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The role of the photoreceptor ABC transporter ABCA4 in lipid transport and Stargardt macular degeneration
被引:120
|作者:
Molday, Robert S.
[1
]
Zhong, Ming
Quazi, Faraz
机构:
[1] Univ British Columbia, Ctr Macular Res, Dept Biochem & Mol Biol, Vancouver, BC V6T 1Z3, Canada
来源:
基金:
加拿大健康研究院;
关键词:
ABC transporter;
ABCA4;
Stargardt macular degeneration;
Lipid transport;
Photoreceptor;
Visual cycle;
Membrane protein;
Retinal degenerative disease;
ATP-BINDING CASSETTE;
OUTER SEGMENT DISKS;
CONE-ROD DYSTROPHY;
DISEASE GENE ABCR;
FAMILIAL INTRAHEPATIC CHOLESTASIS;
LEBERS CONGENITAL AMAUROSIS;
INTRINSIC MEMBRANE-PROTEIN;
THERAPY RESTORES VISION;
MOUSE MODEL;
FUNDUS FLAVIMACULATUS;
D O I:
10.1016/j.bbalip.2009.02.004
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
ABCA4 is a member of the ABCA subfamily of ATP binding cassette (ABC) transporters that is expressed in rod and cone photoreceptors of the vertebrate retina. ABCA4, also known as the Rim protein and ABCR, is a large 2273 amino acid glycoprotein organized as two tandem halves, each containing a single membrane spanning segment followed sequentially by a large exocytoplasmic domain, a multispanning membrane domain and a nucleotide binding domain. Over 500 mutations in the gene encoding ABCA4 are associated with a spectrum of related autosomal recessive retinal degenerative diseases including Stargardt macular degeneration, cone-rod dystrophy and a subset of retinitis pigmentosa. Biochemical studies on the purified ABCA4 together with analysis of abca4 knockout mice and patients with Stargardt disease have implicated ABCA4 as a retinylidene-phosphatidylethanolamine transporter that facilitates the removal of potentially reactive retinal derivatives from photoreceptors following photoexcitation. Knowledge of the genetic and molecular basis for ABCA4 related retinal degenerative diseases is being used to develop rationale therapeutic treatments for this set of disorders. (C) 2009 Elsevier B.V. All rights reserved.
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页码:573 / 583
页数:11
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