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Subretinal Pigment Epithelial Deposition of Drusen Components Including Hydroxyapatite in a Primary Cell Culture Model

PURPOSE: Extracellular deposits containing hydroxyapatite, lipids, proteins, and trace metals that form between the basal lamina of the RPE and the inner collagenous layer of Bruch's membrane are hallmarks of early AMD. We examined whether cultured RPE cells could produce extracellular deposits...

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Autores principales: Pilgrim, Matthew G., Lengyel, Imre, Lanzirotti, Antonio, Newville, Matt, Fearn, Sarah, Emri, Eszter, Knowles, Jonathan C., Messinger, Jeffrey D., Read, Russell W., Guidry, Clyde, Curcio, Christine A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5295770/
https://www.ncbi.nlm.nih.gov/pubmed/28146236
http://dx.doi.org/10.1167/iovs.16-21060
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author Pilgrim, Matthew G.
Lengyel, Imre
Lanzirotti, Antonio
Newville, Matt
Fearn, Sarah
Emri, Eszter
Knowles, Jonathan C.
Messinger, Jeffrey D.
Read, Russell W.
Guidry, Clyde
Curcio, Christine A.
author_facet Pilgrim, Matthew G.
Lengyel, Imre
Lanzirotti, Antonio
Newville, Matt
Fearn, Sarah
Emri, Eszter
Knowles, Jonathan C.
Messinger, Jeffrey D.
Read, Russell W.
Guidry, Clyde
Curcio, Christine A.
author_sort Pilgrim, Matthew G.
collection PubMed
description PURPOSE: Extracellular deposits containing hydroxyapatite, lipids, proteins, and trace metals that form between the basal lamina of the RPE and the inner collagenous layer of Bruch's membrane are hallmarks of early AMD. We examined whether cultured RPE cells could produce extracellular deposits containing all of these molecular components. METHODS: Retinal pigment epithelium cells isolated from freshly enucleated porcine eyes were cultured on Transwell membranes for up to 6 months. Deposit composition and structure were characterized using light, fluorescence, and electron microscopy; synchrotron x-ray diffraction and x-ray fluorescence; secondary ion mass spectroscopy; and immunohistochemistry. RESULTS: Apparently functional primary RPE cells, when cultured on 10-μm-thick inserts with 0.4-μm-diameter pores, can produce sub-RPE deposits that contain hydroxyapatite, lipids, proteins, and trace elements, without outer segment supplementation, by 12 weeks. CONCLUSIONS: The data suggest that sub-RPE deposit formation is initiated, and probably regulated, by the RPE, as well as the loss of permeability of the Bruch's membrane and choriocapillaris complex associated with age and early AMD. This cell culture model of early AMD lesions provides a novel system for testing new therapeutic interventions against sub-RPE deposit formation, an event occurring well in advance of the onset of vision loss.
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spelling pubmed-52957702017-02-08 Subretinal Pigment Epithelial Deposition of Drusen Components Including Hydroxyapatite in a Primary Cell Culture Model Pilgrim, Matthew G. Lengyel, Imre Lanzirotti, Antonio Newville, Matt Fearn, Sarah Emri, Eszter Knowles, Jonathan C. Messinger, Jeffrey D. Read, Russell W. Guidry, Clyde Curcio, Christine A. Invest Ophthalmol Vis Sci Retinal Cell Biology PURPOSE: Extracellular deposits containing hydroxyapatite, lipids, proteins, and trace metals that form between the basal lamina of the RPE and the inner collagenous layer of Bruch's membrane are hallmarks of early AMD. We examined whether cultured RPE cells could produce extracellular deposits containing all of these molecular components. METHODS: Retinal pigment epithelium cells isolated from freshly enucleated porcine eyes were cultured on Transwell membranes for up to 6 months. Deposit composition and structure were characterized using light, fluorescence, and electron microscopy; synchrotron x-ray diffraction and x-ray fluorescence; secondary ion mass spectroscopy; and immunohistochemistry. RESULTS: Apparently functional primary RPE cells, when cultured on 10-μm-thick inserts with 0.4-μm-diameter pores, can produce sub-RPE deposits that contain hydroxyapatite, lipids, proteins, and trace elements, without outer segment supplementation, by 12 weeks. CONCLUSIONS: The data suggest that sub-RPE deposit formation is initiated, and probably regulated, by the RPE, as well as the loss of permeability of the Bruch's membrane and choriocapillaris complex associated with age and early AMD. This cell culture model of early AMD lesions provides a novel system for testing new therapeutic interventions against sub-RPE deposit formation, an event occurring well in advance of the onset of vision loss. The Association for Research in Vision and Ophthalmology 2017-02-01 2017-02 /pmc/articles/PMC5295770/ /pubmed/28146236 http://dx.doi.org/10.1167/iovs.16-21060 Text en Copyright 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
spellingShingle Retinal Cell Biology
Pilgrim, Matthew G.
Lengyel, Imre
Lanzirotti, Antonio
Newville, Matt
Fearn, Sarah
Emri, Eszter
Knowles, Jonathan C.
Messinger, Jeffrey D.
Read, Russell W.
Guidry, Clyde
Curcio, Christine A.
Subretinal Pigment Epithelial Deposition of Drusen Components Including Hydroxyapatite in a Primary Cell Culture Model
title Subretinal Pigment Epithelial Deposition of Drusen Components Including Hydroxyapatite in a Primary Cell Culture Model
title_full Subretinal Pigment Epithelial Deposition of Drusen Components Including Hydroxyapatite in a Primary Cell Culture Model
title_fullStr Subretinal Pigment Epithelial Deposition of Drusen Components Including Hydroxyapatite in a Primary Cell Culture Model
title_full_unstemmed Subretinal Pigment Epithelial Deposition of Drusen Components Including Hydroxyapatite in a Primary Cell Culture Model
title_short Subretinal Pigment Epithelial Deposition of Drusen Components Including Hydroxyapatite in a Primary Cell Culture Model
title_sort subretinal pigment epithelial deposition of drusen components including hydroxyapatite in a primary cell culture model
topic Retinal Cell Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5295770/
https://www.ncbi.nlm.nih.gov/pubmed/28146236
http://dx.doi.org/10.1167/iovs.16-21060
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