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Disabled 1的表达抑制神经干细胞中的星形胶质细胞分化。

Expression of Disabled 1 suppresses astroglial differentiation in neural stem cells.

作者信息

Kwon Il-Sun, Cho Sung-Kuk, Kim Min-Ji, Tsai Ming-Jer, Mitsuda Noriaki, Suh-Kim Haeyoung, Lee Young-Don

机构信息

Department of Anatomy, School of Medicine, Ajou University, Suwon, 443-749, South Korea.

出版信息

Mol Cell Neurosci. 2009 Jan;40(1):50-61. doi: 10.1016/j.mcn.2008.08.012. Epub 2008 Sep 18.

Abstract

Disabled 1 (Dab1), a cytoplasmic adaptor protein expressed predominantly in the CNS, transduces a Reelin-initiated signaling that controls neuronal migration and positioning during brain development. To determine the role of Dab1 in neural stem cell (NSC) differentiation, we established a culture of neurospheres derived from the embryonic forebrain of the Dab1(-/-) mice, yotari. Differentiating Dab1(-/-) neurospheres exhibited a higher expression of GFAP, an astrocytic marker, at the expense of neuronal markers. Under Dab1-deficient condition, the expression of NeuroD, a transcription factor for neuronal differentiation, was decreased and the JAK-STAT pathway was evidently increased during differentiation of NSC, suggesting the possible involvement of Dab1 in astrocyte differentiation via JAK-STAT pathway. Notably, expression of neural and glial markers and the level of JAK-STAT signaling molecules were not changed in differentiating NSC by Reelin treatment, indicating that differentiation of NSC is Reelin-independent. Immunohistochemical analyses showed a decrease in the number of neurons and an increase in the number of GFAP-positive cells in developing yotari brains. Our results suggest that Dab1 participates in the differentiation of NSCs into a specific cell lineage, thereby maintaining a balance between neurogenesis and gliogenesis.

摘要

Disabled 1(Dab1)是一种主要在中枢神经系统中表达的胞质衔接蛋白,它转导一种由Reelin启动的信号,该信号在大脑发育过程中控制神经元的迁移和定位。为了确定Dab1在神经干细胞(NSC)分化中的作用,我们建立了源自Dab1基因敲除小鼠(yotari)胚胎前脑的神经球培养体系。分化中的Dab1基因敲除神经球显示,作为星形胶质细胞标志物的GFAP表达较高,而神经元标志物的表达则相应减少。在缺乏Dab1的条件下,神经元分化转录因子NeuroD的表达降低,并且在神经干细胞分化过程中JAK-STAT信号通路明显增强,这表明Dab1可能通过JAK-STAT信号通路参与星形胶质细胞的分化。值得注意的是,通过Reelin处理,分化中的神经干细胞的神经和胶质标志物表达以及JAK-STAT信号分子水平均未发生变化,这表明神经干细胞的分化不依赖于Reelin。免疫组织化学分析显示,在发育中的yotari小鼠大脑中,神经元数量减少,而GFAP阳性细胞数量增加。我们的结果表明,Dab1参与神经干细胞向特定细胞谱系的分化,从而维持神经发生和胶质发生之间的平衡。

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