IDEAS home Printed from https://ideas.repec.org/a/nat/nature/v449y2007i7160d10.1038_nature06129.html
   My bibliography  Save this article

Generation of functional multipotent adult stem cells from GPR125+ germline progenitors

Author

Listed:
  • Marco Seandel

    (Howard Hughes Medical Institute, and
    and)

  • Daylon James

    (Howard Hughes Medical Institute, and)

  • Sergey V. Shmelkov

    (Howard Hughes Medical Institute, and)

  • Ilaria Falciatori

    (Howard Hughes Medical Institute, and)

  • Jiyeon Kim

    (Howard Hughes Medical Institute, and)

  • Sai Chavala

    (Howard Hughes Medical Institute, and)

  • Douglas S. Scherr

    (Weill Cornell Medical College, New York 10065, USA)

  • Fan Zhang

    (Howard Hughes Medical Institute, and)

  • Richard Torres

    (Regeneron Pharmaceuticals, Tarrytown, New York 10591, USA)

  • Nicholas W. Gale

    (Regeneron Pharmaceuticals, Tarrytown, New York 10591, USA)

  • George D. Yancopoulos

    (Regeneron Pharmaceuticals, Tarrytown, New York 10591, USA)

  • Andrew Murphy

    (Regeneron Pharmaceuticals, Tarrytown, New York 10591, USA)

  • David M. Valenzuela

    (Regeneron Pharmaceuticals, Tarrytown, New York 10591, USA)

  • Robin M. Hobbs

    (Cancer Biology and Genetics Program, Memorial Sloan-Kettering Cancer Center, New York 10065, USA
    Cancer Genetics Program, Beth Israel Deaconess Cancer Center, Harvard Medical School, Boston, Massachusetts 02115, USA)

  • Pier Paolo Pandolfi

    (Cancer Biology and Genetics Program, Memorial Sloan-Kettering Cancer Center, New York 10065, USA
    Cancer Genetics Program, Beth Israel Deaconess Cancer Center, Harvard Medical School, Boston, Massachusetts 02115, USA)

  • Shahin Rafii

    (Howard Hughes Medical Institute, and)

Abstract

Stem cells make their mark Adult stem cells are an attractive alternative to embryonic stem cells for therapeutic use. As yet there is no standard method for obtaining such cells from adults and priming them to form different tissues, but a new system that generates large numbers of stem cells from the adult testicle shows promise. It makes use of a novel marker, an orphan receptor known as GPR125, found on the surface of spermatogonial stem cells. The use of specialized feeder cells to support stem cell growth allows stem cells once destined for spermatogenesis to become multipotent. This work also provides clues as to the minimal requirements for multipotency in adult cells.

Suggested Citation

  • Marco Seandel & Daylon James & Sergey V. Shmelkov & Ilaria Falciatori & Jiyeon Kim & Sai Chavala & Douglas S. Scherr & Fan Zhang & Richard Torres & Nicholas W. Gale & George D. Yancopoulos & Andrew Mu, 2007. "Generation of functional multipotent adult stem cells from GPR125+ germline progenitors," Nature, Nature, vol. 449(7160), pages 346-350, September.
  • Handle: RePEc:nat:nature:v:449:y:2007:i:7160:d:10.1038_nature06129
    DOI: 10.1038/nature06129
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/nature06129
    File Function: Abstract
    Download Restriction: Access to the full text of the articles in this series is restricted.

    File URL: https://libkey.io/10.1038/nature06129?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
    ---><---

    As the access to this document is restricted, you may want to search for a different version of it.

    Citations

    Citations are extracted by the CitEc Project, subscribe to its RSS feed for this item.
    as


    Cited by:

    1. Elena Spina & Julia Simundza & Angela Incassati & Anupama Chandramouli & Matthias C. Kugler & Ziyan Lin & Alireza Khodadadi-Jamayran & Christine J. Watson & Pamela Cowin, 2022. "Gpr125 is a unifying hallmark of multiple mammary progenitors coupled to tumor latency," Nature Communications, Nature, vol. 13(1), pages 1-17, December.

    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:nature:v:449:y:2007:i:7160:d:10.1038_nature06129. 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.