Literature DB >> 19373231

A protocol for the culture and differentiation of highly polarized human retinal pigment epithelial cells.

Shozo Sonoda1, Christine Spee, Ernesto Barron, Stephen J Ryan, Ram Kannan, David R Hinton.   

Abstract

We provide our detailed, standardized in vitro protocol for the culture and differentiation of human retinal pigment epithelial (RPE) cells into a highly polarized and functional monolayer. Disruption of the polarized RPE function plays an important role in the pathogenesis of common blinding disorders of the retina. The availability of this polarized RPE monolayer allows for reproducible evaluation of RPE function, modeling of RPE dysfunction in retinal disease and in vitro evaluation of new therapies. The protocol, which takes approximately 6 weeks to complete, describes the culture of RPE from human fetal donor eyes, the differentiation of these cells into a polarized monolayer with high transepithelial resistance and morphologic characteristics that mimic the RPE monolayer in vivo. By modifying the procedure for initial isolation of pure RPE cells and the culture conditions used in existing protocols, we have established a standardized protocol that provides highly reproducible RPE monolayers from the same donor eye.

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Year:  2009        PMID: 19373231      PMCID: PMC2688697          DOI: 10.1038/nprot.2009.33

Source DB:  PubMed          Journal:  Nat Protoc        ISSN: 1750-2799            Impact factor:   13.491


  29 in total

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  127 in total

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7.  Identification of a novel sodium-coupled oligopeptide transporter (SOPT2) in mouse and human retinal pigment epithelial cells.

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8.  Sonoporation enhances chemotherapeutic efficacy in retinoblastoma cells in vitro.

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9.  Ceramide inhibits connective tissue growth factor expression by human retinal pigment epithelial cells.

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10.  TGF-β2 secretion from RPE decreases with polarization and becomes apically oriented.

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