Direct reprogramming of fibroblasts into neural stem cells by defined factors.

Han DW, Tapia N, Hermann A, Hemmer K, Höing S, Araúzo-Bravo MJ, Zaehres H, Wu G, Frank S, Moritz S, Greber B, Yang JH, Lee HT, Schwamborn JC, Storch A, Schöler HR

Forschungsartikel (Zeitschrift) | Peer reviewed

Zusammenfassung

Recent studies have shown that defined sets of transcription factors can directly reprogram differentiated somatic cells to a different differentiated cell type without passing through a pluripotent state, but the restricted proliferative and lineage potential of the resulting cells limits the scope of their potential applications. Here we show that a combination of transcription factors (Brn4/Pou3f4, Sox2, Klf4, c-Myc, plus E47/Tcf3) induces mouse fibroblasts to directly acquire a neural stem cell identity-which we term as induced neural stem cells (iNSCs). Direct reprogramming of fibroblasts into iNSCs is a gradual process in which the donor transcriptional program is silenced over time. iNSCs exhibit cell morphology, gene expression, epigenetic features, differentiation potential, and self-renewing capacity, as well as in vitro and in vivo functionality similar to those of wild-type NSCs. We conclude that differentiated cells can be reprogrammed directly into specific somatic stem cell types by defined sets of specific transcription factors.

Details zur Publikation

FachzeitschriftCell Stem Cell
Jahrgang / Bandnr. / Volume10
Ausgabe / Heftnr. / Issue4
Seitenbereich465-472
StatusVeröffentlicht
Veröffentlichungsjahr2012
Sprache, in der die Publikation verfasst istEnglisch
DOI10.1016/j.stem.2012.02.021
StichwörterInduced Pluripotent Stem Cells; Cell Dedifferentiation; Mice; Transcription Factors; Antigens Differentiation; Neural Stem Cells; Animals; Fibroblasts; Gene Expression Regulation; Induced Pluripotent Stem Cells; Cell Dedifferentiation; Mice; Transcription Factors; Antigens Differentiation; Neural Stem Cells; Animals; Fibroblasts; Gene Expression Regulation

Autor*innen der Universität Münster

Schöler, Hans R.
Max-Planck-Institut für Molekulare Biomedizin
Schwamborn, Jens
Institut für Zellbiologie