June 2020
Volume 61, Issue 7
Open Access
ARVO Annual Meeting Abstract  |   June 2020
Pink1-mitophagy and Nrf2-stress response mediated novel mitochondrial retrograde signaling affects RPE structure and function
Author Affiliations & Notes
  • Sayantan Datta
    Johns Hopkins Medicine, Baltimore, Maryland, United States
  • Marisol Cano
    Johns Hopkins Medicine, Baltimore, Maryland, United States
  • Hiromi Sesaki
    Johns Hopkins Medicine, Baltimore, Maryland, United States
  • James T Handa
    Johns Hopkins Medicine, Baltimore, Maryland, United States
  • Footnotes
    Commercial Relationships   Sayantan Datta, None; Marisol Cano, None; Hiromi Sesaki, None; James Handa, None
  • Footnotes
    Support  K99EY029010
Investigative Ophthalmology & Visual Science June 2020, Vol.61, 3185. doi:
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    • Get Citation

      Sayantan Datta, Marisol Cano, Hiromi Sesaki, James T Handa; Pink1-mitophagy and Nrf2-stress response mediated novel mitochondrial retrograde signaling affects RPE structure and function. Invest. Ophthalmol. Vis. Sci. 2020;61(7):3185.

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

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Abstract

Purpose : In AMD, RPE cells show structural and functional heterogeneity, where death resistant RPE undergoing EMT exist alongside normal and dying RPE. The molecular mechanism underlying this heterogeneity is unknown. In a novel finding, we have shown that impairment of Pink1 mitophagy directly leads to RPE EMT in an Nrf2 dependent manner and impairment of both Pink1 and Nrf2 causes RPE death. Here we try to delineate the signaling mechanism using RNA seq and characterize the molecular and functional relevance in vivo using Pink1KO mice.

Methods : ARPE-19 and iPS-RPE cells after 6 days of transfection with the following siRNAs-scramble, Nrf2, Pink1 and Nrf2-Pink1 - were tested for: EMT - using Vimentin staining, expression of EMT TFs Snail1 and Zeb1, and cell viability using Calcein-AM. RNA seq (HiSeq) of the 4 cell types was performed and pathways analyzed using DAVID. mtROS and AKT inhibitors were used to mechanistically connect them to EMT. RPE from C57BL6J, Nrf2KO and Pink1KO mice were examined for evidence of structural abnormality and mitophagy and EMT were biochemically investigated in Pink1KO mice using qPCR and western blots and functional tests (ERG and OKN) were done. Pink1 and Snail distribution in the RPE were assessed using IHC in AMD globes.

Results : In human AMD samples, RPE over drusen showed higher Snail and lower Pink1 expression (fig1a,b). Pink1KO mice had dysmorphic RPE and poor visual acuity compared to C57 mice (fig1c,d). Western blot revealed lower pParkin and LC3b2 indicating impaired mitophagy with an increase in Vimentin in Pink1KO RPE (Fig1e). ARPE-19 & iPS-RPE cells showed cell elongation with Pink1KD. Pink1KD also had lower parkin and LC3b2 levels in mt fraction suggesting impaired mitophagy and 2-fold increased Zeb1 and significant increase in mtROS(Fig2a-c). The double KD cells showed morphological reversal of EMT but poor cell survivability (Fig2d). RNA seq revealed upregulation of PI3k AKT signaling in Pink1KD cells and EMT was rescued by treatments with AKT inhibitor (A6730) and a novel dendrimer attached NAC (Fig2e).

Conclusions : Pink1 loss caused Nrf2 dependent adaptive EMT and loss of both Pink1 and Nrf2 cells look normal but are death prone. Pink1 loss triggered a retrograde signaling cascade mediated by mtROS, Nrf2 and AKT. These results thus identify novel therapeutic targets for restoring RPE functionality in AMD.

This is a 2020 ARVO Annual Meeting abstract.

 

 

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