Literature DB >> 16932739

De-differentiation of mouse interfollicular keratinocytes by the embryonic transcription factor Oct-4.

Katie L Grinnell1, Baoli Yang, Richard L Eckert, Jackie R Bickenbach.   

Abstract

The embryonic transcription factor Oct-4 is often referred to as the master regulator of the undifferentiated state. Although its role in maintaining embryonic stem (ES) cell pluripotency is well established, its ability to directly reprogram committed somatic cells is not well defined. Using transient transfection, we tested its ability to revert mouse interfollicular epidermal basal keratinocytes to a more ES cell-like state. We found that the Oct-4-transfected keratinocytes expressed the Oct-4 target genes, Sox-2, Nanog, undifferentiated transcription factor 1 (Utf1), and Rex-1. We also noted an increase in developmental potential caused by Oct-4, with the transfected cells able to differentiate into neuronal cells when exposed to neuroectodermal differentiation medium. Control-transfected keratinocytes were unable to respond to the medium, and remained as keratinocytes. These findings suggest that Oct-4 may be the master regulator of the pluripotent state and demonstrate that differentiated somatic cells can be reverted into more developmentally potent cells through the use of a single factor. The latter finding has great implications for therapeutic cell-replacement applications using cells from easily accessible adult tissues, such as the skin.

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Year:  2006        PMID: 16932739     DOI: 10.1038/sj.jid.5700531

Source DB:  PubMed          Journal:  J Invest Dermatol        ISSN: 0022-202X            Impact factor:   8.551


  15 in total

Review 1.  Advances in reprogramming somatic cells to induced pluripotent stem cells.

Authors:  Minal Patel; Shuying Yang
Journal:  Stem Cell Rev Rep       Date:  2010-09       Impact factor: 5.739

2.  Embryonic stem cell factors undifferentiated transcription factor-1 (UFT-1) and reduced expression protein-1 (REX-1) are widely expressed in human skin and may be involved in cutaneous differentiation but not in stem cell fate determination.

Authors:  Christina M Reinisch; Michael Mildner; Peter Petzelbauer; Johannes Pammer
Journal:  Int J Exp Pathol       Date:  2011-03-29       Impact factor: 1.925

Review 3.  Biochemistry of epidermal stem cells.

Authors:  Richard L Eckert; Gautam Adhikary; Sivaprakasam Balasubramanian; Ellen A Rorke; Mohan C Vemuri; Shayne E Boucher; Jackie R Bickenbach; Candace Kerr
Journal:  Biochim Biophys Acta       Date:  2012-07-20

Review 4.  Lung cancer stem cells and low-intensity laser irradiation: a potential future therapy?

Authors:  Anine M Crous; Heidi Abrahamse
Journal:  Stem Cell Res Ther       Date:  2013       Impact factor: 6.832

5.  Human immature dental pulp stem cells' contribution to developing mouse embryos: production of human/mouse preterm chimaeras.

Authors:  S A Siqueira da Fonseca; S Abdelmassih; T de Mello Cintra Lavagnolli; R C Serafim; E J Clemente Santos; C Mota Mendes; V de Souza Pereira; C E Ambrosio; M A Miglino; J A Visintin; R Abdelmassih; A Kerkis; I Kerkis
Journal:  Cell Prolif       Date:  2009-02-24       Impact factor: 6.831

6.  Skin keratinocytes pre-treated with embryonic stem cell-conditioned medium or BMP4 can be directed to an alternative cell lineage.

Authors:  K L Grinnell; J R Bickenbach
Journal:  Cell Prolif       Date:  2007-10       Impact factor: 6.831

Review 7.  Epidermal stem cells in skin homeostasis and cutaneous carcinomas.

Authors:  S Aznar Benitah
Journal:  Clin Transl Oncol       Date:  2007-12       Impact factor: 3.405

8.  Rat alveolar type I cells proliferate, express OCT-4, and exhibit phenotypic plasticity in vitro.

Authors:  Robert F Gonzalez; Lennell Allen; Leland G Dobbs
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2009-08-28       Impact factor: 5.464

9.  Molecular mechanisms of induced pluripotency.

Authors:  I A Muchkaeva; E B Dashinimaev; V V Terskikh; Y V Sukhanov; A V Vasiliev
Journal:  Acta Naturae       Date:  2012-01       Impact factor: 1.845

10.  Human skin keratinocytes can be reprogrammed to express neuronal genes and proteins after a single treatment with decitabine.

Authors:  Jackie R Bickenbach; Ann Tomanek-Chalkley; Susan Wiechert; Michael C Winter
Journal:  Biores Open Access       Date:  2013-06
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