July 2019
Volume 60, Issue 9
Open Access
ARVO Annual Meeting Abstract  |   July 2019
Inhibition of VCP structurally and functionally reconstitutes photoreceptor cells in RhP23H organotypic retina cultures
Author Affiliations & Notes
  • Blanca Arango-Gonzalez
    Centre for Ophthalmology, University Eye Hospital Tübingen, Tübingen, Germany
  • Merve Sen
    Centre for Ophthalmology, University Eye Hospital Tübingen, Tübingen, Germany
    Graduate Training Centre of Neuroscience, Eberhard Karls University of Tübingen,, Tübingen, Germany
  • Tsui-Fen Chou
    Department of Pediatrics, Harbor-UCLA Medical Center and Los Angeles Biomedical Research Institute, California, United States
  • Ray Deshaies
    Research, Amgen, Inc., California, United States
  • Sylvia Bolz
    Centre for Ophthalmology, University Eye Hospital Tübingen, Tübingen, Germany
  • Wadood Haq
    Centre for Ophthalmology, University Eye Hospital Tübingen, Tübingen, Germany
  • Marius Ueffing
    Centre for Ophthalmology, University Eye Hospital Tübingen, Tübingen, Germany
  • Footnotes
    Commercial Relationships   Blanca Arango-Gonzalez, None; Merve Sen, None; Tsui-Fen Chou, None; Ray Deshaies, Amgen (E), Cleave Biosciences (I); Sylvia Bolz, None; Wadood Haq, None; Marius Ueffing, None
  • Footnotes
    Support  FFB Grant PPA-0717-0719-RAD; H2020-MSCA-ITN-2016 OcuTher-722717; H2020-EYE-RISK Grant 634479; Pro-Re/Projekt/Ueffing.1-2015; Pro-Re/Projekt/Ueffing.1-2015/17
Investigative Ophthalmology & Visual Science July 2019, Vol.60, 4878. doi:
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      Blanca Arango-Gonzalez, Merve Sen, Tsui-Fen Chou, Ray Deshaies, Sylvia Bolz, Wadood Haq, Marius Ueffing; Inhibition of VCP structurally and functionally reconstitutes photoreceptor cells in RhP23H organotypic retina cultures. Invest. Ophthalmol. Vis. Sci. 2019;60(9):4878.

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

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Abstract

Purpose : Due to high production rates in visual pigment and high metabolic activity, photoreceptor neurons (PN) are especially vulnerable to defects in proteostasis. The structurally misfolded rhodopsin (Rh)P23H exerts excessive stress on rods, causing adRP. The ATPase valosin-containing protein (VCP) acts as a quality control checkpoint of membrane proteins and binds to Rh before its release from the ER. This study evaluated the effect of VCP inhibition in the RhP23H rat in vitro

Methods : Retinal organ cultures from heterozygous RhP23H transgenic rats (SD-Tg(P23H)1Lav, RRRC) with the RPE attached, as previously described (Arango-Gonzalez et al. 2010), were incubated in supplemented serum-free medium and treated either with Eeyarestatin I (EerI) or with ML240. PN survival, as well as functional and structural integrity, was evaluated by cell row quantification, TUNEL assay, high-resolution light microscopy and electron microscopy (EM). One-way ANOVA followed by Tukey’s HSD test was used for statistical analysis. The impact of the treatment on the retinal visual responses was investigated by light stimulation and simultaneous ganglion cell recordings, utilizing multi-electrode arrays (MEA)

Results : The percentage of TUNEL(+) cells in the ONL indicates that VCP inhibition significantly reduced the number of dying cells (EerI: 1,70%±0,39, P<0,001; ML240: 2,23%±0,36, P<0,0001; control: 5,08%±0,41). More importantly, the ONL of EerI and ML240-treated RhP23H retinas contained more cell rows than the controls (EerI: 9,48±0,21, P<0.0222; ML240; 9,49±0,93, P<0.0063; control: 8,08±0,54). VCP inhibition also corrected the aberrant distribution of Rh, arrestin, and transducin in the RhP23H transgenic rat retina, restoring their physiological localization similar to that of the WT phenotype. Ultrastructural analysis by EM confirmed preservation of proper morphology within treated RhP23H rod outer segments (OS) and electrophysiological MEA recordings demonstrated improved responses to light stimulation in the treated RhP23H retina

Conclusions : VCP inhibition strongly rescues degenerating RhP23H rods and preserve the functional properties of the retina, suggesting VCP as a target to treat adRP. Protection correlates with restoration of physiological Rh trafficking to rod OS. This results in improved rod OS ultrastructure as well as an electrophysiological response in treated RhP23H retinas

This abstract was presented at the 2019 ARVO Annual Meeting, held in Vancouver, Canada, April 28 - May 2, 2019.

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