Fate-Restricted Neural Progenitors in the Mammalian Cerebral Cortex

被引:248
作者
Franco, Santos J.
Gil-Sanz, Cristina
Martinez-Garay, Isabel
Espinosa, Ana
Harkins-Perry, Sarah R.
Ramos, Cynthia
Mueller, Ulrich [1 ]
机构
[1] Scripps Res Inst, Dorris Neurosci Ctr, La Jolla, CA 92037 USA
关键词
INTERMEDIATE PROGENITORS; LAMINAR FATE; STEM-CELLS; NEOCORTEX; NEURONS; MOUSE; CRE; RECOMBINATION; SPECIFICATION; EXPRESSION;
D O I
10.1126/science.1223616
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
During development of the mammalian cerebral cortex, radial glial cells (RGCs) generate layer-specific subtypes of excitatory neurons in a defined temporal sequence, in which lower-layer neurons are formed before upper-layer neurons. It has been proposed that neuronal subtype fate is determined by birthdate through progressive restriction of the neurogenic potential of a common RGC progenitor. Here, we demonstrate that the murine cerebral cortex contains RGC sublineages with distinct fate potentials. Using in vivo genetic fate mapping and in vitro clonal analysis, we identified an RGC lineage that is intrinsically specified to generate only upper-layer neurons, independently of niche and birthdate. Because upper cortical layers were expanded during primate evolution, amplification of this RGC pool may have facilitated human brain evolution.
引用
收藏
页码:746 / 749
页数:4
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