Examination of VLC-PUFA-deficient photoreceptor terminals

• Published in: Investigative ophthalmology & visual science 2014-04, Vol.55 (7), p.4063-4072
• Main Authors: Bennett, Lea D, Hopiavuori, Blake R, Brush, Richard S, Chan, Michael, Van Hook, Matthew J, Thoreson, Wallace B, Anderson, Robert E
• Format: Article
• Language: English
• Subjects: Animals; Blotting, Western; Cattle; Disease Models, Animal; Electroretinography; Eye Proteins - genetics; Eye Proteins - metabolism; Fatty Acids, Unsaturated - deficiency; Lipids - analysis; Macular Degeneration - congenital; Macular Degeneration - genetics; Macular Degeneration - metabolism; Macular Degeneration - pathology; Membrane Proteins - genetics; Membrane Proteins - metabolism; Mice; Mice, Knockout; Microscopy, Electron, Transmission; Mutation; Photoreceptor Cells, Vertebrate - metabolism; Photoreceptor Cells, Vertebrate - ultrastructure; Retina - metabolism; Retina - physiopathology; Retina - ultrastructure; Synaptic Transmission; Synaptosomes - metabolism; Synaptosomes - ultrastructure; Tandem Mass Spectrometry
• ISSN: 1552-5783; 0146-0404; 1552-5783
• DOI: 10.1167/iovs.14-13997

Juvenile-onset autosomal dominant Stargardt-like macular dystrophy (STGD3) is caused by mutations in ELOVL4 (elongation of very long fatty acids-4), an elongase necessary for the biosynthesis of very long chain fatty acids (VLC-FAs ≥ C26). Photoreceptors are enriched with VLC polyunsaturated fatty acids (VLC-PUFAs), which are necessary for long-term survival of rod photoreceptors. The purpose of these studies was to determine the effect of deletion of VLC-PUFAs on rod synaptic function in retinas of mice conditionally depleted (KO) of Elovl4. Retina function was assessed in wild-type (WT) and KO by electroretinography. Outer plexiform structure was evaluated by immunofluorescence and transmission electron microscopy. Single-cell recordings measured rod ion channel operation and rod bipolar glutamate signaling. Sucrose gradient centrifugation was used to isolate synaptosomes from bovine retina. Proteins and lipids were analyzed by Western blotting and tandem mass spectroscopy, respectively. Inner retinal responses (b-wave, oscillatory potentials, and scotopic threshold responses) of the ERG were decreased in the KO mice compared to controls. However the rod ion channel operation and bipolar glutamate responses were comparable between groups. Biochemical analysis revealed that conventional and ribbon synapses have VLC-PUFAs. Ultrastructural analysis showed that the outer plexiform layer was disorganized and the diameter of vesicles in rod terminals was smaller in the KO mice. Very long chain PUFAs affect rod function by contributing to synaptic vesicle size, which may alter the dynamics of synaptic transmission, ultimately resulting in a loss of neuronal connectivity and death of rod photoreceptors.