Inner retinal abnormalities in a mouse model of Leber's congenital amaurosis

Authors

  • Vincenzo Pignatelli,

    1. Istituto di Neuroscienze del Consiglio Nazionale delle Ricerche (CNR), Laboratorio di Neurofisiologia, Area della Ricerca CNR, 56100 Pisa, Italy
    Search for more papers by this author
  • Constance Louise Cepko,

    1. Department of Genetics and Howard Hughes Medical Institute, Harvard Medical School, Boston, Massachusetts 02115
    Search for more papers by this author
  • Enrica Strettoi

    Corresponding author
    1. Istituto di Neuroscienze del Consiglio Nazionale delle Ricerche (CNR), Laboratorio di Neurofisiologia, Area della Ricerca CNR, 56100 Pisa, Italy
    • Istituto di Neuroscienze del CNR, Laboratorio di Neurofisiologia, Area della Ricerca, Via G. Moruzzi 1, 56100 Pisa, Italy
    Search for more papers by this author

Abstract

Leber's congenital amaurosis (LCA) is the earliest and most severe form in the world of genetic retinal dystrophy causing blindness. An animal model of LCA was recently created in which the cone-rod homeobox (crx) gene was disrupted using homologous recombination. Crx−/− mice display abnormal development of photoreceptors followed by their degeneration. We analyzed the morphology of inner retinal cells in crx−/− mice in order to evaluate the effects of abnormal photoreceptor development and death upon other retinal neurons. The identification of a time window during which inner retinal cells are still viable could be very important in view of the possibilities that photoreceptor transplantation or gene therapy might be used to restore vision in LCA. We used a combination of immunocytochemical and confocal microscopy techniques to screen the crx−/− inner retina and verify its morphological integrity after photoreceptor degeneration. We found significant morphological alterations in second-order neurons in crx−/− animals. The appearance of mutant retinas after photoreceptor death is indistinguishable from that of the retinal degeneration (rd/rd) mouse, a different genetic model of a retinal disease characterized by photoreceptor degeneration. However, at early stages of photoreceptor degeneration the morphology of retinal cells in the crx−/− mutant is considerably well preserved. It is likely that different genetic mechanisms that cause abnormal photoreceptor development and/or degeneration lead to a common pathway that determines second-order neuron modifications. The severity of modifications is linked to the timing of onset of the degeneration and appears to increase with time. J. Comp. Neurol. 469:351–359, 2004. © 2004 Wiley-Liss, Inc.

Ancillary