miR-124 regulates adult neurogenesis in the subventricular zone stem cell niche

被引:827
作者
Cheng, Li-Chun [1 ]
Pastrana, Erika [1 ]
Tavazoie, Masoud [2 ]
Doetsch, Fiona [1 ,3 ]
机构
[1] Columbia Univ, Coll Phys & Surg, Dept Pathol & Cell Biol, New York, NY 10027 USA
[2] Columbia Univ, Coll Phys & Surg, Dept Neurosci, New York, NY USA
[3] Columbia Univ, Coll Phys & Surg, Ctr Motor Neuron Biol & Dis, New York, NY USA
基金
美国国家卫生研究院;
关键词
RADIAL GLIAL-CELLS; NEURONAL DIFFERENTIATION; MAMMALIAN BRAIN; SELF-RENEWAL; SPINAL-CORD; MICRORNA; EXPRESSION; SOX9; PRECURSORS; REST;
D O I
10.1038/nn.2294
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The subventricular zone (SVZ) is the largest neurogenic niche in the adult mammalian brain. We found that the brain-enriched microRNA miR-124 is an important regulator of the temporal progression of adult neurogenesis in mice. Knockdown of endogenous miR-124 maintained purified SVZ stem cells as dividing precursors, whereas ectopic expression led to precocious and increased neuron formation. Furthermore, blocking miR-124 function during regeneration led to hyperplasias, followed by a delayed burst of neurogenesis. We identified the SRY-box transcription factor Sox9 as being a physiological target of miR-124 at the transition from the transit amplifying cell to the neuroblast stage. Sox9 overexpression abolished neuronal differentiation, whereas Sox9 knockdown led to increased neuron formation. Thus miR-124-mediated repression of Sox9 is important for progression along the SVZ stem cell lineage to neurons.
引用
收藏
页码:399 / 408
页数:10
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