Literature DB >> 8187832

Superoxide inhibits proliferation and phagocytic internalization of photoreceptor outer segments by bovine retinal pigment epithelium in vitro.

F Becquet1, O Goureau, G Soubrane, G Coscas, Y Courtois, D Hicks.   

Abstract

Experiments were performed to investigate the effect of free radical damage on two aspects of retinal pigmented epithelium (RPE) metabolism, namely, proliferation and phagocytosis. Bovine RPE cells were maintained in monolayer cultures, either as passaged (for proliferation and lysosomal activity assays) or primary cultures (for phagocytosis measurements). Free radicals (superoxide anions) were generated by a xanthine oxidase (XO)-hypoxanthine (HX) reaction. Total phagocytosis (binding plus ingestion of rod outer segments (ROS)) was quantitated by radioimmunoassay using a specific anti-opsin antibody and iodinated secondary antibody. In some cases, agents with known or possible protective influences against oxidative damage, i.e., superoxide dismutase (SOD), vitamin E, and basic fibroblast growth factor (bFGF), were tested for their activity in this model system. RPE cell proliferation was inhibited in a HX-XO dose-dependent manner, in the absence of cell toxicity. Modifications of cell morphology were also noticed. Either simultaneous exposure of RPE cells to ROS membranes and HX-XO or pretreatment of ROS membranes with HX-XO prior to their addition to RPE monolayers led to a statistically significant 20-30% decrease in phagocytosis relative to control values. This decrease was essentially observed in the binding phase of phagocytosis, indicating damage to ROS surface molecules as the primary event. Addition of SOD or vitamin E prevented this loss of phagocytic activity, whereas bFGF had no effect. Superoxide radicals did not, however, affect phagocytosis when RPE cells were exposed to them alone, prior to incubation with ROS; nor did they alter a later stage in the phagocytic process, acid phosphatase activity. This tissue culture model represents a convenient system for analyzing free radical damage in different aspects of RPE-photoreceptor behavior and may be useful in studying this phenomenon in several retinal disorders.

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Year:  1994        PMID: 8187832     DOI: 10.1006/excr.1994.1157

Source DB:  PubMed          Journal:  Exp Cell Res        ISSN: 0014-4827            Impact factor:   3.905


  5 in total

1.  Influence of oxygen free radicals and free radical scavengers on the growth behaviour and oxidative tissue damage of bovine retinal pigment epithelium cells in vitro.

Authors:  A J Augustin; S Hunt; W Breipohl; T Böker; M Spitznas
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1996-01       Impact factor: 3.117

2.  Retinal pigment epithelial acid lipase activity and lipoprotein receptors: effects of dietary omega-3 fatty acids.

Authors:  Victor M Elner
Journal:  Trans Am Ophthalmol Soc       Date:  2002

3.  Cell culture conditions affect RPE phagocytic function.

Authors:  Mike O Karl; Monika Valtink; Jürgen Bednarz; Katrin Engelmann
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2006-12-20       Impact factor: 3.535

4.  miR-17-3p Exacerbates Oxidative Damage in Human Retinal Pigment Epithelial Cells.

Authors:  Bo Tian; Daniel E Maidana; Bernard Dib; John B Miller; Peggy Bouzika; Joan W Miller; Demetrios G Vavvas; Haijiang Lin
Journal:  PLoS One       Date:  2016-08-09       Impact factor: 3.240

5.  Ultrastructural alterations in the retinal pigment epithelium and photoreceptors of a Stargardt patient and three Stargardt mouse models: indication for the central role of RPE melanin in oxidative stress.

Authors:  Tatjana Taubitz; Alexander V Tschulakow; Marina Tikhonovich; Barbara Illing; Yuan Fang; Antje Biesemeier; Sylvie Julien-Schraermeyer; Ulrich Schraermeyer
Journal:  PeerJ       Date:  2018-07-19       Impact factor: 2.984

  5 in total

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