IDEAS home Printed from https://ideas.repec.org/a/plo/pone00/0222596.html
   My bibliography  Save this article

The polyether ionophore salinomycin targets multiple cellular pathways to block proliferative vitreoretinopathy pathology

Author

Listed:
  • Alison M Heffer
  • Jacob Proaño
  • Elisa Roztocil
  • Richard P Phipps
  • Steven E Feldon
  • Krystel R Huxlin
  • Patricia J Sime
  • Richard T Libby
  • Collynn F Woeller
  • Ajay E Kuriyan

Abstract

Proliferative vitreoretinopathy (PVR) is characterized by membranes that form in the vitreous cavity and on both surfaces of the retina, which results in the formation of tractional membranes that can cause retinal detachment and intrinsic fibrosis of the retina, leading to retina foreshortening. Currently, there are no pharmacologic therapies that are effective in inhibiting or preventing PVR formation. One of the key aspects of PVR pathogenesis is retinal pigment epithelial (RPE) cell epithelial mesenchymal transition (EMT). Here we show that the polyether ionophore compound salinomycin (SNC) effectively inhibits TGFβ-induced EMT of RPE cells. SNC blocks the activation of TGFβ-induced downstream targets alpha smooth muscle actin (αSMA) and collagen 1 (Col1A1). Additionally, SNC inhibits TGFβ-induced RPE cell migration and contraction. We show that SNC functions to inhibit RPE EMT by targeting both the pTAK1/p38 and Smad2 signaling pathways upon TGFβ stimulation. Additionally, SNC is able to inhibit αSMA and Col1A1 expression in RPE cells that have already undergone TGFβ-induced EMT. Together, these results suggest that SNC could be an effective therapeutic compound in both the prevention and treatment of PVR.

Suggested Citation

  • Alison M Heffer & Jacob Proaño & Elisa Roztocil & Richard P Phipps & Steven E Feldon & Krystel R Huxlin & Patricia J Sime & Richard T Libby & Collynn F Woeller & Ajay E Kuriyan, 2019. "The polyether ionophore salinomycin targets multiple cellular pathways to block proliferative vitreoretinopathy pathology," PLOS ONE, Public Library of Science, vol. 14(9), pages 1-16, September.
  • Handle: RePEc:plo:pone00:0222596
    DOI: 10.1371/journal.pone.0222596
    as

    Download full text from publisher

    File URL: https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0222596
    Download Restriction: no

    File URL: https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0222596&type=printable
    Download Restriction: no

    File URL: https://libkey.io/10.1371/journal.pone.0222596?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    References listed on IDEAS

    as
    1. Zeev Dvashi & Mordechai Goldberg & Orit Adir & Michal Shapira & Ayala Pollack, 2015. "TGF-β1 Induced Transdifferentiation of RPE Cells is Mediated by TAK1," PLOS ONE, Public Library of Science, vol. 10(4), pages 1-16, April.
    Full references (including those not matched with items on IDEAS)

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.

      More about this item

      Statistics

      Access and download statistics

      Corrections

      All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:plo:pone00:0222596. See general information about how to correct material in RePEc.

      If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

      If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

      If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

      For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: plosone (email available below). General contact details of provider: https://journals.plos.org/plosone/ .

      Please note that corrections may take a couple of weeks to filter through the various RePEc services.

      IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.