April 2011
Volume 52, Issue 14
Free
ARVO Annual Meeting Abstract  |   April 2011
Conditional Ablation of Retinal Elovl4 Reveals a Key Role in Synthesis of VLC-PUFAs and Photoreceptor Light Responses
Author Affiliations & Notes
  • Peter Barabas
    Department of Ophthalmology, University of Utah, Salt Lake City, Utah
  • Aihua Liu
    Department of Ophthalmology, University of Utah, Salt Lake City, Utah
  • Wei Xing
    Department of Ophthalmology, University of Utah, Salt Lake City, Utah
  • ZongZhong Tong
    Department of Ophthalmology, University of Utah, Salt Lake City, Utah
  • Yun-Zheng Le
    Medicine, Univ of Oklahoma Hlth Sci Ctr, Oklahoma City, Oklahoma
  • Robert Anderson
    Medicine, Univ of Oklahoma Hlth Sci Ctr, Oklahoma City, Oklahoma
  • Kang Zhang
    Department of Ophthalmology, University of Utah, Salt Lake City, Utah
  • Paul S. Bernstein
    Department of Ophthalmology, University of Utah, Salt Lake City, Utah
  • David Krizaj
    Department of Ophthalmology, University of Utah, Salt Lake City, Utah
  • Footnotes
    Commercial Relationships  Peter Barabas, None; Aihua Liu, None; Wei Xing, None; ZongZhong Tong, None; Yun-Zheng Le, None; Robert Anderson, None; Kang Zhang, None; Paul S. Bernstein, None; David Krizaj, None
  • Footnotes
    Support  NIH Grant EY13870 and P30EY014800, Moran TIGER Award, IRRF Kelman Award, Foundation Fighting Blindness Award, unrestricted grant from RPB to the Moran Eye Center, University of Utah
Investigative Ophthalmology & Visual Science April 2011, Vol.52, 2361. doi:
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      Peter Barabas, Aihua Liu, Wei Xing, ZongZhong Tong, Yun-Zheng Le, Robert Anderson, Kang Zhang, Paul S. Bernstein, David Krizaj; Conditional Ablation of Retinal Elovl4 Reveals a Key Role in Synthesis of VLC-PUFAs and Photoreceptor Light Responses. Invest. Ophthalmol. Vis. Sci. 2011;52(14):2361.

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

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Abstract 
 
Purpose:
 

To compare biochemical, physiological and behavioral phenotypes incurred by the genetic ablation of the Elovl4 elongase and by Elovl4 mutations that impair trafficking of the Elovl4 protein in the transgenic mouse model for autosomal dominant Stargardt disease type 3 (STGD3).

 
Methods:
 

Rod and cone conditional knockout (cKO) mice were generated using the pLox/Cre system. WT1 and TG2 lines carried the human wild type or the human mutant allele (delAACTT at 790-794) in two copies, respectively. RT-PCR and IHC were used to characterize expression and localization of Cre recombinase and Elovl4. Visual acuity and outer retinal physiology were assessed using the optomotor head tracking response and electroretinographic (ERG) analysis, respectively. Gas chromatography coupled with mass spectrometry (GC-MS) was used to determine retinal levels of docosahexaenoic acid (DHA), eicosapentaenoic acid (EPA) and C24-C34 very long chain polyunsaturated fatty acids (VLC-PUFAs).

 
Results:
 

DHA and C24 lipid content of rod cKO retinas did not change whereas there was a ~ 50% decrease in C30-C34 VLC-PUFAs. In contrast, a 43.3% decrease in DHA and 66.5% decrease in C24:5n3 content was measured in TG2 retinas together with undetectable content of C30-C34 VLC-PUFAs. TG2 mice showed a severe visual phenotype with visual acuity that decreased from 0.380±0.006 cyc/deg at 1 month to 0.046±0.030 cyc/deg at 7 months of age. In cone cKO mice, the photopic ERG a- and b-wave decreased by 42.6±11.8% and by 19.2±2.3%, respectively. No ERG changes were observed in rod cKO animals.

 
Conclusions:
 

Our data shows that Elovl4, expressed in rod photoreceptors, is required for synthesis of retinal VLC-PUFAs in the C30-C34 range, but is not required for biosynthesis of C20, C24 lipids. Elovl4 elimination from cones compromised the photopic ERG. The phenotype of transgenic mice carrying the human mutant allele was markedly more severe than the phenotype of mice lacking the Elovl4 protein. We conclude that cone but not rod, retinal signaling is impaired by loss of Elovl4. Moreover, STGD3 may be associated with wider loss of PUFAs and vision loss than expected from a simple loss of Elovl4 protein.

 
Keywords: lipids • retinal degenerations: hereditary • proteins encoded by disease genes 
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