IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v5y2014i1d10.1038_ncomms6216.html
   My bibliography  Save this article

An authentic imaging probe to track cell fate from beginning to end

Author

Listed:
  • Seung Koo Lee

    (Molecular Imaging Innovations Institute, Weill Cornell Medical College)

  • Luke J. Mortensen

    (Wellman Center for Photomedicine, Massachusetts General Hospital, Harvard Medical School)

  • Charles P. Lin

    (Wellman Center for Photomedicine, Massachusetts General Hospital, Harvard Medical School)

  • Ching-Hsuan Tung

    (Molecular Imaging Innovations Institute, Weill Cornell Medical College)

Abstract

Accurate tracing of cell viability is critical for optimizing delivery methods and evaluating the efficacy and safety of cell therapeutics. A nanoparticle-based cell tracker is developed to image cell fate from live to dead. The particle is fabricated from two types of optically quenched polyelectrolytes, a life indicator and a death indicator, through electrostatic interactions. On incubation with cells, the fabricated bifunctional nanoprobes are taken up efficiently and the first colour is produced by normal intracellular proteolysis, reflecting the healthy status of the cells. Depending on the number of coated layers, the signal can persist for several replication cycles. However, as the cells begin dying, the second colour appears quickly to reflect the new cell status. Using this chameleon-like cell tracker, live cells can be distinguished from apoptotic and necrotic cells instantly and definitively.

Suggested Citation

  • Seung Koo Lee & Luke J. Mortensen & Charles P. Lin & Ching-Hsuan Tung, 2014. "An authentic imaging probe to track cell fate from beginning to end," Nature Communications, Nature, vol. 5(1), pages 1-8, December.
  • Handle: RePEc:nat:natcom:v:5:y:2014:i:1:d:10.1038_ncomms6216
    DOI: 10.1038/ncomms6216
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/ncomms6216
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/ncomms6216?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
    ---><---

    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:nat:natcom:v:5:y:2014:i:1:d:10.1038_ncomms6216. 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.

    We have no bibliographic references for this item. You can help adding them by using 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: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    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.