March 2012
Volume 53, Issue 14
Free
ARVO Annual Meeting Abstract  |   March 2012
Opticin Suppresses Preretinal Neovascularization, But Does Not Influence Vascular Development In The Murine Eye
Author Affiliations & Notes
  • Paul N. Bishop
    School of Biomedicine, University of Manchester, Manchester, United Kingdom
  • Marta Ugarte
    School of Biomedicine, University of Manchester, Manchester, United Kingdom
  • Hongbin Lu
    School of Biomedicine, University of Manchester, Manchester, United Kingdom
  • Shephen Henry
    M.D. Anderson Cancer Centre, Houston, Texas
  • Masamine Takanosu
    Department of Cell Biology, University of Alabama, Birmingham, Alabama
  • Richard Mayne
    Department of Cell Biology, University of Alabama, Birmingham, Alabama
  • Magali M. Le Goff
    School of Biomedicine, University of Manchester, Manchester, United Kingdom
  • Footnotes
    Commercial Relationships  Paul N. Bishop, Patents US 7910567 B2. and US 7,358,224 B2 (P); Marta Ugarte, None; Hongbin Lu, None; Shephen Henry, None; Masamine Takanosu, None; Richard Mayne, None; Magali M. Le Goff, None
  • Footnotes
    Support  The Wellcome Trust (Grant 057940); NIH Grant R37 AR30481; Manchester NIHR Biomedical Research Centre
Investigative Ophthalmology & Visual Science March 2012, Vol.53, 2545. doi:
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      Paul N. Bishop, Marta Ugarte, Hongbin Lu, Shephen Henry, Masamine Takanosu, Richard Mayne, Magali M. Le Goff; Opticin Suppresses Preretinal Neovascularization, But Does Not Influence Vascular Development In The Murine Eye. Invest. Ophthalmol. Vis. Sci. 2012;53(14):2545.

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

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Abstract

Purpose: : To investigate whether a lack of the extracellular matrix glycoprotein opticin affects retinal vascular development or pathological angiogenesis in the eye.

Methods: : In these experiments opticin null and wild-type mice were compared. The hyaloid vasculature was quantified at P0 and P4 by analysing serial sections through the entire globe. Retinal vascular development at P4 and P7 was analysed by fluorescently-labeling the vasculature in flat mounts. The oxygen-induced retinopathy model was used to assess the effects of a lack of opticin on ischaemia-induced retinal vascular changes and preretinal neovascularization; the results were quantified using SWIFT_NV software.

Results: : Analyses of the hyaloid and retinal vasculature showed that a lack of opticin had no effect on hyaloid vascular regression or development of the retinal vasculature. However, using the oxygen-induced retinopathy model, we demonstrated that opticin knockout mice had decreased retinal vascular pruning at P12, although there were no differences in the hyaloid vasculature at this time point, but increased preretinal neovascularization at P17 compared to wild-type mice.

Conclusions: : A lack of opticin does not influence vascular development, but opticin is anti-angiogenic and inhibits preretinal neovascularization.

Keywords: neovascularization • extracellular matrix • development 
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