Evidence map›Paper›PMID 25088424›Full record

ArticleCell reports2014

Birthdate and outgrowth timing predict cellular mechanisms of axon target matching in the developing visual pathway.

Jessica A Osterhout, Rana N El-Danaf, Phong L Nguyen, Andrew D Huberman

Abstract read
In one paragraph

Article in Cell reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing 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

54 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Mapping the Retina onto the Brain.Cold Spring Harbor perspectives in biology · 2024
    Review
  6. Article
  7. Semaphorin-6D and Plexin-A1 Act in a Non-Cell-Autonomous Manner to Position and Target Retinal Ganglion Cell Axons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  8. Temporal regulation of neural diversity in Drosophila and vertebrates.Seminars in cell & developmental biology · 2023
    Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. A cell-ECM mechanism for connecting the ipsilateral eye to the brain.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  16. Neural specification, targeting, and circuit formation during visual system assembly.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  17. Review
  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

4 authors.

Jessica A OsterhoutNeurobiology Section, Division of Biology, University of California, San Diego, La Jolla, CA 92093, USA.
Rana N El-DanafNeurobiology Section, Division of Biology, University of California, San Diego, La Jolla, CA 92093, USA; Neurosciences Department, University of California, San Diego, La Jolla, CA 92093, USA.
Phong L NguyenNeurobiology Section, Division of Biology, University of California, San Diego, La Jolla, CA 92093, USA; Neurosciences Department, University of California, San Diego, La Jolla, CA 92093, USA.
Andrew D HubermanNeurobiology Section, Division of Biology, University of California, San Diego, La Jolla, CA 92093, USA; Neurosciences Department, University of California, San Diego, La Jolla, CA 92093, USA; Department of Ophthalmology, University of California, San Diego, La Jolla, CA 92093, USA. Electronic address: ahuberman@ucsd.edu.

Funding

Development of retinofugal parallel pathwaysR01EY022157 · NEI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI HUBERMAN, ANDREW D · 2012 to 2016
$1.9M
NEI NIH HHS R01 EY022157NEI NIH HHS R01EY022157-01
6 · The paper itself

Abstract

How axons select their appropriate targets in the brain remains poorly understood. Here, we explore the cellular mechanisms of axon target matching in the developing visual system by comparing four transgenic mouse lines, each with a different population of genetically labeled retinal ganglion cells (RGCs) that connect to unique combinations of brain targets. We find that the time when an RGC axon arrives in the brain is correlated with its target selection strategy. Early-born, early-arriving RGC axons initially innervate multiple targets. Subsequently, most of those connections are removed. By contrast, later-born, later-arriving RGC axons are highly accurate in their initial target choices. These data reveal the diversity of cellular mechanisms that mammalian CNS axons use to pick their targets and highlight the key role of birthdate and outgrowth timing in influencing this precision. Timing-based mechanisms may underlie the assembly of the other sensory pathways and complex neural circuitry in the brain.

Indexed as

AnimalsApoptosisAxonsCadherinsFemaleMice, TransgenicOptic ChiasmReceptors, Dopamine D4RetinaRetinal Ganglion CellsVisual CortexCadherinsDrd4 protein, mouseReceptors, Dopamine D4

Identifiers

PMID25088424
PMCPMC4143387

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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.