细胞生物学
Notch信号通路
下调和上调
电池极性
极性(国际关系)
神经干细胞
细胞生长
信号转导
生物
祖细胞
化学
细胞
干细胞
生物化学
基因
作者
Jiawen Xu,Xin Deng,Aihong Gu,Yuqun Cai,Yunyun Huang,Wen Zhang,Yiqing Zhang,Wenyu Wen,Yunli Xie
出处
期刊:Cell Reports
[Cell Press]
日期:2023-06-23
卷期号:42 (7): 112677-112677
被引量:8
标识
DOI:10.1016/j.celrep.2023.112677
摘要
Polarity proteins regulate the proliferation and differentiation of neural progenitors to generate neurons during brain development through multiple signaling pathways. However, how cell polarity couples the signaling pathways remains unclear. Here, we show that coiled-coil domain-containing protein 85c (Ccdc85c) interacts with the polarity protein Par3 to regulate the proliferation of radial glial cells (RGCs) via phase separation coupled to percolation (PSCP). We find that the interaction with Ccdc85c relieves the intramolecular auto-inhibition of Par3, which leads to PSCP of Par3. Downregulation of Ccdc85c causes RGC differentiation. Importantly, the open conformation of Par3 facilitates the recruitment of the Notch regulator Numb to the Par3 condensates, which might prevent the attenuation of Notch activity to maintain RGC proliferation. Furthermore, ectopic activation of Notch signaling rescues RGC proliferation defects caused by the downregulation of Ccdc85c. These results suggest that Ccdc85c-mediated PSCP of Par3 regulates Notch signaling to control RGC proliferation during brain development.
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