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

Zhang, S., Mu, Z., He, C., Zhou, M., Liu, D., Zhao, X.F., Goldman, D., Xu, H.
Investigative ophthalmology & visual science   57: 1991-2000 (Journal)
Registered Authors
Goldman, Dan, Xu, Hui
MeSH Terms
  • Animals
  • Antiviral Agents/pharmacology*
  • Cell Differentiation/drug effects
  • Cell Differentiation/physiology
  • Cell Line
  • Cell Proliferation/drug effects
  • Ependymoglial Cells/drug effects*
  • Ependymoglial Cells/physiology
  • Fluorescent Antibody Technique
  • Ganciclovir/pharmacology*
  • Neural Stem Cells/drug effects*
  • Neural Stem Cells/physiology
  • Real-Time Polymerase Chain Reaction
  • Regeneration/drug effects*
  • Retina/drug effects
  • Retina/growth & development*
  • Zebrafish
27096757 Full text @ Invest. Ophthalmol. Vis. Sci.
The 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.
A 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.
Ganciclovir 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-p21cip1-dependent pathway. Interestingly, unlike control cells, GCV-treated Müller glia cells were "locked" in a prolonged dedifferentiated state.
Our 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.
Genes / Markers
Mutation and Transgenics
Human Disease / Model Data
Sequence Targeting Reagents
Engineered Foreign Genes
Errata and Notes