Evidence map›Paper›PMID 26616101›Full record

ArticleExperimental eye research2016

Tracking the fate of her4 expressing cells in the regenerating retina using her4:Kaede zebrafish.

Stephen G Wilson, Wen Wen, Lakshmi Pillai-Kastoori, Ann C Morris

Open access · greenAbstract read
In one paragraph

Article in Experimental eye research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

19 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Retinal regeneration requires dynamic Notch signaling.Neural regeneration research · 2022
    Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Notch signalling patterns retinal composition by regulatingDevelopment (Cambridge, England) · 2018
    Article
  13. Article
  14. Capn5 Expression in the Healthy and Regenerating Zebrafish Retina.Investigative ophthalmology & visual science · 2018
    Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. 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 at 1 institution in 1 country.

Stephen G WilsonDepartment of Biology, University of Kentucky, Lexington, 40506-0225, KY, USA.
Wen WenDepartment of Biology, University of Kentucky, Lexington, 40506-0225, KY, USA.
Lakshmi Pillai-KastooriDepartment of Biology, University of Kentucky, Lexington, 40506-0225, KY, USA.
Ann C MorrisDepartment of Biology, University of Kentucky, Lexington, 40506-0225, KY, USA. Electronic address: ann.morris@uky.edu.
University of Kentucky · US

Funding

ZEBRAFISH INTERNATIONAL RESOURCE CENTERP40RR012546 · NCRR · UNIVERSITY OF OREGON · PI WESTERFIELD, MONTE · 1998 to 2011
$21.9M
Vertebrate photoreceptor development and regenerationR01EY021769 · NEI · UNIVERSITY OF KENTUCKY · PI MORRIS, ANN C · 2012 to 2022
$3.2M
NCRR NIH HHS P40 RR012546NEI NIH HHS R01 EY021769
6 · The paper itself

Abstract

The Basic-Helix-Loop-Helix-Orange (bHLH-O) transcription factor Hairy-related 4 (her4) is a downstream effector of Notch-Delta signaling that represses expression of typically pro-neural genes in proliferative domains of the central nervous system. Notch-Delta signaling in the retina has been shown to increase in response to injury and influences neuroprotective properties of Müller glia. In contrast to mammals, teleost fish are able to regenerate retinal neurons in response to injury. In zebrafish, her4 is upregulated in the regenerating neural retina in response to both acute and chronic photoreceptor damage, but the contribution of her4 expressing cells to neurogenesis following acute or chronic retinal damage has remained unexplored. Here we investigate the role of her4 in the regenerating retina in a background of chronic, rod-specific degeneration as well as following acute light damage. We demonstrate that her4 is expressed in the persistently neurogenic ciliary marginal zone (CMZ), as well as in small subsets of slowly proliferating Müller glia in the inner nuclear layer (INL) of the central retina. We generated a transgenic line of zebrafish that expresses the photoconvertible Kaede reporter driven by a her4 promoter and validated that expression of the transgene faithfully recapitulates endogenous her4 expression. Lineage tracing analysis revealed that her4-expressing cells in the INL contribute to the rod lineage, and her4 expressing cells in the CMZ are capable of generating any retinal cell type except rod photoreceptors. Our results indicate that her4 is involved in a replenishing pathway that maintains populations of stem cells in the central retina, and that the magnitude of the her4-associated proliferative response mirrors the extent of retinal damage.

Indexed as

Gene Expression RegulationAnimalsAnimals, Genetically ModifiedApoptosisBasic Helix-Loop-Helix ProteinsCell DifferentiationCell ProliferationImmunohistochemistryIn Situ Hybridization, FluorescenceIn Situ Nick-End LabelingNerve RegenerationReal-Time Polymerase Chain ReactionRetinal DiseasesRetinal NeuronsRNAZebrafishBasic Helix-Loop-Helix Proteinsher4.1 protein, zebrafishRNAZebrafish ProteinsHer4Hes5Müller gliaRegenerationRetinaStem cellsZebrafish

Identifiers

PMID26616101
PMCPMC4842143
OpenAlexW2180489497

What OpenQuestion holds

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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.