| Literature DB >> 18480249 |
Ki-Chul Hwang1, Ji Young Kim, Woochul Chang, Dae-Sung Kim, Soyeon Lim, Sang-Moon Kang, Byeong-Wook Song, Hye-Yeong Ha, Yong Joon Huh, In-Geol Choi, Dong-Youn Hwang, Heesang Song, Yangsoo Jang, Namsik Chung, Sung-Hou Kim, Dong-Wook Kim.
Abstract
Important cellular processes such as cell fate are likely to be controlled by an elaborate orchestration of multiple signaling pathways, many of which are still not well understood or known. Because protein kinases, the members of a large family of proteins involved in modulating many known signaling pathways, are likely to play important roles in balancing multiple signals to modulate cell fate, we focused our initial search for chemical reagents that regulate stem cell fate among known inhibitors of protein kinases. We have screened 41 characterized inhibitors of six major protein kinase subfamilies to alter the orchestration of multiple signaling pathways involved in differentiation of stem cells. We found that some of them cause recognizable changes in the differentiation rates of two types of stem cells, rat mesenchymal stem cells (MSCs) and mouse embryonic stem cells (ESCs). Among many, we describe the two most effective derivatives of the same scaffold compound, isoquinolinesulfonamide, on the stem cell differentiation: rat MSCs to chondrocytes and mouse ESCs to dopaminergic neurons.Entities:
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Year: 2008 PMID: 18480249 PMCID: PMC2396687 DOI: 10.1073/pnas.0802825105
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205