June 2015
Volume 56, Issue 7
ARVO Annual Meeting Abstract  |   June 2015
Primary Cilia Regulates the Polarization and Maturation of hiPSC-RPE through PKC-delta Activation
Author Affiliations & Notes
  • Qin Wan
    SERPD, NEI/NIH, Bethesda, MD
  • Juliet Hartford
    OSCTR, NEI/NIH, Bethesda, MD
  • Omar Memon
    SERPD, NEI/NIH, Bethesda, MD
  • Vladimir Khristov
    OSCTR, NEI/NIH, Bethesda, MD
  • Janine Davis
    OSCTR, NEI/NIH, Bethesda, MD
  • Sheldon S Miller
    SERPD, NEI/NIH, Bethesda, MD
  • Kapil Bharti
    OSCTR, NEI/NIH, Bethesda, MD
  • Footnotes
    Commercial Relationships Qin Wan, None; Juliet Hartford, None; Omar Memon, None; Vladimir Khristov, None; Janine Davis, None; Sheldon Miller, None; Kapil Bharti, None
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science June 2015, Vol.56, 2345. doi:
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      Qin Wan, Juliet Hartford, Omar Memon, Vladimir Khristov, Janine Davis, Sheldon S Miller, Kapil Bharti; Primary Cilia Regulates the Polarization and Maturation of hiPSC-RPE through PKC-delta Activation. Invest. Ophthalmol. Vis. Sci. 2015;56(7 ):2345.

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

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Purpose: Retinal pigment epithelium (RPE), a ciliated monolayer of cells situated adjacent to retinal photoreceptors, is critical for photoreceptor survival and function. Similar to most somatic cells, RPE contains a primary cilium during development. But the role of primary cilium in human RPE development remains largely unknown. The goal of this study is to explore the function and underlying signaling pathway of primary cilium in RPE development and maturation.

Methods: Human induced pluripotent stem cell derived RPE (iPSC-RPE) were grown on semi-permeable transwells to generate a confluent monolayer. Primary cilia in iPSC-RPE were manipulated using a cilia inducer aphidicolin or cilia function inhibitor HPI-4. Electrophysiology recordings were performed to measure RPE transepithelial potential (TEP) and total tissue resistance (Rt). Immunocytochemistry was used to determine the proper polarization and morphogenesis of iPSC-RPE.

Results: Six weeks treatment with aphidicolin increased baseline TEP by up to three-folds; it also dramatically enhanced RPE responses to two physiologically relevant stimuli (apical low K+ and ATP). In contrast, suppression of cilium growth with HPI-4 significantly reduced the baseline TEP/Rt and blocked the low K+ and ATP responses, suggesting that cilium function is crucial for the polarization and maturation of RPE monolayer. Pharmacological inhibition of PKC-δ, a polarization inducing kinase, with rottlerin attenuated the effect of aphidicolin in a dose-dependent manner; similar inhibitory effects were also observed with another PKC-δ blocker Go6850. Positive immunostaining for the active phosphorylated form of PKC-δ and Phospho-MLC further confirmed that aphidicolin-induced polarization in the RPE monolayer acted through PKC-δ pathway.

Conclusions: These results indicate that the development of primary cilium in iPSC-RPE has a direct and dramatic impact on RPE monolayer polarization and maturation through modulation of PKC-δ pathway. Manipulation of this pathway can help differentiate and mature RPE cells for stem cell-based therapies.


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