中段
生物
胞质分裂
细胞生物学
劈理沟
有丝分裂
干细胞
大脑皮层
驱动蛋白
神经发生
神经上皮细胞
神经干细胞
解剖
细胞分裂
微管
遗传学
神经科学
细胞
作者
K Janisch,Vita M. Vock,Michael S. Fleming,Ayushma Shrestha,Cynthia M. Grimsley‐Myers,Bareza A. Rasoul,Sarah A. Neale,Timothy D. Cupp,Jason M. Kinchen,Karel F. Liem,Noelle D. Dwyer
出处
期刊:Development
[The Company of Biologists]
日期:2013-10-31
卷期号:140 (23): 4672-4682
被引量:55
摘要
Mammalian neuroepithelial stem cells divide using a polarized form of cytokinesis, which is not well understood. The cytokinetic furrow cleaves the cell by ingressing from basal to apical, forming the midbody at the apical membrane. The midbody mediates abscission by recruiting many factors, including the Kinesin-6 family member Kif20b. In developing embryos, Kif20b mRNA is most highly expressed in neural stem/progenitor cells. A loss-of-function mutant in Kif20b, magoo, was found in a forward genetic screen. magoo has a small cerebral cortex, with reduced production of progenitors and neurons, but preserved layering. In contrast to other microcephalic mouse mutants, mitosis and cleavage furrows of cortical stem cells appear normal in magoo. However, apical midbodies show changes in number, shape and positioning relative to the apical membrane. Interestingly, the disruption of abscission does not appear to result in binucleate cells, but in apoptosis. Thus, Kif20b is required for proper midbody organization and abscission in polarized cortical stem cells and has a crucial role in the regulation of cerebral cortex growth.
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