Hwang Ki-Chul, Kim Ji Young, Chang Woochul, Kim Dae-Sung, Lim Soyeon, Kang Sang-Moon, Song Byeong-Wook, Ha Hye-Yeong, Huh Yong Joon, Choi In-Geol, Hwang Dong-Youn, Song Heesang, Jang Yangsoo, Chung Namsik, Kim Sung-Hou, Kim Dong-Wook
Cardiovascular Research Institute, Department of Physiology, and Brain Korea 21 Project for Medical Science, Yonsei University College of Medicine, Seoul 120-752, Korea.
Proc Natl Acad Sci U S A. 2008 May 27;105(21):7467-71. doi: 10.1073/pnas.0802825105. Epub 2008 May 14.
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.
诸如细胞命运等重要的细胞过程可能由多种信号通路精心编排控制,其中许多仍未被充分理解或知晓。由于蛋白激酶是参与调节许多已知信号通路的一大类蛋白质成员,它们可能在平衡多种信号以调节细胞命运中发挥重要作用,因此我们最初在已知的蛋白激酶抑制剂中寻找调节干细胞命运的化学试剂。我们筛选了六个主要蛋白激酶亚家族的41种特征明确的抑制剂,以改变参与干细胞分化的多种信号通路的编排。我们发现其中一些会导致两种干细胞,即大鼠间充质干细胞(MSC)和小鼠胚胎干细胞(ESC)的分化率发生可识别的变化。在众多抑制剂中,我们描述了同一支架化合物异喹啉磺酰胺的两种最有效的衍生物对干细胞分化的影响:大鼠MSC分化为软骨细胞以及小鼠ESC分化为多巴胺能神经元。