May 2004
Volume 45, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2004
Alkylphosphocholines inhibit human RPE cell adhesion and migration
Author Affiliations & Notes
  • K.H. Eibl
    Ophthalmology, LMU Munich, Munich, Germany
  • D. Kook
    Ophthalmology, LMU Munich, Munich, Germany
  • A. Ohlmann
    Ophthalmology, LMU Munich, Munich, Germany
  • A. Wolf
    Ophthalmology, LMU Munich, Munich, Germany
  • S. Priglinger
    Ophthalmology, LMU Munich, Munich, Germany
  • A. Kampik
    Ophthalmology, LMU Munich, Munich, Germany
  • U. Welge–Luessen
    Ophthalmology, LMU Munich, Munich, Germany
  • Footnotes
    Commercial Relationships  K.H. Eibl, None; D. Kook, None; A. Ohlmann, None; A. Wolf, None; S. Priglinger, None; A. Kampik, None; U. Welge–Luessen, None.
  • Footnotes
    Support  none
Investigative Ophthalmology & Visual Science May 2004, Vol.45, 3194. doi:
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      K.H. Eibl, D. Kook, A. Ohlmann, A. Wolf, S. Priglinger, A. Kampik, U. Welge–Luessen; Alkylphosphocholines inhibit human RPE cell adhesion and migration . Invest. Ophthalmol. Vis. Sci. 2004;45(13):3194.

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

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Abstract

Abstract: : Purpose: To determine the effect of alkylphosphocholines (APCs) on human retinal pigment epithelium (RPE) cell adhesion and migration in vitro. Methods: Cultured RPE cells of five human donors were treated with four different APCs in the presence of fetal calf serum at non–toxic concentrations as determined previously by a trypan blue exclusion assay. Adhesion on collagen and fibronectin coated 24–well dishes was assessed by inverse centrifugation of the culture dishes followed by a tetrazolium dye–reduction assay (MTT) at 550 nm. Migration was assessed by a modification of the Boyden chamber method with PEDF in the lower part of the chamber. Migrated RPE cells were stained with hematoxylin–eosin, viewed under a phase–contract microscope and counted. Results: All four APCs were able to inhibit RPE cell adhesion below 40% on collagen and below 35% on fibronectin at 1500 rpm. RPE migration was reduced by more than 80% for all APCs applied. Trypan blue staining revealed a toxicity below 5 % within the concentration interval tested. Conclusions: All APCs inhibited RPE cell adhesion and migration at non–toxic concentrations in vitro. This might be a novel approach for prevention of RPE–mediated proliferative processes such as PVR.

Keywords: proliferative vitreoretinopathy • retinal pigment epithelium • pharmacology 
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