Tseng Ai-Sun, Engel Felix B, Keating Mark T
Howard Hughes Medical Institute, Department of Cardiology, Children's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA.
Chem Biol. 2006 Sep;13(9):957-63. doi: 10.1016/j.chembiol.2006.08.004.
The maintenance of self-renewal in stem cells appears to be distinct from the induction of proliferation of the terminally differentiated mammalian cardiomyocytes because it is believed that the latter are unable to divide. However, proliferation is a necessary step in both processes. Interestingly, the small molecule 6-bromoindirubin-3'-oxime (BIO) is the first pharmacological agent shown to maintain self-renewal in human and mouse embryonic stem cells. To determine whether a molecule that can maintain stem cell properties can also participate in controlling the proliferative capability of the highly differentiated cardiomyocytes, we examine the effect of BIO in postmitotic cardiac cells. Here, we show that BIO promotes proliferation in mammalian cardiomyocytes. Our demonstration of a second role for BIO suggests that the maintenance of stem cell self-renewal and the induction of proliferation in differentiated cardiomyocytes may share common molecular pathways.
干细胞自我更新的维持似乎与终末分化的哺乳动物心肌细胞增殖的诱导不同,因为人们认为后者无法分裂。然而,增殖在这两个过程中都是必要步骤。有趣的是,小分子6-溴靛玉红-3'-肟(BIO)是第一种被证明能维持人及小鼠胚胎干细胞自我更新的药物。为了确定一种能够维持干细胞特性的分子是否也能参与控制高度分化的心肌细胞的增殖能力,我们研究了BIO对有丝分裂后心脏细胞的影响。在此,我们表明BIO可促进哺乳动物心肌细胞的增殖。我们对BIO第二种作用的证明表明,干细胞自我更新的维持与分化心肌细胞增殖的诱导可能共享共同的分子途径。