Evidence map›Paper›PMID 36533135›Full record

ArticleFrontiers in molecular neuroscience2022

Dynamic functional and structural remodeling during retinal regeneration in zebrafish.

Lindsey M Barrett, Diana M Mitchell, Peter C Meighan, Michael D Varnum, Deborah L Stenkamp

Open access · goldAbstract read
In one paragraph

Article in Frontiers in molecular neuroscience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 37% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. The Healthy and Diseased Retina Seen through Neuron-Glia Interactions.International journal of molecular sciences · 2024
    Review
  6. The regeneration-responsive elementFrontiers in molecular neuroscience · 2023
    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 1 country.

Lindsey M BarrettDepartment of Biological Sciences, University of Idaho, Moscow, ID, United States.
Diana M MitchellDepartment of Biological Sciences, University of Idaho, Moscow, ID, United States.
Peter C MeighanDepartment of Integrative Physiology and Neuroscience, Washington State University, Pullman, WA, United States.
Michael D VarnumDepartment of Integrative Physiology and Neuroscience, Washington State University, Pullman, WA, United States.
Deborah L StenkampDepartment of Biological Sciences, University of Idaho, Moscow, ID, United States.
University of Idaho · USWashington State University · US

Funding

Women's health: interplay of maternal diet and key demographics on neurological health in the rural frontier and remote WestP20GM103408 · NIGMS · UNIVERSITY OF IDAHO · PI Carolyn Hovde Bohach · 2012 to 2026
$59.8M
Patterning Genes in Retinal DevelopmentR01EY012146 · NEI · UNIVERSITY OF IDAHO · PI Deborah L Stenkamp · 2004 to 2026
$6.7M
Macrophage Determinants of Retinal RegenerationR01EY030467 · NEI · UNIVERSITY OF IDAHO · PI MITCHELL, DIANA · 2020 to 2024
$1.8M
Acquisition of a Dynamic Imaging SystemS10OD018044 · OD · UNIVERSITY OF IDAHO · PI STENKAMP, DEBORAH L · 2014 to 2014
$455k
Ubiquitin-system manipulations to probe and mitigate ethanol damage in neuronsR21AA028106 · NIAAA · WASHINGTON STATE UNIVERSITY · PI VARNUM, MICHAEL D. · 2021 to 2022
$396k
Synapses in Regenerated RetinaR21EY026814 · NEI · UNIVERSITY OF IDAHO · PI STENKAMP, DEBORAH L · 2016 to 2017
$388k
NEI NIH HHS R01 EY012146NEI NIH HHS R01 EY030467NEI NIH HHS R21 EY026814NIAAA NIH HHS R21 AA028106NIGMS NIH HHS P20 GM103408NIH HHS S10 OD018044
6 · The paper itself

Abstract

Introduction: Zebrafish regenerate their retinas following damage, resulting in restoration of visual function. Here we evaluate recovery of retinal function through qualitative and quantitative analysis of the electroretinogram (ERG) over time following retinal damage, in correlation to histological features of regenerated retinal tissue. Methods: Retinas of adult zebrafish were lesioned by intravitreal injection of 10 μM (extensive lesion; destroys all neurons) or 2 μM (selective lesion; spares photoreceptors) ouabain. Unlesioned contralateral retinas served as controls. Function of retinal circuitry was analyzed at selected timepoints using ERG recordings from live zebrafish, and whole eyes were processed for histological analyses immediately thereafter. Results: Qualitative and quantitative assessment of waveforms during retinal regeneration revealed dynamic changes that were heterogeneous on an individual level within each sampling time, but still followed common waveform recovery patterns on a per-fish and population-level basis. Early in the regeneration period (13-30 days post injury; DPI), for both lesion types, b-waves were essentially not detected, and unmasked increased apparent amplitudes, implicit times, and half-widths of a-waves (vs. controls). In control recordings, d-waves were not obviously detected, but apparent d-waves (OFF-bipolar responses) from regenerating retinas of several fish became prominent by 30DPI and dominated the post-photoreceptor response (PPR). Beyond 45DPI, b-waves became detectable, and the ratio of apparent d- to b-wave contributions progressively shifted with most, but not all, fish displaying a b-wave dominated PPR. At the latest timepoints (extensive, 90DPI; selective, 80DPI), recordings with measurable b-waves approached a normal waveform (implicit times and half-widths), but amplitudes were not restored to control levels. Histological analyses of the retinas from which ERGs were recorded showed that as regeneration progressed, PKCa + ON-bipolar terminals and parvalbumin + amacrine cell processes became more stereotypically positioned within the deep sublaminae of the INL over recovery time after each lesion type, consistent with the shift in PPR seen in the ERG recordings. Discussion: Taken together, these data suggest that photoreceptor-OFF-bipolar component/connectivity may functionally recover and mature earlier during regeneration compared to the photoreceptor-ON-bipolar component, though the timeframe in which such recovery happens is heterogeneous on a per-fish basis. Collectively our studies suggest gradual restoration of ON-bipolar functional circuitry during retinal regeneration.

Indexed as

electroretinographyERGOFF-bipolarON-bipolarregenerationretinaretinal bipolar cellzebrafish

Identifiers

PMID36533135
PMCPMC9748287
OpenAlexW4310995249

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.