IDEAS home Printed from https://ideas.repec.org/a/nat/nature/v476y2011i7359d10.1038_nature10202.html
   My bibliography  Save this article

Induction of human neuronal cells by defined transcription factors

Author

Listed:
  • Zhiping P. Pang

    (Stanford University School of Medicine, 265 Campus Drive)

  • Nan Yang

    (Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, 265 Campus Drive)

  • Thomas Vierbuchen

    (Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, 265 Campus Drive
    Program in Cancer Biology, Stanford University School of Medicine, 265 Campus Drive)

  • Austin Ostermeier

    (Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, 265 Campus Drive
    Program in Cancer Biology, Stanford University School of Medicine, 265 Campus Drive)

  • Daniel R. Fuentes

    (Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, 265 Campus Drive)

  • Troy Q. Yang

    (Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, 265 Campus Drive)

  • Ami Citri

    (Stanford University School of Medicine, 265 Campus Drive)

  • Vittorio Sebastiano

    (Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, 265 Campus Drive)

  • Samuele Marro

    (Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, 265 Campus Drive)

  • Thomas C. Südhof

    (Stanford University School of Medicine, 265 Campus Drive
    Howard Hughes Medical Institute, Stanford University School of Medicine, 265 Campus Drive)

  • Marius Wernig

    (Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, 265 Campus Drive
    Program in Cancer Biology, Stanford University School of Medicine, 265 Campus Drive)

Abstract

Neurons from fibroblasts Three papers in this issue demonstrate the production of functional induced neuronal (iN) cells from human fibroblasts, a procedure that holds great promise for regenerative medicine. Pang et al. show that a combination of the three transcription factors Ascl1 (also known as Mash1), Brn2 (or Pou3f2) and Myt1l greatly enhances the neuronal differentiation of human embryonic stem cells. When combined with the basic helix–loop–helix transcription factor NeuroD1, these factors can also convert fetal and postnatal human fibroblasts into iN cells. Caiazzo et al. use a cocktail of three transcription factors to convert prenatal and adult mouse and human fibroblasts into functional dopaminergic neurons. The three are Mash1, Nurr1 (or Nr4a2) and Lmx1a. Conversion is direct with no reversion to a progenitor cell stage, and it occurs in cells from Parkinson's disease patients as well as from healthy donors. Yoo et al. use an alternative approach. They show that microRNAs can have an instructive role in neural fate determination. Expression of miR-9/9* and miR-124 in human fibroblasts induces their conversion into functional neurons, and the process is facilitated by the addition of some neurogenic transcription factors.

Suggested Citation

  • Zhiping P. Pang & Nan Yang & Thomas Vierbuchen & Austin Ostermeier & Daniel R. Fuentes & Troy Q. Yang & Ami Citri & Vittorio Sebastiano & Samuele Marro & Thomas C. Südhof & Marius Wernig, 2011. "Induction of human neuronal cells by defined transcription factors," Nature, Nature, vol. 476(7359), pages 220-223, August.
  • Handle: RePEc:nat:nature:v:476:y:2011:i:7359:d:10.1038_nature10202
    DOI: 10.1038/nature10202
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/nature10202
    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/nature10202?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. Maria A. Missinato & Sean Murphy & Michaela Lynott & Michael S. Yu & Anaïs Kervadec & Yu-Ling Chang & Suraj Kannan & Mafalda Loreti & Christopher Lee & Prashila Amatya & Hiroshi Tanaka & Chun-Teng Hua, 2023. "Conserved transcription factors promote cell fate stability and restrict reprogramming potential in differentiated cells," Nature Communications, Nature, vol. 14(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:476:y:2011:i:7359:d:10.1038_nature10202. 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.