Mitotic spindle regulation by Nde1 controls cerebral cortical size

被引:281
作者
Feng, YY [1 ]
Walsh, CA [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Neurol, Beth Israel Deaconess Med Ctr,Howard Hughes Med I, Boston, MA 02115 USA
关键词
D O I
10.1016/j.neuron.2004.09.023
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Ablation of the LIS1-interacting protein Nde1 (formerly mNudE) in mouse produces a small brain (microcephaly), with the most dramatic reduction affecting the cerebral cortex. While cortical lamination is mostly preserved, the mutant cortex has fewer neurons and very thin superficial cortical layers (II to IV). BrdU birthdating revealed retarded and modestly disorganized neuronal migration; however, more dramatic defects on mitotic progression, mitotic orientation, and mitotic chromosome localization in cortical progenitors were observed in Nde1 mutant embryos. The small cerebral cortex seems to reflect both reduced progenitor cell division and altered neuronal cell fates. In vitro analysis demonstrated that Nde1 is essential for centrosome duplication and mitotic spindle assembly. Our data show that mitotic spindle function and orientation are essential for normal development of mammalian cerebral cortex.
引用
收藏
页码:279 / 293
页数:15
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