Late Origin of Glia-Restricted Progenitors in the Developing Mouse Cerebral Cortex

被引:60
作者
Costa, Marcos R. [1 ]
Bucholz, Oliver [1 ]
Schroeder, Timm [1 ]
Goetz, Magdalena [1 ,2 ]
机构
[1] Natl Res Ctr Environm & Hlth, Helmholtz Zentrum Munchen, Inst Stem Cell Res, D-85764 Neuherberg, Germany
[2] Univ Munich, Inst Physiol, Dept Physiol Genom, D-80336 Munich, Germany
关键词
clonal analysis; cortical development; gliogenesis; neurogenesis; video microscopy; NEURAL STEM-CELLS; CORTICAL NEUROGENESIS; FATE SPECIFICATION; NERVOUS-SYSTEM; PRECURSOR CELL; IN-VITRO; NEURONS; LINEAGES; GENERATION; DISPERSION;
D O I
10.1093/cercor/bhp046
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In order to unravel the molecular determinants of cell fate, it is important to understand when fate restriction occurs during brain development. Lineage analysis suggested that bi- or multipotent progenitors persist into late developmental stages in some central nervous system regions, whereas most progenitor cells in the cerebral cortex appeared to be restrained to generate only a single cell type already at early stages. Here we discuss this previous work and present new data demonstrating that cortical progenitors generating exclusively glial cells appear late in development. In utero transduction of cortical progenitors at early and mid-neurogenesis using a combination of replication-defective retroviral vectors encoding different fluorescent proteins indicated that the early developing cortex is devoid of glia-restricted progenitors, although these are frequent during mid- and late neurogenesis. Clonal analyses in vitro using retroviral vectors and live cell tracking by video time-lapse microscopy confirmed these findings, revealing that the early developing cortex harbors 2 main progenitor types: neuron-restricted and bipotent (neuron-glial) progenitors. The latter are responsible for the generation of glial-restricted progenitors at mid- and late neurogenesis.
引用
收藏
页码:I135 / I143
页数:9
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