April 2010
Volume 51, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2010
Lack of Opticin in Mice Results in Delayed Hyaloid Vascular Regression and Retinal Vascular Development
Author Affiliations & Notes
  • M. M. Le Goff
    Wellcome Trust Centre for Cell-Matrix Research, Faculty of Life Sciences,
    The Medical School, Faculty of Medical and Human Sciences,
    University of Manchester, Manchester, United Kingdom
  • P. N. Bishop
    Wellcome Trust Centre for Cell-Matrix Research, Faculty of Life Sciences,
    The Medical School, Faculty of Medical and Human Sciences,
    University of Manchester, Manchester, United Kingdom
  • R. Mayne
    Department of Cell Biology, University of Alabama, Birmingham, Alabama
  • M. Ugarte
    The Medical School, Faculty of Medical and Human Sciences,
    University of Manchester, Manchester, United Kingdom
  • Footnotes
    Commercial Relationships  M.M. Le Goff, None; P.N. Bishop, None; R. Mayne, None; M. Ugarte, None.
  • Footnotes
    Support  Support for the NIHR Manchester Biomedical Research Centre
Investigative Ophthalmology & Visual Science April 2010, Vol.51, 25. doi:
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      M. M. Le Goff, P. N. Bishop, R. Mayne, M. Ugarte; Lack of Opticin in Mice Results in Delayed Hyaloid Vascular Regression and Retinal Vascular Development. Invest. Ophthalmol. Vis. Sci. 2010;51(13):25.

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

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Abstract

Purpose: : Nutrients and oxygen necessary for early retinal development are provided by a vascular network of the vitreous called the hyaloid system. As the hyaloid system regresses, the retinal vasculature develops radially from the optic disk. Opticin is a vitreous glycoprotein that has anti-angiogenic properties. In this study, we investigate if a lack of opticin perturbs hyaloid regression and retinal vascular development.

Methods: : Initially, immunohistochemistry was performed on 5 µm eye sections from wild-type and Optc-/- mice at P4, P7 and P17 using an anti-mouse opticin antibody. Subsequently, the hyaloid vessels and retinal vasculature were fluorescently labelled with isolectin B4 in wild-type and Optc-/- eye cups and retinal flat-mounts prepared at P4, P7, P17 and P35 to observe vascular development.

Results: : Opticin was localized to the non-pigmented ciliary epithelium, vitreous, hyaloid vasculature and trabecular meshwork. Fluorescent microscopy revealed a more extensive hyaloid vascularization in the Optc-/- mice at P4 and P7 compared to their wild-type counterparts. While the hyaloid network had totally regressed in the wild-type animals at P35, residual vessels were observed in a proportion of the Optc-/- mice. Analyses of retinal flat-mounts at P4 and P7 revealed a delay in retinal vascularization in Optc-/- compared to wild-type mice; however, no differences were observed in the vascular pattern by P17.

Conclusions: : Opticin is involved in hyaloid regression and indirectly influences the rate of retinal vascularization.

Keywords: vitreous • extracellular matrix • glycoconjugates/glycoproteins 
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