Literature DB >> 25152361

Studying melanin and lipofuscin in RPE cell culture models.

Michael E Boulton1.   

Abstract

The retinal pigment epithelium contains three major types of pigment granules; melanosomes, lipofuscin and melanolipofuscin. Melanosomes in the retinal pigment epithelium (RPE) are formed during embryogenesis and mature during early postnatal life while lipofuscin and melanolipofuscin granules accumulate as a function of age. The difficulty in studying the formation and consequences of melanosomes and lipofuscin granules in RPE cell culture is compounded by the fact that these pigment granules do not normally occur in established RPE cell lines and pigment granules are rapidly lost in adult human primary culture. This review will consider options available for overcoming these limitations and permitting the study of melanosomes and lipofuscin in cell culture and will briefly evaluate the advantages and disadvantages of the different protocols.
Copyright © 2014 The Author. Published by Elsevier Ltd.. All rights reserved.

Entities:  

Keywords:  A2E; RPE; cell culture; lipofuscin; melanin; melanosomes

Mesh:

Substances:

Year:  2014        PMID: 25152361      PMCID: PMC4143628          DOI: 10.1016/j.exer.2014.01.016

Source DB:  PubMed          Journal:  Exp Eye Res        ISSN: 0014-4835            Impact factor:   3.467


  75 in total

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6.  Formation of lipofuscin-like material in the RPE Cell by different components of rod outer segments.

Authors:  Lei Lei; Radouil Tzekov; J Hugh McDowell; Wesley C Smith; Shibo Tang; Shalesh Kaushal
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Review 7.  Development of human embryonic stem cell therapies for age-related macular degeneration.

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Authors:  Zsolt Ablonczy; Daniel Higbee; David M Anderson; Mohammad Dahrouj; Angus C Grey; Danielle Gutierrez; Yiannis Koutalos; Kevin L Schey; Anne Hanneken; Rosalie K Crouch
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Review 10.  Autophagy and heterophagy dysregulation leads to retinal pigment epithelium dysfunction and development of age-related macular degeneration.

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  26 in total

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5.  A platform for assessing outer segment fate in primary human fetal RPE cultures.

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6.  Visible light OCT improves imaging through a highly scattering retinal pigment epithelial wall.

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7.  Light induces NLRP3 inflammasome activation in retinal pigment epithelial cells via lipofuscin-mediated photooxidative damage.

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9.  A2E-associated cell death and inflammation in retinal pigmented epithelial cells from human induced pluripotent stem cells.

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