Evidence map›Paper›PMID 23115176›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2012

Axon sorting within the spinal cord marginal zone via Robo-mediated inhibition of N-cadherin controls spinocerebellar tract formation.

Nozomi Sakai, Ryan Insolera, Roy V Sillitoe, Song-Hai Shi, Zaven Kaprielian

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.1field-weighted citation impact, top 26% 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

24 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Structure of Long-Range Direct and Indirect Spinocerebellar Pathways as Well as Local Spinal Circuits Mediating Proprioception.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. The Cadherin Superfamily in Neural Circuit Assembly.Cold Spring Harbor perspectives in biology · 2018
    Review
  11. WGA-Alexa Conjugates for Axonal Tracing.Current protocols in neuroscience · 2017
    Article
  12. Sonic -'Jack-of-All-Trades' in Neural Circuit Formation.Journal of developmental biology · 2017
    Review
  13. Review
  14. Article
  15. Making sense out of spinal cord somatosensory development.Development (Cambridge, England) · 2016
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Morpholinos: studying gene function in the chick.Methods (San Diego, Calif.) · 2014
    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 at 3 institutions in 1 country.

Nozomi SakaiDominick P. Purpura Department of Neuroscience, Albert Einstein College of Medicine, Bronx, New York, 10461, USA.
Ryan Insolera
Roy V Sillitoe
Song-Hai Shi
Zaven Kaprielian
Albert Einstein College of Medicine · USCornell University · USMemorial Sloan Kettering Cancer Center · US

Funding

Axon Guidance in the Spinal CordR01NS038505 · NINDS · YESHIVA UNIVERSITY · PI KAPRIELIAN, ZAVEN · 2000 to 2010
$3.0M
NINDS NIH HHS R01 NS038505NINDS NIH HHS R01NS038505
6 · The paper itself

Abstract

The axons of spinal projection neurons transmit sensory information to the brain by ascending within highly organized longitudinal tracts. However, the molecular mechanisms that control the sorting of these axons within the spinal cord and their directed growth to poorly defined targets are not understood. Here, we show that an interplay between Robo and the cell adhesion molecule, N-cadherin, sorts spinal commissural axons into appropriate longitudinal tracts within the spinal cord, and thereby facilitates their brain targeting. Specifically, we show that d1 and d2 spinal commissural axons join the lateral funiculus within the spinal cord and target the cerebellum in chick embryos, and that these axons contribute to the spinocerebellar projection in transgenic reporter mice. Disabling Robo signaling or overexpressing N-cadherin on these axons prevents the formation of the lateral funiculus and the spinocerebellar tract, and simultaneously perturbing Robo and N-cadherin function rescues both phenotypes in chick embryos. Consistent with these observations, disabling Robo function in conditional N-cadherin knock-out mice results in a wild-type-like lateral funiculus. Together, these findings suggest that spinal projection axons must be sorted into distinct longitudinal tracts within the spinal cord proper to project to their brain targets.

Indexed as

AnimalsAxonsCadherinsCell AdhesionCerebellumChick EmbryoElectroporationFunctional LateralityMiceMice, KnockoutMutationNerve Tissue ProteinsPhenotypePlasmidsReceptors, Dopamine D1Receptors, Dopamine D2CadherinsNerve Tissue ProteinsReceptors, Dopamine D1Receptors, Dopamine D2Receptors, ImmunologicRoundabout Proteins

Identifiers

PMID23115176
PMCPMC3511830
OpenAlexW2146423671

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.