| Literature DB >> 25363410 |
Da-Woon Jung1, Young J Hong, Soo-Yeon Kim, Woong-Hee Kim, Shinae Seo, Jung-Eun Lee, Haihong Shen, Yong-Chul Kim, Darren R Williams.
Abstract
Patient-derived cell transplantation is an attractive therapy for regenerative medicine. However, this requires effective strategies to reliably differentiate patient cells into clinically useful cell types. Herein, we report the discovery that 5-nitro-5'hydroxy-indirubin-3'oxime (5'-HNIO) is a novel inducer of cell transdifferentiation. 5'-HNIO induced muscle transdifferentiation into adipogenic and osteogenic cells. 5'-HNIO was shown to inhibit aurora kinase A, which is a known cell fate regulator. 5'-HNIO produced a favorable level of transdifferentiation compared to other aurora kinase inhibitors and induced transdifferentiation across cell lineage boundaries. Significantly, 5'-HNIO treatment produced direct transdifferentiation without up-regulating potentially oncogenic induced pluripotent stem cell (iPSC) reprogramming factors. Thus, our results demonstrate that 5'-HNIO is an attractive molecular tool for cell transdifferentiation and cell fate research.Entities:
Keywords: Aurora kinase; Cell transdifferentiation; Chemical biology; Indirubin; Small molecules
Mesh:
Substances:
Year: 2014 PMID: 25363410 DOI: 10.1002/ardp.201400223
Source DB: PubMed Journal: Arch Pharm (Weinheim) ISSN: 0365-6233 Impact factor: 3.751