Evidence map›Paper›PMID 27096757›Full record

ArticleInvestigative ophthalmology & visual science2016

Antiviral Drug Ganciclovir Is a Potent Inhibitor of the Proliferation of Müller Glia-Derived Progenitors During Zebrafish Retinal Regeneration.

Shuqiang Zhang, Zhaoxia Mu, Chunjiao He, Minmin Zhou, Dong Liu, Xiao-Feng Zhao, Daniel Goldman, Hui Xu

Open access · goldAbstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.5field-weighted citation impact, top 29% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Microglia response and function in a chronic model of photoreceptor damage.Frontiers in cell and developmental biology · 2025
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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

8 authors at 3 institutions in 2 countries.

Shuqiang ZhangJiangsu Key Lab of Neuroregeneration Co-innovation Center of Neuroregeneration, Nantong University, Nantong, Jiangsu Province, China.
Zhaoxia MuEye Institute, Affiliated Hospital of Nantong University, Nantong, Jiangsu Province, China.
Chunjiao HeJiangsu Key Lab of Neuroregeneration Co-innovation Center of Neuroregeneration, Nantong University, Nantong, Jiangsu Province, China.
Minmin ZhouCollege of Biological Science, Nantong University, Nantong, Jiangsu Province, China.
Dong LiuJiangsu Key Lab of Neuroregeneration Co-innovation Center of Neuroregeneration, Nantong University, Nantong, Jiangsu Province, China.
Xiao-Feng ZhaoDepartment of Cell and Developmental Biology, University of Michigan, Ann Arbor, Michigan, United States.
Daniel GoldmanMolecular and Behavioral Neuroscience Institute and Department of Biological Chemistry, University of Michigan, Ann Arbor, Michigan, United States.
Hui XuJiangsu Key Lab of Neuroregeneration Co-innovation Center of Neuroregeneration, Nantong University, Nantong, Jiangsu Province, China.
Nantong University · CNMichigan United · USAffiliated Hospital of Nantong University · CN

Funding

Muller glia and retina regeneration-Diversity supplementR01EY018132 · NEI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GOLDMAN, DANIEL J · 2007 to 2019
$4.8M
NEI NIH HHS R01 EY018132
6 · The paper itself

Abstract

purposeThe purpose of this study was to investigate the effect of the antiviral drug ganciclovir (GCV) on Müller glia dedifferentiation and proliferation and the underlying cellular and molecular mechanisms in adult zebrafish.

methodsA Tg(1016tuba1a:GFP) transgenic line was generated to identify injury-induced dedifferentiation of Müller glia. Mechanical retinal damage was induced by a needle-poke injury on the back of the eyes in adult zebrafish. Phosphate-buffered saline or GCV was injected into the vitreous of the eye at the time of injury or through the cornea. The GCV clearance rate from the eye was determined by a reversed-phase HPLC method. Green fluorescent protein (GFP) and bromodeoxyuridine (BrdU) immunofluorescence were used to determine the effect of GCV on retinal regeneration. Cell apoptosis was evaluated by TUNEL staining. Microglia were labeled by vitreous injection of isolectin IB4 conjugates. Quantitative (q)PCR and Western blot analysis were used to determine gene expression in the retina.

resultsGanciclovir treatment significantly reduced the number of BrdU+ Müller glia-derived progenitor cells (MGPCs) at 4 days post injury. Further analysis showed that GCV had no impact on Müller glia dedifferentiation and the initial formation of MGPCs. Our data indicate that GCV irreversibly inhibited MGPC proliferation likely through a p53-p21(cip1)-dependent pathway. Interestingly, unlike control cells, GCV-treated Müller glia cells were "locked" in a prolonged dedifferentiated state.

conclusionsOur study uncovered a novel inhibitory effect of GCV on MGPC proliferation and suggests its potential use as a tool to uncover molecular mechanisms underlying retinal regeneration in zebrafish.

Indexed as

AnimalsAntiviral AgentsCell DifferentiationCell LineCell ProliferationEpendymoglial CellsFluorescent Antibody TechniqueGanciclovirNeural Stem CellsReal-Time Polymerase Chain ReactionRegenerationRetinaZebrafishAntiviral AgentsGanciclovir

Identifiers

PMID27096757
PMCPMC4849886
OpenAlexW2342068961

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.