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    Expanded Progenitor Populations, Vitreo-Retinal Abnormalities, and Muller Glial Reactivity in the Zebrafish Leprechaun/Patched2 Retina

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    Date
    2009-10
    Author
    Bibliowicz, Jonathan
    Gross, Jeffrey M.
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    Abstract
    The roles of the Hedgehog (Hh) pathway in controlling vertebrate retinal development have been studied extensively; however, species-and context-dependent findings have provided differing conclusions. Hh signaling has been shown to control both population size and cell cycle kinetics of proliferating retinal progenitors, and to modulate differentiation within the retina by regulating the timing of cell cycle exit. While cell cycle exit has in turn been shown to control cell fate decisions within the retina, a direct role for the Hh pathway in retinal cell fate decisions has yet to be established in vivo. Results: To gain further insight into Hh pathway function in the retina, we have analyzed retinal development in leprechaun/patched2 mutant zebrafish. While lep/ptc2 mutants possessed more cells in their retinas, all cell types, except for Muller glia, were present at identical ratios as those observed in wild-type siblings. lep/ptc2 mutants possessed a localized upregulation of GFAP, a marker for 'reactive' glia, as well as morphological abnormalities at the vitreo-retinal interface, where Muller glial endfeet terminate. In addition, analysis of the over-proliferation phenotype at the ciliary marginal zone (CMZ) revealed that the number of proliferating progenitors, but not the rate of proliferation, was increased in lep/ptc2 mutants. Conclusion: Our results indicate that Patched2-dependent Hh signaling does not likely play an integral role in neuronal cell fate decisions in the zebrafish retina. ptc2 deficiency in zebrafish results in defects at the vitreo-retinal interface and Muller glial reactivity. These phenotypes are similar to the ocular abnormalities observed in human patients suffering from Basal Cell Naevus Syndrome (BCNS), a disorder that has been linked to mutations in the human PTCH gene (the orthologue of the zebrafish ptc2), and point to the utility of the lep/ptc2 mutant line as a model for the study of BCNS-related ocular pathologies. Our findings regarding CMZ progenitor proliferation suggest that, in the zebrafish retina, Hh pathway activity may not affect cell cycle kinetics; rather, it likely regulates the size of the retinal progenitor pool in the CMZ.
    Department
    Cellular and Molecular Biology
    Subject
    cell-cycle exit
    sonic-hedgehog
    danio-rerio
    ciliary margin
    vertebrate
    eye
    ganglion-cells
    human homolog
    gene
    differentiation
    proliferation
    developmental biology
    URI
    http://hdl.handle.net/2152/43202
    Citation
    Bibliowicz, Jonathan, and Jeffrey M. Gross. "Expanded progenitor populations, vitreo-retinal abnormalities, and Müller glial reactivity in the zebrafish leprechaun/patched 2 retina." BMC developmental biology, Vol. 9, No. 1 (Oct., 2009): 1.
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    • facebook
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