空间组织的IGF1-mTOR信号控制人类前脑原始体F ate通过协调的转录和翻译程序
Kadia Lisst1,2, Da Huo1,2, Stephen M Eacker1,3,2
1Neuroregeneration and Stem Cell Programs, Institute for Cell Engineering, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
bioRxiv : the preprint server for biology
|November 24, 2025
概括
一种新的IGF1信号通路通过控制基因翻译来调节人类前脑前科细胞. 这种副膜机制将利基信号与细胞输出相结合,支持神经发育和弹性.
科学领域:
- 神经科学是一个神经科学.
- 发展生物学 发展生物学
- 干细胞生物学 干细胞生物学
背景情况:
- 人类前脑前代细胞的发育依赖于内在的基因和利基信号.
- 这些线索之间的相互作用尚未完全理解.
- 在前脑发育过程中,FOXG1+神经前体细胞 (NPC) 是至关重要的.
研究的目的:
- 调查胰岛素样生长因子1 (IGF1) 信号在人类前脑原生细胞调节中的作用.
- 阐明利基信号影响NPC身份和功能的机制.
- 了解神经发育中转录和翻译控制之间的相互作用.
主要方法:
- 利用多能干细胞衍生前脑模型.
- 雇佣了核糖体分析和5'UTR报告员测定.
- 分析了包括PI3K-AKT-mTOR和MEK-ERK在内的信号通路.
主要成果:
- 确定了一个空间有组织的,偏IGF1信号架构调节人类FOXG1+NPCs.
- 证明IGF1促进了原生细胞的增殖,克隆扩张和组织生长.
- 揭示了mTOR信号选择性地增强神经发育转录的翻译,包括GSX1.
结论:
- 发现了一种涉及空间限制IGF1-mTOR信号的人类特异性调节机制.
- 这一途径将利基信号与翻译输出集成在一起,以保持原始体身份和生物合成能力.
- 这些发现提供了对发育性和与自闭症谱系障碍的潜在联系的见解.
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