Protein Phosphatase 4 and Smek Complex Negatively Regulate Par3 and Promote Neuronal Differentiation of Neural Stem/Progenitor Cells

被引:36
|
作者
Lyu, Jungmook [1 ,2 ]
Kim, Hee-Ryang [1 ]
Yamamoto, Vicky [2 ]
Choi, Si Ho [2 ]
Wei, Zong [2 ]
Joo, Choun-Ki [1 ]
Lu, Wange [2 ]
机构
[1] Catholic Univ Korea, Catholic Inst Visual Sci, Dept Ophthalmol & Visual Sci, Coll Med, Seoul 137040, South Korea
[2] Univ So Calif, Keck Sch Med, Eli & Edythe Broad Ctr Regenerat Med & Stem Cell, Dept Biochem & Mol Biol, Los Angeles, CA 90042 USA
来源
CELL REPORTS | 2013年 / 5卷 / 03期
基金
新加坡国家研究基金会; 美国国家卫生研究院;
关键词
NEUROBLAST ASYMMETRIC DIVISIONS; STEM-CELLS; CONSERVED PROTEIN; NEUROGENESIS; POLARITY; NOTCH; PHOSPHORYLATION; NEOCORTEX;
D O I
10.1016/j.celrep.2013.09.034
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Neural progenitor cells (NPCs) are multipotent cells that can self-renew and differentiate into neurons and glial cells. However, mechanisms that control their fate decisions are poorly understood. Here, we show that Smek1, a regulatory subunit of the serine/threonine protein phosphatase PP4, promotes neuronal differentiation and suppresses the proliferative capacity of NPCs. We identify the cell polarity protein Par3, a negative regulator of neuronal differentiation, as a Smek1 substrate and demonstrate that Smek1 suppresses its activity. We also show that Smek1, which is predominantly nuclear in NPCs, is excluded from the nucleus during mitosis, allowing it to interact with cortical/cytoplasmic Par3 and mediate its dephosphorylation by the catalytic subunit PP4c. These results identify the PP4/Smek1 complex as a key regulator of neurogenesis.
引用
收藏
页码:593 / 600
页数:8
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