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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >The Notch pathway mediates expansion of a progenitor pool and neuronal differentiation in adult neural progenitor cells after stroke.
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The Notch pathway mediates expansion of a progenitor pool and neuronal differentiation in adult neural progenitor cells after stroke.

机译:Notch通路介导中风后成人神经祖细胞中祖细胞池的扩增和神经元分化。

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摘要

Molecular mechanisms by which stroke increases neurogenesis have not been fully investigated. Using neural progenitor cells isolated from the subventricular zone (SVZ) of the adult rat subjected to focal cerebral ischemia, we investigated the Notch pathway in regulating proliferation and differentiation of adult neural progenitor cells after stroke. During proliferation of neural progenitor cells, ischemic neural progenitor cells exhibited substantially increased levels of Notch, Notch intracellular domain (NICD), and hairy enhancer of split (Hes) 1, which was associated with a significant increase of proliferating cells. Blockage of the Notch pathway by short interfering ribonucleic acid (siRNA) against Notch or a gamma secretase inhibitor significantly reduced Notch, NICD and Hes1 expression and cell proliferation induced by stroke. During differentiation of neural progenitor cells, Notch and Hes1 expression was downregulated in ischemic neural progenitor cells, which was coincident with a significant increase of neuronal population. Inhibition of the Notch pathway with a gamma secretase inhibitor further substantially increased neurons, but did not alter astrocyte population in ischemic neural progenitor cells. These data suggest that the Notch signaling pathway mediates adult SVZ neural progenitor cell proliferation and differentiation after stroke.
机译:中风增加神经发生的分子机制尚未得到充分研究。使用从经历局灶性脑缺血的成年大鼠脑室下区(SVZ)分离的神经祖细胞,我们研究了Notch通路在中风后调节成年神经祖细胞增殖和分化的过程。在神经祖细胞的增殖过程中,缺血性神经祖细胞的Notch,Notch细胞内结构域(NICD)和毛分裂增强剂(Hes)1的水平显着增加,这与增殖细胞的显着增加有关。 Notch短干扰核糖核酸(siRNA)对抗Notch或γ分泌酶抑制剂可阻断Notch通路,从而显着降低Notch,NICD和Hes1表达以及中风诱导的细胞增殖。在神经祖细胞分化过程中,Notch和Hes1表达在缺血性神经祖细胞中被下调,这与神经元种群的显着增加相吻合。用γ分泌酶抑制剂抑制Notch途径进一步实质性增加了神经元,但并未改变缺血性神经祖细胞中的星形胶质细胞群。这些数据表明,Notch信号通路介导了中风后成人SVZ神经祖细胞的增殖和分化。

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