Department of Chemical and Systems Biology, Stanford University, Stanford, CA 94305, USA.
Mol Cell. 2012 Jan 27;45(2):196-209. doi: 10.1016/j.molcel.2011.11.023. Epub 2011 Dec 28.
Growth factors activate Ras, PI3K, and other signaling pathways. It is not well understood how these signals are translated by individual cells into a decision to proliferate or differentiate. Here, using single-cell image analysis of nerve growth factor (NGF)-stimulated PC12 cells, we identified a two-dimensional phospho-ERK (pERK)-phospho-AKT (pAKT) response map with a curved boundary that separates differentiating from proliferating cells. The boundary position remained invariant when different stimuli were used or upstream signaling components perturbed. We further identified Rasa2 as a negative feedback regulator that links PI3K to Ras, placing the stochastically distributed pERK-pAKT signals close to the decision boundary. This allows for uniform NGF stimuli to create a subpopulation of cells that differentiates with each cycle of proliferation. Thus, by linking a complex signaling system to a simpler intermediate response map, cells gain unique integration and control capabilities to balance cell number expansion with differentiation.
生长因子激活 Ras、PI3K 和其他信号通路。目前还不清楚这些信号如何被单个细胞转化为增殖或分化的决定。在这里,我们使用单细胞图像分析神经生长因子(NGF)刺激的 PC12 细胞,鉴定了一个二维磷酸化 ERK(pERK)-磷酸化 AKT(pAKT)反应图,其边界呈曲线形,将分化细胞与增殖细胞分开。当使用不同的刺激物或干扰上游信号成分时,边界位置保持不变。我们进一步鉴定出 Rasa2 是一个负反馈调节剂,它将 PI3K 与 Ras 连接起来,将随机分布的 pERK-pAKT 信号靠近决策边界。这使得均匀的 NGF 刺激能够创建一个具有每个增殖周期分化的细胞亚群。因此,通过将复杂的信号系统与更简单的中间反应图联系起来,细胞获得了独特的整合和控制能力,以平衡细胞数量的扩张与分化。