF NEVADA RENO · PI REIBER, CARL · 2001 to 2011
$30.3M
Virtual Reality and Augmented Reality CoreP20GM103650 · NIGMS · UNIVERSITY OF NEVADA RENO · PI WEBSTER, MICHAEL A · 2012 to 2022
$20.9M
Cell Biology of Signaling across MembranesP20GM103554 · NIGMS · UNIVERSITY OF NEVADA RENO · PI VON BARTHELD, CHRISTOPHER S · 2012 to 2016
$8.0M
CELL BIOLOGY OF SIGNALING ACROSS MEMBRANESP20RR024210 · NCRR · UNIVERSITY OF NEVADA RENO · PI VON BARTHELD, CHRISTOPHER S · 2011 to 2011
$2.1M
Oculomotor axon guidance and neuron migrationR01EY025205 · NEI · UNIVERSITY OF NEVADA RENO · PI MASTICK, GRANT STEPHEN · 2015 to 2018
$1.4M
Longitudinal axon guidance by long range cues in the embryonic brainR01NS054740 · NINDS · UNIVERSITY OF NEVADA RENO · PI MASTICK, GRANT STEPHEN · 2008 to 2011
$1.0M
PIONEER AXON GUIDANCE IN THE EMBRYONIC FOREBRAINR01HD038069 · NICHD · UNIVERSITY OF NEVADA RENO · PI MASTICK, GRANT STEPHEN · 2001 to 2004
$800k
Motor neuron migration regulated by guidance cuesR21NS077169 · NINDS · UNIVERSITY OF NEVADA RENO · PI MASTICK, GRANT STEPHEN · 2012 to 2013
$368k
NCRR NIH HHS 1 P20 RR024210NCRR NIH HHS P20 RR016464NCRR NIH HHS P20 RR024210NEI NIH HHS R01 EY025205NICHD NIH HHS HD38069NICHD NIH HHS R01 HD038069NIGMS NIH HHS 1 P20 GM103650NIGMS NIH HHS P20 GM103440NIGMS NIH HHS P20 GM103440-11NIGMS NIH HHS P20 GM103554NIGMS NIH HHS P20 GM103650NINDS NIH HHS NS054740NINDS NIH HHS NS077169NINDS NIH HHS R01 NS054740NINDS NIH HHS R21 NS077169
6 · The paper itself

Abstract

Commissural axons grow along precise trajectories that are guided by several cues secreted from the ventral midline. After initial attraction to the floor plate using Netrin1 activation of its main attractive receptor, DCC (deleted in colorectal cancer), axons cross the ventral midline, and many turn to grow longitudinally on the contralateral side. After crossing the midline, axons are thought to lose their responsiveness to Netrin1 and become sensitive to midline Slit-Robo repulsion. We aimed to address the in vivo significance of Netrin1 in guiding post-crossing axon trajectories in mouse embryos. Surprisingly, in contrast to the spinal cord, Netrin1 and DCC mutants had abundant commissural axons crossing in the hindbrain. In Netrin1 and DCC mutants, many post-crossing axons made normal turns to grow longitudinally, but projected abnormally at angles away from the midline. In addition, exposure of cultured hindbrain explants to ectopic Netrin1 caused attractive deflection of post-crossing axons. Thus, Netrin1-DCC signaling is not required to attract pre-crossing axons toward the hindbrain floor plate, but is active in post-crossing guidance. Also in contrast with spinal cord, analysis of hindbrain post-crossing axons in Robo1/2 mutant embryos showed that Slit-Robo repulsive signaling was not required for post-crossing trajectories. Our findings show that Netrin1-DCC attractive signaling, but not Slit-Robo repulsive signaling, remains active in hindbrain post-crossing commissural axons to guide longitudinal trajectories, suggesting surprising regional diversity in commissural axon guidance mechanisms. SIGNIFICANCE STATEMENT: The left and right sides of the brainstem and spinal cord are connected primarily by axon fibers that grow across the ventral midline, and then away on the other side to their targets. Based on spinal cord, axons are initially attracted by diffusible attractive protein signals to approach and cross the midline, and then are thought to switch to repulsive cues to grow away on the opposite side. Our results in the hindbrain show that the major midline attractant, Netrin1, is not required for midline crossing. However, the post-crossing axons depend on Netrin1 attraction to set their proper trajectories on the other side. Overall, these findings suggest that commissural axons use distinct mechanisms to navigate in different CNS regions.

Indexed as

AnimalsAxonsCells, CulturedDCC ReceptorFemaleGene Expression Regulation, DevelopmentalMaleMiceNerve Growth FactorsNetrin-1NeurogenesisReceptors, Cell SurfaceRhombencephalonTumor Suppressor ProteinsDcc protein, mouseDCC ReceptorNerve Growth FactorsNetrin-1Receptors, Cell SurfaceTumor Suppressor Proteinsaxon guidancecommissural axonDCCNetrinRoboSlit

Identifiers

PMID26290247
PMCPMC4540804
OpenAlexW1608164220

What OpenQuestion holds

Textmetadata
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.