Department of Chemical and Systems Biology, Stanford University, Stanford, CA 94305, USA.
Science. 2014 Jun 20;344(6190):1384-9. doi: 10.1126/science.1252079.
Mammalian tissue size is maintained by slow replacement of de-differentiating and dying cells. For adipocytes, key regulators of glucose and lipid metabolism, the renewal rate is only 10% per year. We used computational modeling, quantitative mass spectrometry, and single-cell microscopy to show that cell-to-cell variability, or noise, in protein abundance acts within a network of more than six positive feedbacks to permit pre-adipocytes to differentiate at very low rates. This reconciles two fundamental opposing requirements: High cell-to-cell signal variability is needed to generate very low differentiation rates, whereas low signal variability is needed to prevent differentiated cells from de-differentiating. Higher eukaryotes can thus control low rates of near irreversible cell fate decisions through a balancing act between noise and ultrahigh feedback connectivity.
哺乳动物组织的大小由去分化和死亡细胞的缓慢替换来维持。对于脂肪细胞,即葡萄糖和脂质代谢的关键调节者,其更新率仅为每年 10%。我们使用计算建模、定量质谱和单细胞显微镜表明,蛋白质丰度的细胞间变异性或噪声在超过六个正反馈的网络内发挥作用,从而允许前脂肪细胞以非常低的速率分化。这调和了两个基本的对立要求:高细胞间信号变异性是产生非常低的分化率所必需的,而低信号变异性是防止分化细胞去分化所必需的。因此,高等生物可以通过在噪声和超高反馈连接性之间进行平衡来控制低速率的近乎不可逆的细胞命运决定。