Programmed Cell Death in Neurodevelopment

被引:170
|
作者
Yamaguchi, Yoshifumi [1 ,2 ]
Miura, Masayuki [1 ,3 ]
机构
[1] Univ Tokyo, Grad Sch Pharmaceut Sci, Dept Genet, Bunkyo Ku, Tokyo 1130033, Japan
[2] Japan Sci & Technol Agcy, PRESTO Precursory Res Embryon Sci & Technol, Chiyoda Ku, Tokyo 1020076, Japan
[3] Japan Sci & Technol Agcy, CREST, Chiyoda Ku, Tokyo 1020076, Japan
关键词
SEXUALLY DIMORPHIC BRAIN; CEREBRAL CORTICAL SIZE; CENTRAL-NERVOUS-SYSTEM; NEURAL PROLIFERATION; CASPASE ACTIVITY; APOPTOTIC CELLS; CHICK-EMBRYO; IN-VIVO; POSTEMBRYONIC DEVELOPMENT; GALACTOSIDASE ACTIVITY;
D O I
10.1016/j.devcel.2015.01.019
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Programmed cell death (PCD) is an evolutionarily conserved contributor to nervous system development In the vertebrate peripheral nervous system, PCD is the basis of the neurotrophic theory, whereby cell death results from a surplus of neurons relative to target and competition for neurotrophic factors. In addition to stochastic cell death, PCD can be intrinsically determined by cell lineage or position and timing in both invertebrate and vertebrate central nervous systems. The underlying PCD molecular mechanisms include intrinsic transcription factor cascades and regulators of competence/susceptibility to cell death. Here, we provide a framework for understanding neural PCD from its regulation to its functions.
引用
收藏
页码:478 / 490
页数:13
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