Evidence map›Paper›PMID 26492970›Full record

ArticleNeural development2015

The LRR receptor Islr2 is required for retinal axon routing at the vertebrate optic chiasm.

Paolo Panza, Austen A Sitko, Hans-Martin Maischein, Iris Koch, Matthias Flötenmeyer, Gavin J Wright, Kenji Mandai, Carol A Mason, Christian Söllner

Open access · goldAbstract read
In one paragraph

Article in Neural development, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
0.7field-weighted citation impact, top 34% 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

21 citing papers in PubMed, 28 citations in OpenAlex.

  1. Time-resolved morphological and transcriptomic characterization of early enteric neuron subtype emergence in chick.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Article
  3. Article
  4. Development of the Binocular Circuit.Annual review of neuroscience · 2024
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Human iPSC-Derived Neuronal Cells FromFrontiers in neuroscience · 2020
    Article
  15. Article
  16. Wiring the Binocular Visual Pathways.International journal of molecular sciences · 2019
    Review
  17. Article
  18. Review
  19. Article
  20. 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

9 authors at 6 institutions in 4 countries.

Paolo PanzaMax-Planck-Institut für Entwicklungsbiologie, Abteilung Genetik, Spemannstraße 35, 72076, Tübingen, Germany. paolo.panza@tuebingen.mpg.de.
Austen A SitkoDepartment of Neuroscience, Columbia University, College of Physicians and Surgeons, 630 West 168th Street, New York, NY, 10032, USA.
Hans-Martin MaischeinMax-Planck-Institut für Entwicklungsbiologie, Abteilung Genetik, Spemannstraße 35, 72076, Tübingen, Germany.
Iris KochMax-Planck-Institut für Entwicklungsbiologie, Elektronenmikroskopie, Spemannstraße 35, 72076, Tübingen, Germany.
Matthias FlötenmeyerMax-Planck-Institut für Entwicklungsbiologie, Elektronenmikroskopie, Spemannstraße 35, 72076, Tübingen, Germany.
Gavin J WrightWellcome Trust Sanger Institute, Cell Surface Signalling Laboratory, Hinxton, Cambridge, CB10 1HH, UK.
Kenji MandaiDepartment of Biochemistry and Molecular Biology, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo-ku, Kobe, Hyogo, 650-0017, Japan.
Carol A MasonDepartment of Pathology & Cell Biology, Columbia University, College of Physicians and Surgeons, 630 West 168th Street, New York, NY, 10032, USA.
Christian SöllnerMax-Planck-Institut für Entwicklungsbiologie, Abteilung Genetik, Spemannstraße 35, 72076, Tübingen, Germany.
Columbia University · USMax Planck Institute for Developmental Biology · DEMax Planck Society · DEKobe University · JPMax Planck Institute for Heart and Lung Research · DEWellcome Sanger Institute · GB

Funding

GROWTH AND GUIDANCE OF RETINAL AXONSR01EY012736 · NEI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI MASON, CAROL A. · 1999 to 2017
$6.4M
NEI NIH HHS R01 EY 012736NEI NIH HHS R01 EY012736Wellcome Trust 098051
6 · The paper itself

Abstract

backgroundIn the visual system of most binocular vertebrates, the axons of retinal ganglion cells (RGCs) diverge at the diencephalic midline and extend to targets on both ipsi- and contralateral sides of the brain. While a molecular mechanism explaining ipsilateral guidance decisions has been characterized, less is known of how RGC axons cross the midline.

resultsHere, we took advantage of the zebrafish, in which all RGC axons project contralaterally at the optic chiasm, to characterize Islr2 as an RGC receptor required for complete retinal axon midline crossing. We used a systematic extracellular protein-protein interaction screening assay to identify two Vasorin paralogs, Vasna and Vasnb, as specific Islr2 ligands. Antibodies against Vasna and Vasnb reveal cellular populations surrounding the retinal axon pathway, suggesting the involvement of these proteins in guidance decisions made by axons of the optic nerve. Specifically, Vasnb marks the membranes of a cellular barricade located anteriorly to the optic chiasm, a structure termed the "glial knot" in higher vertebrates. Loss of function mutations in either vasorin paralog, individually or combined, however, do not exhibit an overt retinal axon projection phenotype, suggesting that additional midline factors, acting either independently or redundantly, compensate for their loss. Analysis of Islr2 knockout mice supports a scenario in which Islr2 controls the coherence of RGC axons through the ventral midline and optic tract.

conclusionsAlthough stereotypic guidance of RGC axons at the vertebrate optic chiasm is controlled by multiple, redundant mechanisms, and despite the differences in ventral diencephalic tissue architecture, we identify a novel role for the LRR receptor Islr2 in ensuring proper axon navigation at the optic chiasm of both zebrafish and mouse.

Indexed as

AnimalsAxonsBody PatterningImage Processing, Computer-AssistedIn Situ HybridizationMiceMice, Inbred C57BLNerve Tissue ProteinsNeurogenesisOptic ChiasmRetinaVisual PathwaysZebrafishLinx protein, mouseNerve Tissue Proteins

Identifiers

PMID26492970
PMCPMC4618557
OpenAlexW2151991426

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.