June 2022
Volume 63, Issue 7
Open Access
ARVO Annual Meeting Abstract  |   June 2022
Ablation of pigment epithelium-derived factor receptor, PEDF-R, causes photoreceptor degeneration Alexandra Bernardo-Colón1, Lijin Dong2, Mones Abu-Asab3, and S. Patricia Becerra1 1. Section of Protein Structure and Function, LRCMB; 2. Genetic Engineering Core; 3. Section of Histopathology, NEI-NIH
Author Affiliations & Notes
  • Alexandra Bernardo- Colón
    National Eye Institute, Bethesda, Maryland, United States
  • Ligin Dong
    National Eye Institute, Bethesda, Maryland, United States
  • Mones Abu-Asab
    National Eye Institute, Bethesda, Maryland, United States
  • S Patricia Becerra
    National Eye Institute, Bethesda, Maryland, United States
  • Footnotes
    Commercial Relationships   Alexandra Bernardo- Colón None; Ligin Dong None; Mones Abu-Asab None; S Patricia Becerra None
  • Footnotes
    Support  Intramural Research Program of the NEI
Investigative Ophthalmology & Visual Science June 2022, Vol.63, 1787 – F0336. doi:
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      Alexandra Bernardo- Colón, Ligin Dong, Mones Abu-Asab, S Patricia Becerra; Ablation of pigment epithelium-derived factor receptor, PEDF-R, causes photoreceptor degeneration Alexandra Bernardo-Colón1, Lijin Dong2, Mones Abu-Asab3, and S. Patricia Becerra1 1. Section of Protein Structure and Function, LRCMB; 2. Genetic Engineering Core; 3. Section of Histopathology, NEI-NIH. Invest. Ophthalmol. Vis. Sci. 2022;63(7):1787 – F0336.

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

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Abstract

Purpose : Photoreceptor cells produce a receptor protein for pigment epithelium-derived factor (PEDF-R), which is encoded by the PNPLA2 gene of the patatin-like phospholipase domain-containing 2 family. PEDF-R is a membrane-linked lipase detected in the inner segments of photoreceptors. We aim to reveal the physiological role of PEDF-R in photoreceptors by characterizing CRISPR Pnpla2 knock-out mouse lines.

Methods : CRISPR-derived Pnpla2 knock-out mouse lines were generated in a C57BL/6 and rd8 free background. RT-PCR was performed from dissected retinas. Mice were evaluated for fundoscopy, electroretinography and angiography. Organs of the thorax were harvested and imaged using a LEICA microscope. Plasma was collected for lipid analyses. Eyes were enucleated and processed for histology, immunofluorescence, confocal microscopy, and transmission electron microscopy.

Results : Pnpla2-/- mice had undetectable retinal Pnpla2 expression levels, enlarged whiter hearts, and lower plasma free fatty acids and triglycerides levels than their Pnpla2+/+ littermate controls. Their retinal pigment epithelial cells accumulated lipid droplets and their photoreceptors were deformed. Fundi of Pnpla2+/- eyes had white spots. The optic nerve area of Pnpla2-/- and Pnpla2+/- mice had an excess of pigment. The a-wave in Pnpla2-/- and Pnpla2+/- mice, and b-wave in Pnpla2+/- mice were attenuated relative to controls. Retinal rhodopsin and opsin gene expression of Pnpla2-/- and Pnpla2+/- were lower than in controls. The immunofluorescent intensities of rhodopsin and opsin antibodies decreased in Pnpla2+/- and Pnpla2-/- photoreceptors relative to controls. The immunofluorescence of PKCα and synaptophysin antibodies (markers for bipolar cells and ribbon synapse) in the Pnpla2+/- retinas were lower than in controls.

Conclusions : Ablation of Pnpla2 in mice causes malformation of photoreceptors and affects photoreceptor performance, identifying PEDF-R as an important component for photoreceptor structure and function. These findings suggest that the absence of PEDF-R in photoreceptor cells interrupts PEDF neurotrophic action, thereby heightening degeneration in the mice.

This abstract was presented at the 2022 ARVO Annual Meeting, held in Denver, CO, May 1-4, 2022, and virtually.

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