April 2010
Volume 51, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2010
Role of Amyloid Precursor Protein in Lipoprotein Deposition by Retinal Pigment Epithelium
Author Affiliations & Notes
  • R. Sato
    Ophthalmology and Visual Science, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan
  • T. Yasukawa
    Ophthalmology and Visual Science, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan
  • A. Takase
    Ophthalmology and Visual Science, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan
  • A. Kato
    Ophthalmology and Visual Science, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan
  • A. Nishiwaki
    Ophthalmology and Visual Science, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan
  • P. Wiedemann
    Ophthalmology, Leipzig University, Leipzig, Germany
  • Y. Ogura
    Ophthalmology and Visual Science, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan
  • Footnotes
    Commercial Relationships  R. Sato, None; T. Yasukawa, None; A. Takase, None; A. Kato, None; A. Nishiwaki, None; P. Wiedemann, None; Y. Ogura, None.
  • Footnotes
    Support  2009-2011 Grant-in-Aid for Scientific Research from Japan Society for the Promotion of Science
Investigative Ophthalmology & Visual Science April 2010, Vol.51, 6159. doi:
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      R. Sato, T. Yasukawa, A. Takase, A. Kato, A. Nishiwaki, P. Wiedemann, Y. Ogura; Role of Amyloid Precursor Protein in Lipoprotein Deposition by Retinal Pigment Epithelium. Invest. Ophthalmol. Vis. Sci. 2010;51(13):6159.

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

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Abstract

Purpose: : Amyloid ß is supposed to be associated with pathogenesis of age-related macular degeneration because of the expression of amyloid ß in hard drusen. The aim of this study is to clarify the relationship of amyloid ß expression with physiological functions of retinal pigment epithelium (RPE).

Methods: : Human RPE cells were cultured in medium with methylcellulose on 96-well round bottom culture dish. RPE cells aggregated and formed a spheroid, on the surface of which a monolayer of RPE was constructed. ß-secretase inhibitor or γ-secretase inhibitor was used to inhibit the production of amyloid ß from amyloid precursor protein (APP). At week 1, spheroids were measured in diameter and observed in morphology. Localization of apoB-100 and elastin was evaluated by immunohistochemistry.

Results: : Diameters of spheroids in the group treated with each secretase inhibitor were bigger than those in the control group through the observation period. Outward deposition of lipoproteins in each treatment group was less than that in the control group. Spheroids in each treatment group had smooth surface. ApoB-100, a component of RPE-derived lipoproteins, and elastin, a major element of Bruch’s membrane, were stained in each group treated with secretase inhibitors less intensely than in the control group.

Conclusions: : Amyloid ß inhibitor reduced the production of lipoproteins and the turnover of elastin. These results suggested that cleavage of APP by secretases might play a role in lipoprotein deposition, which might require subsequent reconstruction of Bruch’s membrane.

Keywords: age-related macular degeneration • retinal pigment epithelium • Bruch's membrane 
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