Please use this identifier to cite or link to this item: https://doi.org/10.1074/jbc.M116.721340
Title: Mfsd2a Is a Transporter for the Essential omega-3 Fatty Acid Docosahexaenoic Acid (DHA) in Eye and Is Important for Photoreceptor Cell Development
Authors: Wong, Bernice H 
Chan, Jia Pei 
Cazenave-Gassiot, Amaury 
Poh, Rebecca W
Foo, Juat Chin 
Galam, Dwight LA 
Ghosh, Sujoy 
Nguyen, Long N 
Barathi, Veluchamy A
Yeo, Sia W
Luu, Chi D
Wenk, Markus R 
Silver, David L
Keywords: Science & Technology
Life Sciences & Biomedicine
Biochemistry & Molecular Biology
RETINAL-PIGMENT EPITHELIUM
BRAIN
EXPRESSION
PHAGOCYTOSIS
PERICYTES
DISEASE
ORGANIZATION
CLONING
HEALTH
VEGF
Issue Date: 13-May-2016
Publisher: AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
Citation: Wong, Bernice H, Chan, Jia Pei, Cazenave-Gassiot, Amaury, Poh, Rebecca W, Foo, Juat Chin, Galam, Dwight LA, Ghosh, Sujoy, Nguyen, Long N, Barathi, Veluchamy A, Yeo, Sia W, Luu, Chi D, Wenk, Markus R, Silver, David L (2016-05-13). Mfsd2a Is a Transporter for the Essential omega-3 Fatty Acid Docosahexaenoic Acid (DHA) in Eye and Is Important for Photoreceptor Cell Development. JOURNAL OF BIOLOGICAL CHEMISTRY 291 (20) : 10501-10514. ScholarBank@NUS Repository. https://doi.org/10.1074/jbc.M116.721340
Abstract: © 2016 by The American Society for Biochemistry and Molecular Biology, Inc. Published in the U.S.A. Eye photoreceptor membrane discs in outer rod segments are highly enriched in the visual pigment rhodopsin and the ω-3 fatty acid docosahexaenoic acid (DHA). The eye acquires DHA from blood, but transporters for DHA uptake across the bloodretinal barrier or retinal pigment epithelium have not been identified. Mfsd2a is a newly described sodium-dependent lysophosphatidylcholine (LPC) symporter expressed at the bloodbrain barrier that transports LPCs containing DHA and other long-chain fatty acids. LPC transport via Mfsd2a has been shown to be necessary for human brain growth. Here we demonstrate that Mfsd2a is highly expressed in retinal pigment epithelium in embryonic eye, before the development of photoreceptors, and is the primary site of Mfsd2a expression in the eye. Eyes from whole body Mfsd2a-deficient (KO) mice, but not endothelium-specific Mfsd2a-deficient mice, were DHA-deficient and had significantly reduced LPC/DHA transport in vivo. Fluorescein angiography indicated normal blood-retinal barrier function. Histological and electron microscopic analysis indicated that Mfsd2a KO mice exhibited a specific reduction in outer rod segment length, disorganized outer rod segment discs, and mislocalization of and reduction in rhodopsin early in postnatal development without loss of photoreceptors. Minor photoreceptor cell loss occurred in adult Mfsd2a KO mice, but electroretinography indicated visual function was normal. The developing eyes of Mfsd2aKOmice had activated microglia and up-regulation of lipogenic and cholesterogenic genes, likely adaptations to loss of LPC transport. These findings identify LPC transport via Mfsd2a as an important pathway for DHA uptake in eye and for development of photoreceptor membrane discs.
Source Title: JOURNAL OF BIOLOGICAL CHEMISTRY
URI: https://scholarbank.nus.edu.sg/handle/10635/170476
ISSN: 00219258
1083351X
DOI: 10.1074/jbc.M116.721340
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