Evidence map›Paper›PMID 26116662›Full record

ArticleDevelopment (Cambridge, England)2015

Inhibitory neuron migration and IPL formation in the developing zebrafish retina.

Renee W Chow, Alexandra D Almeida, Owen Randlett, Caren Norden, William A Harris

Open access · hybridAbstract read
In one paragraph

Article in Development (Cambridge, England), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

25 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Article
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  4. Article
  5. Article
  6. Progenitor division and cell autonomous neurosecretion are required for rod photoreceptor sublaminar positioning.Proceedings of the National Academy of Sciences of the United States of America · 2023
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  11. Article
  12. Article
  13. Review
  14. Biology open · 2021
    Article
  15. Review
  16. Dendrite morphogenesis from birth to adulthood.Current opinion in neurobiology · 2018
    Review
  17. P2YMolecular neurobiology · 2018
    Article
  18. Article
  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

5 authors at 2 institutions in 3 countries.

Renee W ChowDepartment of Physiology, Development and Neuroscience, University of Cambridge, Cambridge CB2 3DY, UK.
Alexandra D AlmeidaDepartment of Physiology, Development and Neuroscience, University of Cambridge, Cambridge CB2 3DY, UK.
Owen RandlettDepartment of Physiology, Development and Neuroscience, University of Cambridge, Cambridge CB2 3DY, UK.
Caren NordenMPI of Molecular Cell Biology and Genetics, Pfotenhauerstraße 108, Dresden 01307, Germany norden@mpi-cbg.de wah20@cam.ac.uk.
William A HarrisDepartment of Physiology, Development and Neuroscience, University of Cambridge, Cambridge CB2 3DY, UK norden@mpi-cbg.de wah20@cam.ac.uk.
University of Cambridge · GBMax Planck Institute of Molecular Cell Biology and Genetics · DE

Funding

Wellcome Trust 100329Wellcome Trust 100329/Z/12/Z
6 · The paper itself

Abstract

The mature vertebrate retina is a highly ordered neuronal network of cell bodies and synaptic neuropils arranged in distinct layers. Little, however, is known about the emergence of this spatial arrangement. Here, we investigate how the three main types of retinal inhibitory neuron (RIN)--horizontal cells (HCs), inner nuclear layer amacrine cells (iACs) and displaced amacrine cells (dACs)--reach their specific laminar positions during development. Using in vivo time-lapse imaging of zebrafish retinas, we show that RINs undergo distinct phases of migration. The first phase, common to all RINs, is bipolar migration directed towards the apicobasal centre of the retina. All RINs then transition to a less directionally persistent multipolar phase of migration. Finally, HCs, iACs and dACs each undergo cell type-specific migration. In contrast to current hypotheses, we find that most dACs send processes into the forming inner plexiform layer (IPL) before migrating through it and inverting their polarity. By imaging and quantifying the dynamics of HCs, iACs and dACs from birth to final position, this study thus provides evidence for distinct and new migration patterns during retinal lamination and insights into the initiation of IPL formation.

Indexed as

AnimalsAnimals, Genetically ModifiedCell MovementImage Processing, Computer-AssistedKineticsMicroscopy, FluorescenceNeuronsRetinaTime-Lapse ImagingZebrafishAmacrine cellsDisplaced amacrine cellsHorizontal cellsInner plexiform layerNeuronal migration

Identifiers

PMID26116662
PMCPMC4529032
OpenAlexW2150578049

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.