Deposition of a fluorophoric material, known as lipofuscin, in retinal pigment epithelium cells has been speculated to be one of the biomarkers of age-related macular degeneration. One of the fluorophores of lipofuscin has been characterized as A2E, a pyridinium bisretinoid. Its cationic nature along with two hydrophobic retinal chains suggests that it can disrupt the membrane integrity by its detergent-like activity and can thus cause cellular damage. With this notion, we studied in detail the interaction between A2E and the model membranes of different lipid compositions using fluorescence steady-state and fluorescence anisotropy measurements. A transition from vesicular to micellar structure occurred upon incorporation of A2E into the lipid bilayer. However, the A2E concentration at which this transition occurred depends on the lipid composition. A lipid mixture containing 10% phosphatidylserine (PS) (close to disc membrane PS content) behaved similarly to a lipid mixture having no PS. In contrast, vesicles containing 20% PS showed significantly different behavior. Membrane solubilization by A2E was also confirmed by vesicle leakage experiments. A2E also showed significant activity in liposome-mediated gene transfection. A lipid formulation containing 40% A2E and a helper lipid showed plasmid DNA transfection efficiency comparable to commercially available transfection reagents with no evidence of cytotoxicity. These results contribute to understanding the mechanism underlying the A2E-induced cellular dysfunction.
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1 August 2002
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July 30 2002
Interaction of A2E with Model Membranes. Implications to the Pathogenesis of Age-related Macular Degeneration
Soma De,
Soma De
Howard Hughes Medical Institute, Laboratory of Molecular Biology and Biochemistry, The Rockefeller University, New York, NY 10021
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Thomas P. Sakmar
Thomas P. Sakmar
Howard Hughes Medical Institute, Laboratory of Molecular Biology and Biochemistry, The Rockefeller University, New York, NY 10021
Search for other works by this author on:
Soma De
Howard Hughes Medical Institute, Laboratory of Molecular Biology and Biochemistry, The Rockefeller University, New York, NY 10021
Thomas P. Sakmar
Howard Hughes Medical Institute, Laboratory of Molecular Biology and Biochemistry, The Rockefeller University, New York, NY 10021
Address correspondence to Thomas P. Sakmar, Box 284, Rockefeller University, 1230 York Ave., New York, NY 10021. Fax (212) 327-7904; E-mail: [email protected]
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Abbreviations used in this paper: AMD, age-related macular degeneration; DOPC, 1,2-dioleoyl-sn-glycero-3-phosphocholine; DOPE, 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine; DOPS, 1,2-dioleoyl-sn-glycero-3-[phospho-L-serine] (sodium salt); DPH, 1,6-diphenyl-1,3,5-hexatriene; LUV, large unilamellar vesicles; ROS, rod outer segment; RPE, retinal pigment epithelium; SUV, small unilamellar vesicle.
Received:
January 22 2002
Revision Received:
May 06 2002
Accepted:
May 29 2002
Online ISSN: 1540-7748
Print ISSN: 0022-1295
The Rockefeller University Press
2002
J Gen Physiol (2002) 120 (2): 147–157.
Article history
Received:
January 22 2002
Revision Received:
May 06 2002
Accepted:
May 29 2002
Citation
Soma De, Thomas P. Sakmar; Interaction of A2E with Model Membranes. Implications to the Pathogenesis of Age-related Macular Degeneration . J Gen Physiol 1 August 2002; 120 (2): 147–157. doi: https://doi.org/10.1085/jgp.20028566
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