Neural Stem Cells to Cerebral Cortex: Emerging Mechanisms Regulating Progenitor Behavior and Productivity

被引:58
作者
Dwyer, Noelle D. [1 ]
Chen, Bin [2 ]
Chou, Shen-Ju [3 ]
Hippenmeyer, Simon [4 ]
Nguyen, Laurent [5 ]
Ghashghaei, H. Troy [6 ]
机构
[1] Univ Virginia, Sch Med, Dept Cell Biol, POB 800732, Charlottesville, VA 22908 USA
[2] Univ Calif Santa Cruz, Dept Mol Cell & Dev Biol, Santa Cruz, CA 95064 USA
[3] Acad Sinica, Inst Cellular & Organism Biol, Taipei 115, Taiwan
[4] IST Austria, Dev Neurobiol, A-3400 Klosterneuburg, Austria
[5] Univ Liege, CHU Sart Tilman, GIGA Neurosci, B-4000 Liege, Belgium
[6] North Carolina State Univ, Coll Vet Med, Dept Mol Biomed Sci, Raleigh, NC 27607 USA
基金
美国国家卫生研究院;
关键词
cortical development; Cux2; cytokinesis; Fezf2; Kif20b; Lhx2; lineage; MADM; microcephaly; mouse; neurogenesis; Sp2; UPR; SUBCORTICAL PROJECTION NEURONS; UNFOLDED PROTEIN RESPONSE; ASYMMETRIC INHERITANCE; CORTICAL NEUROGENESIS; SPINDLE ORIENTATION; PYRAMIDAL NEURONS; PRIMARY CILIUM; BASAL PROCESS; RADIAL GLIA; MIDBODY;
D O I
10.1523/JNEUROSCI.2359-16.2016
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
This review accompanies a 2016 SFN mini-symposium presenting examples of current studies that address a central question: How do neural stem cells (NSCs) divide in different ways to produce heterogeneous daughter types at the right time and in proper numbers to build a cerebral cortex with the appropriate size and structure? We will focus on four aspects of corticogenesis: cytokinesis events that follow apical mitoses of NSCs; coordinating abscission with delamination from the apical membrane; timing of neurogenesis and its indirect regulation through emergence of intermediate progenitors; and capacity of single NSCs to generate the correct number and laminar fate of cortical neurons. Defects in these mechanisms can cause microcephaly and other brain malformations, and understanding them is critical to designing diagnostic tools and preventive and corrective therapies.
引用
收藏
页码:11394 / 11401
页数:8
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