IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v7y2016i1d10.1038_ncomms11958.html
   My bibliography  Save this article

Microvesicles provide a mechanism for intercellular communication by embryonic stem cells during embryo implantation

Author

Listed:
  • Laura M. Desrochers

    (Cornell University)

  • François Bordeleau

    (Meinig School of Biomedical Engineering, Cornell University)

  • Cynthia A. Reinhart-King

    (Meinig School of Biomedical Engineering, Cornell University)

  • Richard A. Cerione

    (Cornell University
    Cornell University)

  • Marc A. Antonyak

    (Cornell University)

Abstract

Communication between the inner cell mass (ICM) and the trophoblast layer of the blastocyst is known to occur, but its functional consequences on early developmental events is unclear. Here we demonstrate that embryonic stem (ES) cells derived from the ICM generate and shed microvesicles (MVs), a major class of extracellular vesicles (EVs), which influence trophoblast behaviour during the implantation process. The MV cargo proteins laminin and fibronectin interact with integrins along the surfaces of the trophoblasts, triggering the activation of two signalling kinases, JNK and FAK, and stimulating trophoblast migration. We further show that injecting MVs isolated from ES cells into blastocysts results in an increase in their implantation efficiency. Thus, these findings highlight a unique mechanism by which ES cells communicate with trophoblasts within the blastocyst to increase their ability to migrate into the uterus, thereby promoting one of the earliest and most important steps during pregnancy.

Suggested Citation

  • Laura M. Desrochers & François Bordeleau & Cynthia A. Reinhart-King & Richard A. Cerione & Marc A. Antonyak, 2016. "Microvesicles provide a mechanism for intercellular communication by embryonic stem cells during embryo implantation," Nature Communications, Nature, vol. 7(1), pages 1-11, September.
  • Handle: RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms11958
    DOI: 10.1038/ncomms11958
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/ncomms11958
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/ncomms11958?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:7:y:2016:i:1:d:10.1038_ncomms11958. 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.