May 2006
Volume 47, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2006
Analysis of Inner Retinal Changes in Eyes of Rpe65–/– Mice Treated With Lentivirus–hRPE65
Author Affiliations & Notes
  • T.S. Rex
    Ophthalmology, University of Pennsylvania, Philadelphia, PA
  • N.S. Dejneka
    Ophthalmology, University of Pennsylvania, Philadelphia, PA
  • E.M. Surace
    Ophthalmology, University of Pennsylvania, Philadelphia, PA
  • A.M. Maguire
    Ophthalmology, University of Pennsylvania, Philadelphia, PA
  • J. Bennett
    Ophthalmology, University of Pennsylvania, Philadelphia, PA
  • Footnotes
    Commercial Relationships  T.S. Rex, None; N.S. Dejneka, None; E.M. Surace, None; A.M. Maguire, None; J. Bennett, None.
  • Footnotes
    Support  RO1 EY10820, U10EY013729, Foundation Fighting Blindness, Research to Prevent Blindness, the Paul and Evanina Mackall Foundation Trust, the F.M. Kirby Foundation
Investigative Ophthalmology & Visual Science May 2006, Vol.47, 850. doi:
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      T.S. Rex, N.S. Dejneka, E.M. Surace, A.M. Maguire, J. Bennett; Analysis of Inner Retinal Changes in Eyes of Rpe65–/– Mice Treated With Lentivirus–hRPE65 . Invest. Ophthalmol. Vis. Sci. 2006;47(13):850.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose: : To analyze morphological changes in the inner retina of adult Rpe65–/– mice. To evaluate the effects of subretinal injection of a therapeutic virus, lentivirus–hRPE65, on these changes.

Methods: : Rpe65–/– mice were treated at age 4 months with subretinal injection of lentivirus–hRPE65. Contralateral eyes were injected with vehicle alone. After 1–2 months animals were euthanized and eyes were processed for histology. Retinal sections from experimental and control eyes were treated with antibodies specific to different inner retinal cells. Additional eyes were also harvested from untreated Rpe65–/– and wildtype C57Bl/6 mice aged 5 months to 2 years. We used anti–calbindin, anti–calretinin, anti–PKC and anti–GFAP to label the horizontal, amacrine, bipolar, and Muller cells, respectively.

Results: : There was an upregulation of GFAP in the Muller cells of al Rpe65–/– retinas, regardless of whether the mice had received subretinal injection. Rod bipolar cell dendrites were also shortened in experimental and untreated retinas.

Conclusions: : Histopathological changes were noted in the inner retina of all Rpe65–/– mice, regardless of whether the eyes had been treated with injection of lentivirus–hRPE65. The significance of these changes in unknown. Further studies will determine what impact these changes have on visual function.

Keywords: gene transfer/gene therapy • immunohistochemistry • retina 
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