generating-retinal-injury-models-in-xenopus-tadpoles

Generating Retinal Injury Models in <em>Xenopus</em> Tadpoles

Retinal neurodegenerative diseases are the leading causes of blindness. Among numerous therapeutic strategies being explored, stimulating self-repair ...

Université Paris-Saclay

Retinitis pigmentosa is an inherited retinal dystrophy that ultimately leads to blindness due to the progressive degeneration of rod photoreceptors and the subsequent non-cell autonomous death of cones.  is the most frequently mutated gene in this disease. We here developed  gene editing-based models of retinitis pigmentosa in two  species,  and , by using CRISPR/Cas9 technology. In both of them, loss of  function results in massive rod cell degeneration characterized by progressive shortening of outer segments and occasional cell death. This is followed by cone morphology deterioration. Despite these apparently similar degenerative environments, we found that Müller glial cells behave differently in  and . While a significant proportion of Müller cells re-enter into the cell cycle in , their proliferation remains extremely limited in . This work thus reveals divergent responses to retinal injury in closely related species. These models should help in the future to deepen our understanding of the mechanisms that have shaped regeneration during evolution, with tremendous differences across vertebrates.

Alicia Donval

Paris-Saclay Institute of Neuroscience,
CNRS,
Paris-Saclay Institute of Neuroscience, CNRS

Université Paris-Saclay

Generating Retinal Injury Models in Xenopus Tadpoles

Alicia Donval

Paris-Saclay Institute of Neuroscience,CNRS,Paris-Saclay Institute of Neuroscience, CNRS

Université Paris-Saclay

Generating Retinal Injury Models in Xenopus Tadpoles

Paris-Saclay Institute of Neuroscience,
CNRS,
Paris-Saclay Institute of Neuroscience, CNRS