生物
细胞生物学
神经球
神经干细胞
神经发生
神经突
细胞分化
星形胶质细胞
神经的
胶质纤维酸性蛋白
干细胞
免疫学
神经科学
生物化学
成体干细胞
中枢神经系统
免疫组织化学
体外
基因
作者
Yun Hee Kim,Jee-In Chung,Hyun Goo Woo,Yi‐Sook Jung,Soo‐Hwan Lee,Chang‐Hyun Moon,Haeyoung Suh‐Kim,Eun Joo Baik
出处
期刊:Stem Cells
[Oxford University Press]
日期:2010-08-31
卷期号:28 (10): 1816-1828
被引量:64
摘要
Neuronal precursor cells (NPCs) are temporally regulated and have the ability to proliferate and differentiate into mature neurons, oligodendrocytes, and astrocytes in the presence of growth factors (GFs). In the present study, the role of the Jak pathway in brain development was investigated in NPCs derived from neurosphere cultures using Jak2 and Jak3 small interfering RNAs and specific inhibitors. Jak2 inhibition profoundly decreased NPC proliferation, preventing further differentiation into neurons and glial cells. However, Jak3 inhibition induced neuronal differentiation accompanied by neurite growth. This phenomenon was due to the Jak3 inhibition-mediated induction of neurogenin (Ngn)2 and NeuroD in NPCs. Jak3 inhibition induced NPCs to differentiate into scattered neurons and increased the expression of Tuj1, microtubule associated protein 2 (MAP2), Olig2, and neuroglial protein (NG)2, but decreased glial fibrillary acidic protein (GFAP) expression, with predominant neurogenesis/polydendrogenesis compared with astrogliogenesis. Therefore, Jak2 may be important for NPC proliferation and maintenance, whereas knocking-down of Jak3 signaling is essential for NPC differentiation into neurons and oligodendrocytes but does not lead to astrocyte differentiation. These results suggest that NPC proliferation and differentiation are differentially regulated by the Jak pathway.
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