Evidence map›Paper›PMID 27524481›Full record

ArticleCurrent biology : CB2016

Mismatch of Synaptic Patterns between Neurons Produced in Regeneration and during Development of the Vertebrate Retina.

Florence D D'Orazi, Xiao-Feng Zhao, Rachel O Wong, Takeshi Yoshimatsu

Abstract read
In one paragraph

Article in Current biology : CB, 2016. 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
–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

25 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Cell-Based Therapies: Strategies for Regeneration.Cold Spring Harbor perspectives in medicine · 2023
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Retinal regeneration requires dynamic Notch signaling.Neural regeneration research · 2022
    Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Noninvasive Imaging of Cone Ablation and Regeneration in Zebrafish.Translational vision science & technology · 2020
    Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Florence D D'OraziDepartment of Biological Structure, University of Washington, 1959 NE Pacific Street, Box 357420, Seattle, WA 98195, USA.
Xiao-Feng ZhaoDepartment of Cell and Developmental Biology, University of Michigan, Ann Arbor, MI 48109, USA.
Rachel O WongDepartment of Biological Structure, University of Washington, 1959 NE Pacific Street, Box 357420, Seattle, WA 98195, USA. Electronic address: wongr2@uw.edu.
Takeshi YoshimatsuDepartment of Biological Structure, University of Washington, 1959 NE Pacific Street, Box 357420, Seattle, WA 98195, USA. Electronic address: tyoshi@uw.edu.

Funding

Vision Research CoreP30EY001730 · NEI · UNIVERSITY OF WASHINGTON · PI MAUREEN E NEITZ · 1985 to 2026
$23.5M
VISUAL SCIENCES TRAINING PROGRAMT32EY007031 · NEI · UNIVERSITY OF WASHINGTON · PI Wyeth Daniel Bair, Anitha Pasupathy · 1985 to 2026
$6.1M
INTERDISCIPLINARY TRAINING IN DEVELOPMENTAL BIOLOGYT32HD007183 · NICHD · UNIVERSITY OF WASHINGTON · PI RAIBLE, DAVID W · 1985 to 2015
$5.7M
In Vivo Analysis of the Developing Vertebrate RetinaR01EY014358 · NEI · WASHINGTON UNIVERSITY · PI WONG, RACHEL O · 2003 to 2016
$4.3M
NEI NIH HHS P30 EY001730NEI NIH HHS R01 EY014358NEI NIH HHS T32 EY007031NICHD NIH HHS T32 HD007183
6 · The paper itself

Abstract

Stereotypic patterns of synaptic connections between neurons underlie the ability of the CNS to perform complex but circuit-specific information processing. Tremendous progress has been made toward advancing our understanding of how circuits are assembled during development, but whether the precision of this process can be recaptured after regeneration of neurons in the damaged CNS remains unclear. Here, we harnessed the endogenous regenerative capacity of the zebrafish retina to reconstruct the circuitry of neurons produced after damage. We tracked the input connectivity of identified bipolar cell (BC) types across stages of retinal development and after BC regeneration. We found that BCs of each type generate a unique and stereotypic wiring pattern with cone photoreceptors by gaining synapses with specific photoreceptor types over time. After selective ablation, the targeted BC types are rapidly reproduced and largely re-establish their characteristic morphological features. The regenerated population connects with appropriate photoreceptor types and establishes the original number of synaptic contacts. However, BC types that normally bias their connectivity in favor of red cones fail to precisely recapture this synaptic partner preference upon regeneration. Furthermore, regenerated BCs succeed in forming synaptic specializations at their axon terminals, but in excess of the usual number. Altogether, we find that regenerated BCs reinstate some, but not all, major features of their stereotypic wiring, suggesting that circuit patterns may be unable to regenerate with the same fidelity as in development.

Indexed as

RegenerationAnimalsAnimals, Genetically ModifiedNeuronsRetinaRetinal Cone Photoreceptor CellsSynapsesZebrafish

Identifiers

PMID27524481
PMCPMC5534240

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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.