成纤维细胞生长因子(FGF)对细胞外调节蛋白激酶1/2(Erk1/2)信号级联的刺激,会触发多能胚胎干细胞从自我更新状态向分化状态的转变。
FGF stimulation of the Erk1/2 signalling cascade triggers transition of pluripotent embryonic stem cells from self-renewal to lineage commitment.
作者信息
Kunath Tilo, Saba-El-Leil Marc K, Almousailleakh Marwa, Wray Jason, Meloche Sylvain, Smith Austin
机构信息
Centre Development in Stem Cell Biology, Institute for Stem Cell Research, School of Biological Sciences, University of Edinburgh, Edinburgh, UK.
出版信息
Development. 2007 Aug;134(16):2895-902. doi: 10.1242/dev.02880.
Pluripotent embryonic stem (ES) cells must select between alternative fates of self-replication and lineage commitment during continuous proliferation. Here, we delineate the role of autocrine production of fibroblast growth factor 4 (Fgf4) and associated activation of the Erk1/2 (Mapk3/1) signalling cascade. Fgf4 is the major stimulus activating Erk in mouse ES cells. Interference with FGF or Erk activity using chemical inhibitors or genetic ablations does not impede propagation of undifferentiated ES cells. Instead, such manipulations restrict the ability of ES cells to commit to differentiation. ES cells lacking Fgf4 or treated with FGF receptor inhibitors resist neural and mesodermal induction, and are refractory to BMP-induced non-neural differentiation. Lineage commitment potential of Fgf4-null cells is restored by provision of FGF protein. Thus, FGF enables rather than antagonises the differentiation activity of BMP. The key downstream role of Erk signalling is revealed by examination of Erk2-null ES cells, which fail to undergo either neural or mesodermal differentiation in adherent culture, and retain expression of pluripotency markers Oct4, Nanog and Rex1. These findings establish that Fgf4 stimulation of Erk1/2 is an autoinductive stimulus for naïve ES cells to exit the self-renewal programme. We propose that the Erk cascade directs transition to a state that is responsive to inductive cues for germ layer segregation. Consideration of Erk signalling as a primary trigger that potentiates lineage commitment provides a context for reconciling disparate views on the contribution of FGF and BMP pathways during germ layer specification in vertebrate embryos.
多能胚胎干细胞在持续增殖过程中必须在自我复制和谱系定向的不同命运之间做出选择。在此,我们阐述了成纤维细胞生长因子4(Fgf4)的自分泌产生以及相关的细胞外信号调节激酶1/2(Erk1/2,即丝裂原活化蛋白激酶3/1,Mapk3/1)信号级联激活的作用。Fgf4是激活小鼠胚胎干细胞中Erk的主要刺激因子。使用化学抑制剂或基因敲除干扰FGF或Erk活性并不妨碍未分化胚胎干细胞的增殖。相反,这种操作限制了胚胎干细胞进行分化的能力。缺乏Fgf4或用FGF受体抑制剂处理的胚胎干细胞抵抗神经和中胚层诱导,并且对骨形态发生蛋白(BMP)诱导的非神经分化具有抗性。通过提供FGF蛋白可恢复Fgf4基因敲除细胞的谱系定向潜能。因此,FGF促进而非拮抗BMP的分化活性。通过对Erk2基因敲除的胚胎干细胞进行检测揭示了Erk信号的关键下游作用,这些细胞在贴壁培养中无法进行神经或中胚层分化,并保留多能性标志物Oct4、Nanog和Rex1的表达。这些发现表明,Fgf4对Erk1/2的刺激是幼稚胚胎干细胞退出自我更新程序的自诱导刺激。我们提出,Erk级联反应引导细胞过渡到一种对胚层分离诱导信号有反应的状态。将Erk信号视为增强谱系定向的主要触发因素,为调和关于脊椎动物胚胎胚层特化过程中FGF和BMP信号通路贡献的不同观点提供了一个背景。