Cdk4/CyclinD1 Overexpression in Neural Stem Cells Shortens G1, Delays Neurogenesis, and Promotes the Generation and Expansion of Basal Progenitors

被引:432
作者
Lange, Christian [1 ,2 ,3 ]
Huttner, Wieland B. [3 ]
Calegari, Federico [1 ,2 ,3 ]
机构
[1] Tech Univ Dresden, Fac Med, DFG Res Ctr, D-01307 Dresden, Germany
[2] Tech Univ Dresden, Fac Med, Cluster Excellence Regenerat Therapies Dresden, D-01307 Dresden, Germany
[3] Max Planck Inst Mol Cell Biol & Genet, D-01307 Dresden, Germany
关键词
CYCLIN-DEPENDENT KINASES; FIBROBLAST-GROWTH-FACTOR; NEURONAL DIFFERENTIATION; RNA INTERFERENCE; CEREBRAL-CORTEX; EXIT; INHIBITION; INDUCTION; EVOLUTION; MIGRATION;
D O I
10.1016/j.stem.2009.05.026
中图分类号
Q813 [细胞工程];
学科分类号
摘要
During mouse embryonic development, neural progenitors lengthen the G1 phase of the cell cycle and this has been suggested to be a cause, rather than a consequence, of neurogenesis. To investigate whether G1 lengthening alone may cause the switch of cortical progenitors from proliferation to neurogenesis, we manipulated the expression of cdk/cyclin complexes and found that cdk4/cyclinD1 overexpression prevents G1 lengthening without affecting cell growth, cleavage plane, or cell cycle synchrony with interkinetic nuclearmigration. Specifically, overexpression of cdk4/cyclinD1 inhibited neurogenesis while increasing the generation and expansion of basal ( intermediate) progenitors, resulting in a thicker subventricular zone and larger surface area of the postnatal cortex originating from cdk4/cyclinD1-transfected progenitors. Conversely, lengthening of G1 by cdk4/cyclinD1-RNAi displayed the opposite effects. Thus, G1 lengthening is necessary and sufficient to switch neural progenitors to neurogenesis, and overexpression of cdk4/cyclinD1 can be used to increase progenitor expansion and, perhaps, cortical surface area.
引用
收藏
页码:320 / 331
页数:12
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