Literature DB >> 19404413

Reprogramming somatic cells to their embryonic state.

Valerie Horsley1, Elaine Fuchs.   

Abstract

Embryonic stem (ES) cells have the capacity to form every type of cell in our adult bodies due to their pluripotency. The prospective use of ES cells in regenerative therapies for human diseases such as Parkinson's disease and diabetes has raised the interest in identifying the mechanisms that allow these cells to maintain pluripotent fate and differentiate along many lineages. However, ethical questions regarding the use of human eggs andor embryos for medical research have limited the ability of scientists to develop therapies with human ES cells. Three recent papers in Nature and Cell Stem Cell have revealed novel methods of reprogramming somatic cells into cells with the same pluripotent potential as ES cells via the expression of only four transcription factors. These scientific advances illuminate the mechanisms that drive pluripotent fate in embryonic cells. In addition, by giving scientists a model to study ES-like cells that are not derived from embryos, these newly identified models have the potential to progress therapies for regenerative medicine.

Entities:  

Year:  2007        PMID: 19404413      PMCID: PMC2639841          DOI: 10.2976/1.2757614

Source DB:  PubMed          Journal:  HFSP J        ISSN: 1955-205X


  30 in total

Review 1.  Transcriptional regulation and transformation by Myc proteins.

Authors:  Sovana Adhikary; Martin Eilers
Journal:  Nat Rev Mol Cell Biol       Date:  2005-08       Impact factor: 94.444

2.  Overexpression of NANOG in human ES cells enables feeder-free growth while inducing primitive ectoderm features.

Authors:  Henia Darr; Yoav Mayshar; Nissim Benvenisty
Journal:  Development       Date:  2006-03       Impact factor: 6.868

3.  Transcriptional regulation of nanog by OCT4 and SOX2.

Authors:  David J Rodda; Joon-Lin Chew; Leng-Hiong Lim; Yuin-Han Loh; Bei Wang; Huck-Hui Ng; Paul Robson
Journal:  J Biol Chem       Date:  2005-04-27       Impact factor: 5.157

4.  Klf4 is a transcription factor required for establishing the barrier function of the skin.

Authors:  J A Segre; C Bauer; E Fuchs
Journal:  Nat Genet       Date:  1999-08       Impact factor: 38.330

5.  Klf4 cooperates with Oct3/4 and Sox2 to activate the Lefty1 core promoter in embryonic stem cells.

Authors:  Yuhki Nakatake; Nobutaka Fukui; Yuko Iwamatsu; Shinji Masui; Kadue Takahashi; Rika Yagi; Kiyohito Yagi; Jun-Ichi Miyazaki; Ryo Matoba; Minoru S H Ko; Hitoshi Niwa
Journal:  Mol Cell Biol       Date:  2006-09-05       Impact factor: 4.272

6.  Nuclear reprogramming of somatic cells after fusion with human embryonic stem cells.

Authors:  Chad A Cowan; Jocelyn Atienza; Douglas A Melton; Kevin Eggan
Journal:  Science       Date:  2005-08-26       Impact factor: 47.728

Review 7.  Regulatory networks in embryo-derived pluripotent stem cells.

Authors:  Michele Boiani; Hans R Schöler
Journal:  Nat Rev Mol Cell Biol       Date:  2005-11       Impact factor: 94.444

8.  Octamer and Sox elements are required for transcriptional cis regulation of Nanog gene expression.

Authors:  Takao Kuroda; Masako Tada; Hiroshi Kubota; Hironobu Kimura; Shin-ya Hatano; Hirofumi Suemori; Norio Nakatsuji; Takashi Tada
Journal:  Mol Cell Biol       Date:  2005-03       Impact factor: 4.272

9.  Murine embryonic stem cell differentiation is promoted by SOCS-3 and inhibited by the zinc finger transcription factor Klf4.

Authors:  Yanjun Li; Jeanette McClintick; Li Zhong; Howard J Edenberg; Mervin C Yoder; Rebecca J Chan
Journal:  Blood       Date:  2004-09-09       Impact factor: 22.113

10.  Generation of germline-competent induced pluripotent stem cells.

Authors:  Keisuke Okita; Tomoko Ichisaka; Shinya Yamanaka
Journal:  Nature       Date:  2007-06-06       Impact factor: 49.962

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