Institut de Biologie de l'École Normale Supérieure (IBENS), Paris Sciences et Lettres (PSL) Research University, Paris F-75005, France.
CNRS, UMR 8197, Paris F-75005, France.
Science. 2017 Nov 10;358(6364):803-806. doi: 10.1126/science.aan8311. Epub 2017 Oct 5.
Cell division and differentiation depend on massive and rapid organelle remodeling. The mitotic oscillator, centered on the cyclin-dependent kinase 1-anaphase-promoting complex/cyclosome (CDK1-APC/C) axis, spatiotemporally coordinates this reorganization in dividing cells. Here we discovered that nondividing cells could also implement this mitotic clocklike regulatory circuit to orchestrate subcellular reorganization associated with differentiation. We probed centriole amplification in differentiating mouse-brain multiciliated cells. These postmitotic progenitors fine-tuned mitotic oscillator activity to drive the orderly progression of centriole production, maturation, and motile ciliation while avoiding the mitosis commitment threshold. Insufficient CDK1 activity hindered differentiation, whereas excessive activity accelerated differentiation yet drove postmitotic progenitors into mitosis. Thus, postmitotic cells can redeploy and calibrate the mitotic oscillator to uncouple cytoplasmic from nuclear dynamics for organelle remodeling associated with differentiation.
细胞分裂和分化依赖于大量和快速的细胞器重塑。有丝分裂振荡器以细胞周期蛋白依赖性激酶 1-后期促进复合物/环体(CDK1-APC/C)轴为中心,在分裂细胞中对这种重组进行时空协调。在这里,我们发现非分裂细胞也可以执行这种有丝分裂时钟样调节回路,以协调与分化相关的亚细胞重排。我们探测了分化中的小鼠脑多纤毛细胞中的中心体扩增。这些有丝分裂后祖细胞微调有丝分裂振荡器的活性,以驱动中心体产生、成熟和运动纤毛的有序进行,同时避免有丝分裂的承诺阈值。CDK1 活性不足会阻碍分化,而活性过高会加速分化,但会使有丝分裂后祖细胞进入有丝分裂。因此,有丝分裂后的细胞可以重新配置和校准有丝分裂振荡器,以解耦与分化相关的细胞器重塑的细胞质和核动力学。