Evidence map›Paper›PMID 32342988›Full record

ArticleThe Journal of comparative neurology2020

Conditional and biased regeneration of cone photoreceptor types in the zebrafish retina.

Florence D D'Orazi, Sachihiro C Suzuki, Nicole Darling, Rachel O Wong, Takeshi Yoshimatsu

Open access · hybridAbstract read
In one paragraph

Article in The Journal of comparative neurology, 2020. 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
2.3field-weighted citation impact, top 11% 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, 41 citations in OpenAlex.

  1. Article
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  7. New pathways to neurogenesis: Insights from injury-induced retinal regeneration.BioEssays : news and reviews in molecular, cellular and developmental biology · 2024
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Cell-Based Therapies: Strategies for Regeneration.Cold Spring Harbor perspectives in medicine · 2023
    Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Retinal Cone Mosaic in sws1-Mutant Medaka (Oryzias latipes), A Teleost.Investigative ophthalmology & visual science · 2022
    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 5 institutions in 3 countries.

Florence D D'OraziDepartment Biological Structure, University of Washington, Seattle, Washington, USA.
Sachihiro C SuzukiDepartment Biological Structure, University of Washington, Seattle, Washington, USA.
Nicole DarlingDepartment Biological Structure, University of Washington, Seattle, Washington, USA.
Rachel O WongDepartment Biological Structure, University of Washington, Seattle, Washington, USA.ORCID 0000-0001-5089-6296
Takeshi YoshimatsuDepartment Biological Structure, University of Washington, Seattle, Washington, USA.ORCID 0000-0002-4939-2020
Allen Institute for Brain Science · USDurham University · GBOkinawa Institute of Science and Technology Graduate University · JPUniversity of Sussex · GBUniversity of Washington · US

Funding

Vision Research CoreP30EY001730 · NEI · UNIVERSITY OF WASHINGTON · PI JAMES Bryant HURLEY · 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
REGULATION OF THE OUTER BLOOD-RETINAL BARRIERF32EY007031 · NEI · YALE UNIVERSITY · PI WILT, STEVEN D · 1999 to 2000
$11k
NEI NIH HHS F32 EY007031NEI NIH HHS P30 EY001730NEI NIH HHS R01 EY014358NEI NIH HHS T32 EY007031NICHD NIH HHS T32 HD007183
6 · The paper itself

Abstract

A major challenge in regenerative medicine is replacing cells lost through injury or disease. While significant progress has been made, much remains unknown about the accuracy of native regenerative programs in cell replacement. Here, we capitalized on the regenerative capacity and stereotypic retinal organization of zebrafish to determine the specificity with which retinal Müller glial cells replace lost neuronal cell types. By utilizing a targeted genetic ablation technique, we restricted death to all or to distinct cone photoreceptor types (red, blue, or UV-sensitive cones), enabling us to compare the composition of cones that are regenerated. We found that Müller glia produce cones of all types upon nondiscriminate ablation of these photoreceptors, or upon selective ablation of red or UV cones. Pan-ablation of cones led to regeneration of the various cone types in relative abundances that resembled those of nonablated controls, that is, red > green > UV ~ blue cones. Moreover, selective loss of red or UV cones biased production toward the cone type that was ablated. In contrast, ablation of blue cones alone largely failed to induce cone production at all, although it did induce cell division in Müller glia. The failure to produce cones upon selective elimination of blue cones may be due to their low abundance compared to other cone types. Alternatively, it may be that blue cone death alone does not trigger a change in progenitor competency to support cone genesis. Our findings add to the growing notion that cell replacement during regeneration does not perfectly mimic programs of cell generation during development.

Indexed as

AnimalsAnimals, Genetically ModifiedCell ProliferationNerve RegenerationNeurogliaRetinaRetinal Cone Photoreceptor CellsZebrafishcone genesisneuronal repairnitro-reductase cell ablationphotoreceptor cell proliferationretinal regenerationzebrafish photoreceptors

Identifiers

PMID32342988
PMCPMC8496684
OpenAlexW3017955852

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.